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2024-03-29 16:11:14, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_032446               7689 bp    mRNA    linear   PRI 29-JUN-2013
DEFINITION  Homo sapiens multiple EGF-like-domains 10 (MEGF10), transcript
            variant 1, mRNA.
ACCESSION   NM_032446
VERSION     NM_032446.2  GI:181336652
KEYWORDS    RefSeq.
SOURCE      Homo sapiens (human)
  ORGANISM  Homo sapiens
            Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
            Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
            Catarrhini; Hominidae; Homo.
REFERENCE   1  (bases 1 to 7689)
  AUTHORS   Sherva,R., Tripodis,Y., Bennett,D.A., Chibnik,L.B., Crane,P.K., de
            Jager,P.L., Farrer,L.A., Saykin,A.J., Shulman,J.M. and Green,R.C.
  CONSRTM   The GENAROADS Consortium, and The Alzheimer's Disease Neuroimaging
            Initiative
  TITLE     Genome-wide association study of the rate of cognitive decline in
            Alzheimer's disease
  JOURNAL   Alzheimers Dement (2013) In press
   PUBMED   23535033
  REMARK    Publication Status: Available-Online prior to print
REFERENCE   2  (bases 1 to 7689)
  AUTHORS   Lauc,G., Huffman,J.E., Pucic,M., Zgaga,L., Adamczyk,B., Muzinic,A.,
            Novokmet,M., Polasek,O., Gornik,O., Kristic,J., Keser,T.,
            Vitart,V., Scheijen,B., Uh,H.W., Molokhia,M., Patrick,A.L.,
            McKeigue,P., Kolcic,I., Lukic,I.K., Swann,O., van Leeuwen,F.N.,
            Ruhaak,L.R., Houwing-Duistermaat,J.J., Slagboom,P.E., Beekman,M.,
            de Craen,A.J., Deelder,A.M., Zeng,Q., Wang,W., Hastie,N.D.,
            Gyllensten,U., Wilson,J.F., Wuhrer,M., Wright,A.F., Rudd,P.M.,
            Hayward,C., Aulchenko,Y., Campbell,H. and Rudan,I.
  TITLE     Loci associated with N-glycosylation of human immunoglobulin G show
            pleiotropy with autoimmune diseases and haematological cancers
  JOURNAL   PLoS Genet. 9 (1), E1003225 (2013)
   PUBMED   23382691
REFERENCE   3  (bases 1 to 7689)
  AUTHORS   Boyden,S.E., Mahoney,L.J., Kawahara,G., Myers,J.A., Mitsuhashi,S.,
            Estrella,E.A., Duncan,A.R., Dey,F., DeChene,E.T.,
            Blasko-Goehringer,J.M., Bonnemann,C.G., Darras,B.T., Mendell,J.R.,
            Lidov,H.G., Nishino,I., Beggs,A.H., Kunkel,L.M. and Kang,P.B.
  TITLE     Mutations in the satellite cell gene MEGF10 cause a recessive
            congenital myopathy with minicores
  JOURNAL   Neurogenetics 13 (2), 115-124 (2012)
   PUBMED   22371254
  REMARK    GeneRIF: Megf10 is required for preserving the undifferentiated,
            proliferative potential of satellite cells, myogenic precursors
            that regenerate skeletal muscle in response to injury or disease.
            GeneRIF: Mutations in MEGF10 cause a recessive congenital myopathy
            with minicores and suggest satellite cell dysfunction as the
            pathogenic mechanism
REFERENCE   4  (bases 1 to 7689)
  AUTHORS   Logan,C.V., Lucke,B., Pottinger,C., Abdelhamed,Z.A., Parry,D.A.,
            Szymanska,K., Diggle,C.P., van Riesen,A., Morgan,J.E., Markham,G.,
            Ellis,I., Manzur,A.Y., Markham,A.F., Shires,M., Helliwell,T.,
            Scoto,M., Hubner,C., Bonthron,D.T., Taylor,G.R., Sheridan,E.,
            Muntoni,F., Carr,I.M., Schuelke,M. and Johnson,C.A.
  TITLE     Mutations in MEGF10, a regulator of satellite cell myogenesis,
            cause early onset myopathy, areflexia, respiratory distress and
            dysphagia (EMARDD)
  JOURNAL   Nat. Genet. 43 (12), 1189-1192 (2011)
   PUBMED   22101682
  REMARK    GeneRIF: Mutations in MEGF10, a regulator of satellite cell
            myogenesis, cause early onset myopathy, areflexia, respiratory
            distress and dysphagia (EMARDD)
            Publication Status: Online-Only
REFERENCE   5  (bases 1 to 7689)
  AUTHORS   Yun,L., Gu,Y. and Hou,Y.
  TITLE     No association between schizophrenia and rs27388 of the MEGF10 gene
            in Chinese case-control sample
  JOURNAL   Psychiatry Res 186 (2-3), 467-468 (2011)
   PUBMED   20813413
  REMARK    GeneRIF: The results of this study suggested that no association
            between schizophrenia and rs27388 of the MEGF10 gene in Chinese
            case-control sample.
REFERENCE   6  (bases 1 to 7689)
  AUTHORS   Singh,T.D., Park,S.Y., Bae,J.S., Yun,Y., Bae,Y.C., Park,R.W. and
            Kim,I.S.
  TITLE     MEGF10 functions as a receptor for the uptake of amyloid-beta
  JOURNAL   FEBS Lett. 584 (18), 3936-3942 (2010)
   PUBMED   20828568
  REMARK    GeneRIF: MEGF10 is involved in the uptake of amyloid-beta peptide
            (Abeta42) in the brain.
REFERENCE   7  (bases 1 to 7689)
  AUTHORS   Chen,X., Wang,X., Chen,Q., Williamson,V., van den Oord,E.,
            Maher,B.S., O'Neill,F.A., Walsh,D. and Kendler,K.S.
  TITLE     MEGF10 association with schizophrenia
  JOURNAL   Biol. Psychiatry 63 (5), 441-448 (2008)
   PUBMED   18179784
  REMARK    GeneRIF: In expression studies, MEGF10 had higher expression levels
            in the affected than the unaffected (p = .015). Schizophrenia
            patients with a 1/1 genotype at rs27388 had higher expressions than
            those patients with 1/2 and 2/2 genotypes (p = .0008).
            GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   8  (bases 1 to 7689)
  AUTHORS   Suzuki,E. and Nakayama,M.
  TITLE     MEGF10 is a mammalian ortholog of CED-1 that interacts with
            clathrin assembly protein complex 2 medium chain and induces large
            vacuole formation
  JOURNAL   Exp. Cell Res. 313 (17), 3729-3742 (2007)
   PUBMED   17643423
  REMARK    GeneRIF: An interaction between MEGF10 and clathrin assembly
            protein complex 2 medium chain (AP50), a component of
            clathrin-coated pits was identified.
REFERENCE   9  (bases 1 to 7689)
  AUTHORS   Suzuki,E. and Nakayama,M.
  TITLE     The mammalian Ced-1 ortholog MEGF10/KIAA1780 displays a novel
            adhesion pattern
  JOURNAL   Exp. Cell Res. 313 (11), 2451-2464 (2007)
   PUBMED   17498693
  REMARK    GeneRIF: Human MEGF10 is an ortholog of Ced1.
REFERENCE   10 (bases 1 to 7689)
  AUTHORS   Hamon,Y., Trompier,D., Ma,Z., Venegas,V., Pophillat,M.,
            Mignotte,V., Zhou,Z. and Chimini,G.
  TITLE     Cooperation between engulfment receptors: the case of ABCA1 and
            MEGF10
  JOURNAL   PLoS ONE 1, E120 (2006)
   PUBMED   17205124
  REMARK    GeneRIF: in a system of forced expression by transfection, MEGF10
            function can be modulated by the ATP binding cassette transporter
            ABCA1, ortholog to CED-7
            Publication Status: Online-Only
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from DA240513.1, AB058676.1,
            AC008682.6 and AC010424.9.
            This sequence is a reference standard in the RefSeqGene project.
            On Apr 10, 2008 this sequence version replaced gi:14192942.
            
            Summary: This gene encodes a member of the multiple epidermal
            growth factor-like domains protein family. The encoded protein
            plays a role in cell adhesion, motility and proliferation, and is a
            critical mediator of apoptotic cell phagocytosis as well as
            amyloid-beta peptide uptake in the brain. Expression of this gene
            may be associated with schizophrenia, and mutations in this gene
            are a cause of early-onset myopathy, areflexia, respiratory
            distress, and dysphagia (EMARDD) as well as congenital myopathy
            with minicores. Alternatively spliced transcript variants have been
            observed for this gene. [provided by RefSeq, Apr 2012].
            
            Transcript Variant: This variant (1) represents the longer
            transcript. Variants 1 and 2 encode the same protein.
            
            Sequence Note: This RefSeq record was created from transcript and
            genomic sequence data to make the sequence consistent with the
            reference genome assembly. The genomic coordinates used for the
            transcript record were based on transcript alignments.
            
            Publication Note:  This RefSeq record includes a subset of the
            publications that are available for this gene. Please see the Gene
            record to access additional publications.
            
            ##Evidence-Data-START##
            Transcript exon combination :: BC152478.1, AB058676.1 [ECO:0000332]
            RNAseq introns              :: mixed/partial sample support
                                           ERS025081, ERS025082 [ECO:0000350]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-190               DA240513.1         1-190
            191-1475            AB058676.1         32-1316
            1476-1492           AC008682.6         91149-91165         c
            1493-3748           AB058676.1         1334-3589
            3749-7689           AC010424.9         26200-30140
FEATURES             Location/Qualifiers
     source          1..7689
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="5"
                     /map="5q33"
     gene            1..7689
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /note="multiple EGF-like-domains 10"
                     /db_xref="GeneID:84466"
                     /db_xref="HGNC:29634"
                     /db_xref="HPRD:14384"
                     /db_xref="MIM:612453"
     exon            1..293
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       68
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:372558738"
     variation       80
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:189260424"
     variation       160
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146523995"
     variation       190
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2032834"
     misc_feature    204..206
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /note="upstream in-frame stop codon"
     exon            294..344
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       297
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:79967765"
     exon            345..478
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       356
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:4620069"
     CDS             363..3785
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /note="multiple epidermal growth factor-like domains
                     protein 10"
                     /codon_start=1
                     /product="multiple epidermal growth factor-like domains
                     protein 10 precursor"
                     /protein_id="NP_115822.1"
                     /db_xref="GI:14192943"
                     /db_xref="CCDS:CCDS4142.1"
                     /db_xref="GeneID:84466"
                     /db_xref="HGNC:29634"
                     /db_xref="HPRD:14384"
                     /db_xref="MIM:612453"
                     /translation="
MVISLNSCLSFICLLLCHWIGTASPLNLEDPNVCSHWESYSVTVQESYPHPFDQIYYTSCTDILNWFKCTRHRVSYRTAYRHGEKTMYRRKSQCCPGFYESGEMCVPHCADKCVHGRCIAPNTCQCEPGWGGTNCSSACDGDHWGPHCTSRCQCKNGALCNPITGACHCAAGFRGWRCEDRCEQGTYGNDCHQRCQCQNGATCDHVTGECRCPPGYTGAFCEDLCPPGKHGPQCEQRCPCQNGGVCHHVTGECSCPSGWMGTVCGQPCPEGRFGKNCSQECQCHNGGTCDAATGQCHCSPGYTGERCQDECPVGTYGVLCAETCQCVNGGKCYHVSGACLCEAGFAGERCEARLCPEGLYGIKCDKRCPCHLENTHSCHPMSGECACKPGWSGLYCNETCSPGFYGEACQQICSCQNGADCDSVTGKCTCAPGFKGIDCSTPCPLGTYGINCSSRCGCKNDAVCSPVDGSCTCKAGWHGVDCSIRCPSGTWGFGCNLTCQCLNGGACNTLDGTCTCAPGWRGEKCELPCQDGTYGLNCAERCDCSHADGCHPTTGHCRCLPGWSGVHCDSVCAEGRWGPNCSLPCYCKNGASCSPDDGICECAPGFRGTTCQRICSPGFYGHRCSQTCPQCVHSSGPCHHITGLCDCLPGFTGALCNEVCPSGRFGKNCAGICTCTNNGTCNPIDRSCQCYPGWIGSDCSQPCPPAHWGPNCIHTCNCHNGAFCSAYDGECKCTPGWTGLYCTQRCPLGFYGKDCALICQCQNGADCDHISGQCTCRTGFMGRHCEQKCPSGTYGYGCRQICDCLNNSTCDHITGTCYCSPGWKGARCDQAGVIIVGNLNSLSRTSTALPADSYQIGAIAGIIILVLVVLFLLALFIIYRHKQKGKESSMPAVTYTPAMRVVNADYTISGTLPHSNGGNANSHYFTNPSYHTLTQCATSPHVNNRDRMTVTKSKNNQLFVNLKNVNPGKRGPVGDCTGTLPADWKHGGYLNELGAFGLDRSYMGKSLKDLGKNSEYNSSNCSLSSSENPYATIKDPPVLIPKSSECGYVEMKSPARRDSPYAEINNSTSANRNVYEVEPTVSVVQGVFSNNGRLSQDPYDLPKNSHIPCHYDLLPVRDSSSSPKQEDSGGSSSNSSSSSE
"
     misc_feature    363..2933
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q96KG7.1);
                     Region: Necessary for interaction with AP2M1,
                     self-assembly and formation of the irregular, mosaic-like
                     adhesion pattern"
     sig_peptide     363..437
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="COORDINATES: ab initio prediction:SignalP:4.0"
     mat_peptide     438..3782
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /product="Multiple epidermal growth factor-like domains
                     protein 10"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q96KG7.1)"
     misc_feature    450..668
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /note="EMI domain; Region: EMI; pfam07546"
                     /db_xref="CDD:148902"
     misc_feature    1203..1340
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /note="Laminin EGF-like (Domains III and V); Region:
                     Laminin_EGF; pfam00053"
                     /db_xref="CDD:200961"
     misc_feature    2934..2996
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q96KG7.1);
                     transmembrane region"
     misc_feature    3195..3782
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q96KG7.1);
                     Region: Necessary for formation of large intracellular
                     vacuoles"
     variation       412
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145733370"
     variation       452
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140458094"
     exon            479..580
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       482
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372038844"
     variation       533
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199718339"
     variation       536
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:12654455"
     variation       572
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369231278"
     variation       573
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:387907074"
     exon            581..681
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       585
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:146566192"
     variation       586
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:375736900"
     variation       613
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:370713978"
     variation       621
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:41298304"
     variation       629
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:368073107"
     variation       635
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:371481978"
     variation       665
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:77203884"
     variation       666
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200703478"
     variation       681
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200163743"
     exon            682..774
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       719
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376815672"
     variation       727
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375276332"
     exon            775..1021
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       776
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201114483"
     variation       779
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148349018"
     variation       807
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:201213540"
     variation       814
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:78069165"
     variation       844
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:57852581"
     variation       851
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:34649270"
     variation       874
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:201824269"
     variation       884
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201076330"
     variation       892
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373950666"
     variation       900
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142679354"
     variation       902
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:202145456"
     variation       904
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:377547826"
     variation       945
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368902561"
     variation       950
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:3812055"
     variation       958
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373163952"
     variation       971
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:113794264"
     variation       978
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:3812054"
     variation       993
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200236385"
     variation       994
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377520032"
     variation       1010
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144079313"
     variation       1014
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148663427"
     exon            1022..1142
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       1031
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:142221815"
     variation       1050
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372908552"
     variation       1087
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143420880"
     variation       1106
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:190469012"
     variation       1107
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370717384"
     exon            1143..1279
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       1169
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146742773"
     variation       1170
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201393832"
     variation       1226
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139531628"
     variation       1239
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144187055"
     variation       1252
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373114966"
     variation       1278
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371078929"
     exon            1280..1492
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       1280
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200870082"
     variation       1297
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199702225"
     variation       1313
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145870973"
     variation       1338
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:387907073"
     variation       1346
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:35550094"
     variation       1347
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148583278"
     variation       1364
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142947482"
     variation       1365
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:199600155"
     variation       1370
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145815113"
     variation       1373
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148970564"
     variation       1403
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:138524411"
     variation       1406
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:370219469"
     variation       1408
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:78847357"
     variation       1412
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201804815"
     variation       1417
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373605999"
     variation       1420
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146940427"
     variation       1433
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368784716"
     variation       1461
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377470998"
     variation       1462
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371522377"
     variation       1476
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:31483"
     variation       1488
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:151083652"
     exon            1493..1667
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       1503
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373994791"
     variation       1528
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141706024"
     variation       1531
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367855324"
     variation       1539
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150523119"
     variation       1553
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370883172"
     variation       1554
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:200174116"
     variation       1586
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139574266"
     variation       1621
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149288547"
     variation       1625
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146279465"
     variation       1640
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139438683"
     variation       1643
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370326593"
     exon            1668..1788
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       1726
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144145310"
     variation       1736
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:75552978"
     variation       1737
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:79671291"
     variation       1767
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373990545"
     exon            1789..1952
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       1796
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200050342"
     variation       1797
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372163689"
     variation       1822
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376778102"
     variation       1831
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202106748"
     variation       1862
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146075981"
     variation       1866
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:192423693"
     variation       1870
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148705070"
     variation       1871
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142355199"
     variation       1876
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199699950"
     variation       1885
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:184606767"
     variation       1895
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:151266058"
     variation       1914
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375925916"
     variation       1925
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372040705"
     variation       1926
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140563851"
     variation       1927
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:369959948"
     exon            1953..2055
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       1955
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375928516"
     variation       1960
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:150043761"
     variation       1964
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:114704569"
     variation       1984
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:142664089"
     variation       1988
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146902993"
     variation       2013
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:137909140"
     variation       2034
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374111304"
     variation       2035
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:182243856"
     variation       2044
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376978969"
     exon            2056..2202
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       2071
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368340848"
     variation       2073
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149021647"
     variation       2088
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143087353"
     variation       2089
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:201832505"
     variation       2112
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:148212621"
     variation       2130
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141190921"
     variation       2147
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:11950427"
     variation       2172
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:202135671"
     variation       2174
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375308597"
     variation       2176
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:138022464"
     variation       2201
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199930517"
     exon            2203..2337
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       2238
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:375356838"
     variation       2268
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201512679"
     variation       2288
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142667981"
     variation       2321
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146017981"
     exon            2338..2466
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       2351
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:372838715"
     variation       2369
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371031733"
     variation       2371
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375480261"
     variation       2383
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139700339"
     variation       2396
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:117124929"
     variation       2397
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199728470"
     variation       2436
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:144668169"
     variation       2438
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:115309591"
     variation       2450
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367788361"
     variation       2466
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:145440199"
     exon            2467..2595
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       2506
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:147731088"
     variation       2507
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200994008"
     variation       2512
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:116135607"
     variation       2519
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374544972"
     variation       2538
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139884665"
     variation       2561
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:35591368"
     variation       2563
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200026364"
     variation       2564
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369586831"
     exon            2596..2724
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       2627
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202151825"
     variation       2632
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367850011"
     variation       2651
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:151316424"
     variation       2663
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:387907071"
     variation       2664
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373093349"
     variation       2682
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:387907072"
     variation       2691
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377728219"
     variation       2700
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371145876"
     exon            2725..2853
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       2735
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:207466395"
     variation       2749..2750
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace=""
                     /replace="aaac"
                     /db_xref="dbSNP:141122304"
     variation       2758
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200317249"
     variation       2804
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370850456"
     variation       2825
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139929890"
     variation       2839
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150095036"
     exon            2854..3090
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       2893
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:138372925"
     STS             2935..3055
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /standard_name="MEGF10"
                     /db_xref="UniSTS:504913"
     variation       2945
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:138233141"
     variation       2948
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373601742"
     variation       2949
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148862988"
     variation       3016
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:116500162"
     variation       3036
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:367670148"
     variation       3052
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:13183625"
     variation       3063
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:375791814"
     variation       3066
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:138034219"
     variation       3080
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:41298310"
     exon            3091..3218
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       3095
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:200598050"
     variation       3113
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368185850"
     variation       3119
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:36061366"
     variation       3124
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:79861077"
     variation       3161
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146038027"
     variation       3210
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:148280932"
     exon            3219..3342
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       3243
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:141335036"
     variation       3254
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376690442"
     variation       3305
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371253627"
     variation       3323
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373066612"
     variation       3335
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375982019"
     exon            3343..3387
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       3365
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:35159176"
     exon            3388..3594
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       3448
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139251235"
     variation       3521
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143914256"
     variation       3524
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:17164938"
     variation       3532
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374156507"
     variation       3542
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144450528"
     variation       3545
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:368262600"
     variation       3546
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:75098905"
     variation       3551
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:56157640"
     variation       3558
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:200848884"
     variation       3577
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:17164935"
     variation       3578
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:75783175"
     variation       3591
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376652467"
     exon            3595..7689
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       3603
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:202070491"
     variation       3640
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:187800437"
     variation       3650
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:142969706"
     variation       3684
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:199899433"
     variation       3711
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376320089"
     variation       3716
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372767788"
     variation       3749
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:3812052"
     variation       3783
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:61738064"
     variation       3789
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:73783802"
     variation       3798
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372938701"
     variation       3808
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:377637251"
     variation       3837
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:182533165"
     variation       3859
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:186771376"
     variation       3878
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:192406612"
     variation       3883
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184598211"
     variation       3914
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371976049"
     variation       3949
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:187806833"
     variation       3977
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:151022976"
     variation       3994
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:10793809"
     variation       4082
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:192817098"
     variation       4142
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:78940206"
     variation       4156
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:185288474"
     variation       4211
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:189552285"
     variation       4222
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:181544163"
     variation       4232
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:183710966"
     variation       4236
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:188184559"
     variation       4266
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:75952196"
     variation       4319
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:75370992"
     variation       4386
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146027479"
     variation       4410
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:72790451"
     variation       4500..4503
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace=""
                     /replace="caga"
                     /db_xref="dbSNP:3841138"
     variation       4502..4505
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace=""
                     /replace="tgtt"
                     /db_xref="dbSNP:142781428"
     variation       4504..4507
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace=""
                     /replace="tttg"
                     /db_xref="dbSNP:376504887"
     variation       4617
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:180938359"
     variation       4636..4639
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace=""
                     /replace="gaca"
                     /db_xref="dbSNP:371105724"
     variation       4678
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375609485"
     variation       4700
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138844061"
     variation       4706
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141305722"
     variation       4718
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:17164927"
     variation       4742
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:114897100"
     variation       4790
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:76850984"
     variation       4813
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:186303123"
     variation       4837
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:192309131"
     variation       4882
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:137962522"
     variation       4935
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:75528418"
     STS             4948..5073
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /standard_name="WI-13521"
                     /db_xref="UniSTS:62957"
     variation       5031
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:17164925"
     variation       5081
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:55857193"
     variation       5097
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:76555555"
     variation       5172
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143870753"
     variation       5195
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:11745840"
     variation       5288
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:181716487"
     variation       5307
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:74560067"
     variation       5369
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:187137999"
     variation       5381
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:371809218"
     variation       5399
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143044754"
     variation       5470
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:17763722"
     variation       5595
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:17685202"
     variation       5691
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140140161"
     variation       5787
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:191111952"
     variation       5808
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:372595076"
     variation       5851
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112337118"
     variation       5883
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:79556392"
     variation       5898
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:183376722"
     variation       5899
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:77171194"
     variation       5934
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:3756721"
     variation       6006..6007
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:34268883"
     variation       6021
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:3756722"
     variation       6025
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:77136524"
     variation       6270
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:141495648"
     variation       6304
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:187089787"
     variation       6334
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:75434042"
     variation       6379
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:189578341"
     variation       6668
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2115242"
     variation       6696
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:182225709"
     variation       6751
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:2840011"
     variation       6754..6755
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace=""
                     /replace="at"
                     /db_xref="dbSNP:374521779"
     variation       6876
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:187542520"
     variation       6916
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:193298014"
     variation       6924
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:185113856"
     variation       6960
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:76059053"
     variation       6969
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150862535"
     variation       6976
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:188780004"
     variation       7010
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:78458032"
     variation       7139
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369417628"
     variation       7307..7308
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace=""
                     /replace="ca"
                     /db_xref="dbSNP:35236935"
     variation       7351
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:139305981"
     variation       7360
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:2898043"
     variation       7400
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149991413"
     variation       7496
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147664195"
     variation       7522
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:140678815"
     variation       7556..7558
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace=""
                     /replace="aac"
                     /db_xref="dbSNP:369828369"
     variation       7588
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:192951344"
     polyA_signal    7669..7674
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
     polyA_site      7689
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
ORIGIN      
acccgcccccaccccctccagcatctcgggccagacagagaaaaccttgttcaagtttgcagcaagtactttcccggtgcgcaaaactgggcgactgggaacgcgttgagacgttcctctttcccgcttctccacctttacgcctgaaagaagactcccaaagattgctttcttctgggacgctgcttggacgctaaccgcgttgattggaacagattttgtgtcttggctggctttgggtgaagaccggggagaaaaggttgcgctgcgattctcaagatctctggacctggattatcattgcaaatccattaaagaaggagaagcaagcggatttcagagaggttgttcttcagaaaaaaatggttatttctttgaactcatgcctgagctttatttgtttattgttatgccactggattgggacagcatcacctctgaatcttgaagaccctaatgtgtgtagccactgggaaagctactcagtgactgtgcaagagtcatacccacatccctttgatcaaatttactacacgagctgcactgacattctaaactggtttaaatgcacgcggcacagagtcagctatcggacagcctatcgacatggggagaagactatgtataggcgcaagtctcagtgttgtcctggattttatgaaagcggggaaatgtgtgtcccccactgtgctgataaatgtgtccatggtcgctgtattgctccaaacacctgtcagtgtgagcctggctggggagggaccaactgctccagtgcctgcgatggtgatcactggggtccccactgcaccagccggtgccagtgcaaaaatggggctctgtgcaaccccatcaccggggcttgccactgtgctgcgggcttccggggctggcgctgcgaggaccgctgtgagcagggcacctatggtaacgactgtcatcagagatgccagtgccagaatggagccacctgcgaccacgtcacgggggaatgccgctgcccaccaggatacaccggagccttctgtgaggatctttgtcctcctggtaaacatggtccacagtgtgagcagagatgcccttgtcaaaatggaggagtgtgtcatcacgtcactggagaatgctcttgcccttctggctggatgggcacagtgtgtggtcagccttgccccgagggtcgctttggaaagaactgttcccaagaatgccagtgccataatggagggacgtgtgatgctgccacaggccaatgtcattgcagtccaggatacacaggggaacggtgccaggatgagtgtcctgttgggacctatggcgttctctgtgctgagacctgccagtgtgtcaacggagggaagtgttaccacgtgagcggcgcatgcctctgtgaagcaggctttgctggcgagcgctgcgaagcacgcctgtgtcctgaggggctctacggcatcaaatgtgacaaacggtgtccctgccacctggaaaacactcatagctgtcaccccatgtctggagagtgtgcctgcaagccgggctggtcaggactctactgtaatgagacatgttctcctggattctacggggaagcttgccagcagatctgcagctgccaaaatggggcagactgtgacagtgtgactggaaagtgcacctgtgccccaggattcaaaggaattgactgctctaccccatgccctctgggaacctatgggataaactgttcctctcgctgtggctgtaaaaatgatgcagtctgctctcctgtggacgggtcttgtacttgcaaggcaggctggcacggggtggactgctccatcagatgtcccagtggcacatggggctttggctgtaacttaacatgccagtgcctcaacgggggagcctgcaacaccctggacgggacctgcacgtgtgcacctggatggcgcggggagaaatgcgaacttccctgccaggatggcacgtacgggctgaactgtgctgagcgctgcgactgcagccacgcagatggctgccaccctaccacgggccattgccgctgcctccccggatggtcaggtgtccactgtgacagcgtgtgtgctgagggacgctggggccccaactgctccctgccctgctactgtaaaaatggggcttcatgctcccctgatgatggcatctgcgagtgtgcaccaggcttccgaggcaccacttgtcagaggatctgctcccctggtttttatgggcatcgctgcagccagacatgcccacagtgcgttcacagcagcgggccctgccaccacatcaccggcctgtgtgactgcttgcctggcttcacaggcgccctctgcaatgaagtgtgtcccagtggcagatttgggaaaaactgtgcaggaatttgtacctgcaccaacaacggaacctgtaaccccattgacagatcttgtcagtgttaccccggttggattggcagtgactgctctcaaccatgtccacctgcccactggggcccaaactgcatccacacgtgcaactgccataatggagctttctgcagcgcctacgatggggaatgtaaatgcactcctggctggacagggctctactgcactcagagatgtcctctagggttttatggaaaagattgtgcactgatatgccaatgtcaaaacggagctgactgcgaccacatttctgggcagtgtacttgccgcactggattcatgggacggcactgtgagcagaagtgcccttcaggaacatatggctatggctgtcgccagatatgtgattgtctgaacaactccacctgcgaccacatcactgggacctgttactgcagccccggatggaagggagcgagatgtgatcaagctggtgttatcatagttggaaatctgaacagcttaagccgaaccagtactgctctccctgctgattcctaccagatcggggccattgcaggcatcatcattcttgtcctagttgttctcttcctactggcattgttcattatttatagacacaagcagaagggaaaggaatcaagcatgccagcagttacctacacccctgctatgagggtcgtcaatgcagattataccatttcaggaacccttcctcacagcaatggtggaaacgctaatagccactacttcaccaatcccagttaccacacgctcacccagtgtgccacatcccctcacgtcaacaacagggacaggatgactgtcacgaagtcaaaaaacaatcaactgtttgtgaatcttaaaaatgtgaaccctgggaagagaggccctgtgggggactgcactgggacattgccggctgactggaaacatggcggctacctcaacgagctcggtgcttttggacttgacagaagctatatgggaaaatccttaaaagacctgggaaagaattctgaatataattcaagtaactgctccctaagcagttctgagaacccatatgccactattaaagacccacctgtacttatcccgaaaagctcagagtgtggttatgtggagatgaaatcgccggcacgaagagattccccatatgcagagatcaataactcaacttcagccaacaggaatgtctatgaagttgaacctacagtgagtgttgtccaaggagtattcagcaataatgggcgtctctcccaggatccatatgacctcccaaagaacagtcacatcccttgtcattatgacctgctgccagtccgagacagttcatcctcccctaagcaagaggacagtggtggtagcagcagcaacagcagcagcagcagtgaatgacaccaaaggaccgcttggtagccactggaaccctttccagaactgctgtttggttcttctccatcctcaattttgccactttcatgtgaatgttagtcaattcggtgggcaatttttggacatgaaccagaaagctgaaagctgaggctgacacggactgtaggtgctttttgttcaggtggattcgaaggagttagagatgtgatttcccattgctgttagttttagaactatacccgtgaagcatgacttattgtaagatgttggctgaaagcatgaacttgcagaactccctcggagacgcaggttgcagtggacattgggattgttgcttgaaaaattaaaatttgaatattttctctctcatttgcatcatacagctctacctaggattgtacagtttaccataaaatttacttcatgaaagtgggaatcactgaacatgtagaagacaaggaacatattgttaactcctgattcttaactttattcaactggactcagaattgtagggataatatgaatgcaggaggaaacattctgtcaggcggtatgactggacagactttgaatatactctaaaagtggacagaaaatttacgaaaatcttagattttgtttagaatgagaaaatatacaattagaattattttagaaatagtaggaagtattgcagaagtcaatacacaaatgtgccaggcagaggtggttttctctgtttgactctcaaccaacttcagatctatgacattattctgatcactggctccatcatacatattcaccacttgagattcataacatatcaatagttatttcataaatatagaaatgaaataattttatttttgacagactggatggaatgagtgtgtaatgattgataaaggttgtaaattttaaatgcaagatgacgcttacgttctgtaaaccattagtaatacatgctgtaatatagaattagtggaacattttgattaatctttccctagaagtgactgaaatatttttgtgcatatttgagaaagggaactttccttttattaattgtcaatttagagaaactatgcttaagctggtcttttgcattgctaatgtgacatgtacccaacttttcattaatttgtatttccatttttaaattgcatattctatgttttgtagtgtttggattgttaatgaaaaaatattatatgttcgttattccttgtattattgccacttatcttttgcttgataaaaatgcgttgttcttttttcttttggagggacaagatgaaaatatataatttgaattgattaaaattggtcgttactaaaatagtatagtaaccacaagtgattggcttataaatgaagtagaaatgctttttaatattccaaaatagagttccttttgatctgttggtgctgagccttggttaaaccagggagaaggggagcagaaaggaaacgttgttactgatgagtaccacagactcatcttaaaaaaaactctcattatggtgatcatagaattgaccatccaaactgggacactcttgagagtaaatggagggcattattaataattatcttgtaatgaacttaaatctggactgttccaggcaaaccagacttatcttgcaatatgagaatgctgacacaatgcaggaaagccagtttcccttttgttgatctacttgaccaagcaaaggggctgaaaaactgaataaggaaacaactttataagagaaacagtggtcttcaatcttttaaagacatgaaatcctatatggcattctgtctcagtgagtcagttaacaaatacgtatgtgcaacccttctgctagtagtgcacataagtgattatccctgccaggtatcgagttggaatatccagttatttcatgtcacacatcggcacgtatgatggtggtttggtcagatggataatacagcagacacacttagaacactcactgcactggtggctgttcattttgaggaactccaaagtcaattcaaggaaataaggaatgacctggaacaggccttagaaacaattgatttattccaatagttaaccactggctggctcccaactctaggtgataggcatctaattgagacatgtgtgagtcaatagccatcggggtcctttttggtgagaagaaataagacattttctcccttttaaagatcatctcttcagagctgcatggtaaatttgaatttccccattgttctctagagctaggtcaaaaaaacaactgtttcttttcttattccactattaataaattgaaagcttgctgtacaaaggcaacagcaacttaaaaaagaaaatctggacaatagatgtggactccaaggggccactgccatcccttcctgtgtgctctttttgacaagtaaatcactccagttagctgatgtcctgaaatgacatttgtacctgaggcaattcttattagagcttactcaggacttttcaaacatcaggacacacatagcaatttggatgttgtaaaactacgtgttacatttggagaggtcttgttgagaaggcaaaattttctaaatattttgatatcaatttgggtaaagaaaggaatacttttgttagaatgagaattaaagagaaaacaaaagaatcttggcaaaattttccctctgaaattacaaactttaggaacttttccagatgtatcgaatttaatttgacattgatgtcactcttcataccaagtgaatctattctcatgaactttgaacccatgttaattttggaccctataactaatttcctttctgtatcccatggtggtcaaagcagtaaaggagtttagagatacttagcaaatgccattcatatagtattgttagccaaactattattccttccttagaagttgatgtatcagaaaatttataagttatttgtatttatatataagtacatcagaacttgcccacatgataactcatgtttgctttaataaggaaaatatgttatttgaggttaattatatgatagtgaggaacattttacaattatttacagtgtttgacattaattgctgtcctatgatacagtagtaatgttaacagagagtttaatatgtttagcattatctttatggaatttatattcaccaatttcaggaaaaccaaccatagaactttataataggacagttataacctgactgaaccaaatccatcagcataatgactgtgtgttctgagaaatgcaaacaactttatgaaagtgtggtcatcttgacccccaaagagccacagtagctgtcaattattgagatttttaaatggtaaatattgcaaaagttaaacaagggtaccacaatatcatttataattgatgtcaatattagtagtccactttatgcttaaaataaaatcataaaaaatcaagttttaaggttatattttttaaaataatgaattttctatctctaggcaacatgtctttattattcaagctgaatgtttaagagagattttggtcttaaaggcttcacatcatgaaagtgtacatgcatatgcaagtgtgaattacgtggtatggatgtttgcttgtttattaactaaagatgtacagcaaactgcccgtttagagtcctgttaatattgatgtcctaacactgggtctgcttatgctagttcagtatttggtctaggcttcattttgatatgactgaattgcaatctatatttttaaaaagaaaaatcaaaatacattagggtttacttggttgtggcaaacaaacaaaaaatgctttcagtgttgaaatatctctattttccaaagatgataaactttcatcgttcttagcctacattgtcatttatatcaccaaatgagtttatagattaatgcaataaactttctaataaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:84466 -> Biological process: GO:0014719 [satellite cell activation] evidence: ISS
            GeneID:84466 -> Biological process: GO:0014816 [satellite cell differentiation] evidence: IMP
            GeneID:84466 -> Biological process: GO:0014841 [satellite cell proliferation] evidence: ISS
            GeneID:84466 -> Biological process: GO:0034109 [homotypic cell-cell adhesion] evidence: IDA
            GeneID:84466 -> Biological process: GO:0043654 [recognition of apoptotic cell] evidence: IEA
            GeneID:84466 -> Biological process: GO:0048641 [regulation of skeletal muscle tissue development] evidence: IMP
            GeneID:84466 -> Biological process: GO:0051147 [regulation of muscle cell differentiation] evidence: IMP
            GeneID:84466 -> Biological process: GO:0055001 [muscle cell development] evidence: IMP
            GeneID:84466 -> Cellular component: GO:0001891 [phagocytic cup] evidence: IEA
            GeneID:84466 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA
            GeneID:84466 -> Cellular component: GO:0016323 [basolateral plasma membrane] evidence: IEA
            GeneID:84466 -> Cellular component: GO:0042995 [cell projection] evidence: IEA

by @meso_cacase at DBCLS
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