GGRNA Home | Help | Advanced search

2024-03-29 02:32:36, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001256545            7638 bp    mRNA    linear   PRI 29-JUN-2013
DEFINITION  Homo sapiens multiple EGF-like-domains 10 (MEGF10), transcript
            variant 2, mRNA.
ACCESSION   NM_001256545
VERSION     NM_001256545.1  GI:375065829
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 7638)
  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 7638)
  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 7638)
  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 7638)
  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 7638)
  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 7638)
  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 7638)
  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 7638)
  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 7638)
  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 7638)
  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, CR749437.1,
            AC008682.6, DA738723.1 and AC010424.9.
            
            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 (2) differs in the 5' UTR compared
            to variant 1. 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 :: CR749437.1 [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
            1-67                DA240513.1         1-67
            68-1424             CR749437.1         2-1358
            1425-1425           AC008682.6         91165-91165         c
            1426-1938           CR749437.1         1360-1872
            1939-2099           DA738723.1         214-374
            2100-3697           CR749437.1         2034-3631
            3698-7638           AC010424.9         26200-30140
FEATURES             Location/Qualifiers
     source          1..7638
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="5"
                     /map="5q33"
     gene            1..7638
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /note="multiple EGF-like-domains 10"
                     /db_xref="GeneID:84466"
                     /db_xref="HGNC:29634"
                     /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..427
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       305
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:4620069"
     CDS             312..3734
                     /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_001243474.1"
                     /db_xref="GI:375065830"
                     /db_xref="CCDS:CCDS4142.1"
                     /db_xref="GeneID:84466"
                     /db_xref="HGNC:29634"
                     /db_xref="MIM:612453"
                     /translation="
MVISLNSCLSFICLLLCHWIGTASPLNLEDPNVCSHWESYSVTVQESYPHPFDQIYYTSCTDILNWFKCTRHRVSYRTAYRHGEKTMYRRKSQCCPGFYESGEMCVPHCADKCVHGRCIAPNTCQCEPGWGGTNCSSACDGDHWGPHCTSRCQCKNGALCNPITGACHCAAGFRGWRCEDRCEQGTYGNDCHQRCQCQNGATCDHVTGECRCPPGYTGAFCEDLCPPGKHGPQCEQRCPCQNGGVCHHVTGECSCPSGWMGTVCGQPCPEGRFGKNCSQECQCHNGGTCDAATGQCHCSPGYTGERCQDECPVGTYGVLCAETCQCVNGGKCYHVSGACLCEAGFAGERCEARLCPEGLYGIKCDKRCPCHLENTHSCHPMSGECACKPGWSGLYCNETCSPGFYGEACQQICSCQNGADCDSVTGKCTCAPGFKGIDCSTPCPLGTYGINCSSRCGCKNDAVCSPVDGSCTCKAGWHGVDCSIRCPSGTWGFGCNLTCQCLNGGACNTLDGTCTCAPGWRGEKCELPCQDGTYGLNCAERCDCSHADGCHPTTGHCRCLPGWSGVHCDSVCAEGRWGPNCSLPCYCKNGASCSPDDGICECAPGFRGTTCQRICSPGFYGHRCSQTCPQCVHSSGPCHHITGLCDCLPGFTGALCNEVCPSGRFGKNCAGICTCTNNGTCNPIDRSCQCYPGWIGSDCSQPCPPAHWGPNCIHTCNCHNGAFCSAYDGECKCTPGWTGLYCTQRCPLGFYGKDCALICQCQNGADCDHISGQCTCRTGFMGRHCEQKCPSGTYGYGCRQICDCLNNSTCDHITGTCYCSPGWKGARCDQAGVIIVGNLNSLSRTSTALPADSYQIGAIAGIIILVLVVLFLLALFIIYRHKQKGKESSMPAVTYTPAMRVVNADYTISGTLPHSNGGNANSHYFTNPSYHTLTQCATSPHVNNRDRMTVTKSKNNQLFVNLKNVNPGKRGPVGDCTGTLPADWKHGGYLNELGAFGLDRSYMGKSLKDLGKNSEYNSSNCSLSSSENPYATIKDPPVLIPKSSECGYVEMKSPARRDSPYAEINNSTSANRNVYEVEPTVSVVQGVFSNNGRLSQDPYDLPKNSHIPCHYDLLPVRDSSSSPKQEDSGGSSSNSSSSSE
"
     misc_feature    312..2882
                     /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     312..386
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="COORDINATES: ab initio prediction:SignalP:4.0"
     mat_peptide     387..3731
                     /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    399..617
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /note="EMI domain; Region: EMI; pfam07546"
                     /db_xref="CDD:148902"
     misc_feature    1152..1289
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /note="Laminin EGF-like (Domains III and V); Region:
                     Laminin_EGF; pfam00053"
                     /db_xref="CDD:200961"
     misc_feature    2883..2945
                     /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    3144..3731
                     /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       361
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145733370"
     variation       401
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140458094"
     exon            428..529
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       431
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372038844"
     variation       482
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199718339"
     variation       485
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:12654455"
     variation       521
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369231278"
     variation       522
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:387907074"
     exon            530..630
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       534
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:146566192"
     variation       535
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:375736900"
     variation       562
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:370713978"
     variation       570
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:41298304"
     variation       578
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:368073107"
     variation       584
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:371481978"
     variation       614
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:77203884"
     variation       615
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200703478"
     variation       630
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200163743"
     exon            631..723
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       668
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376815672"
     variation       676
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375276332"
     exon            724..970
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       725
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201114483"
     variation       728
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148349018"
     variation       756
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:201213540"
     variation       763
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:78069165"
     variation       793
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:57852581"
     variation       800
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:34649270"
     variation       823
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:201824269"
     variation       833
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201076330"
     variation       841
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373950666"
     variation       849
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142679354"
     variation       851
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:202145456"
     variation       853
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:377547826"
     variation       894
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368902561"
     variation       899
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:3812055"
     variation       907
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373163952"
     variation       920
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:113794264"
     variation       927
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:3812054"
     variation       942
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200236385"
     variation       943
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377520032"
     variation       959
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144079313"
     variation       963
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148663427"
     exon            971..1091
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       980
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:142221815"
     variation       999
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372908552"
     variation       1036
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143420880"
     variation       1055
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:190469012"
     variation       1056
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370717384"
     exon            1092..1228
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       1118
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146742773"
     variation       1119
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201393832"
     variation       1175
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139531628"
     variation       1188
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144187055"
     variation       1201
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373114966"
     variation       1227
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371078929"
     exon            1229..1441
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       1229
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200870082"
     variation       1246
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199702225"
     variation       1262
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145870973"
     variation       1287
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:387907073"
     variation       1295
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:35550094"
     variation       1296
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148583278"
     variation       1313
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142947482"
     variation       1314
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:199600155"
     variation       1319
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145815113"
     variation       1322
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148970564"
     variation       1352
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:138524411"
     variation       1355
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:370219469"
     variation       1357
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:78847357"
     variation       1361
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201804815"
     variation       1366
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373605999"
     variation       1369
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146940427"
     variation       1382
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368784716"
     variation       1410
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377470998"
     variation       1411
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371522377"
     variation       1425
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:31483"
     variation       1437
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:151083652"
     exon            1442..1616
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       1452
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373994791"
     variation       1477
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141706024"
     variation       1480
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367855324"
     variation       1488
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150523119"
     variation       1502
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370883172"
     variation       1503
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:200174116"
     variation       1535
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139574266"
     variation       1570
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149288547"
     variation       1574
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146279465"
     variation       1589
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139438683"
     variation       1592
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370326593"
     exon            1617..1737
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       1675
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144145310"
     variation       1685
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:75552978"
     variation       1686
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:79671291"
     variation       1716
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373990545"
     exon            1738..1901
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       1745
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200050342"
     variation       1746
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372163689"
     variation       1771
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376778102"
     variation       1780
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202106748"
     variation       1811
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146075981"
     variation       1815
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:192423693"
     variation       1819
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148705070"
     variation       1820
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142355199"
     variation       1825
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199699950"
     variation       1834
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:184606767"
     variation       1844
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:151266058"
     variation       1863
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375925916"
     variation       1874
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372040705"
     variation       1875
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140563851"
     variation       1876
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:369959948"
     exon            1902..2004
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       1904
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375928516"
     variation       1909
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:150043761"
     variation       1913
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:114704569"
     variation       1933
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:142664089"
     variation       1937
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146902993"
     variation       1962
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:137909140"
     variation       1983
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374111304"
     variation       1984
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:182243856"
     variation       1993
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376978969"
     exon            2005..2151
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       2020
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368340848"
     variation       2022
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149021647"
     variation       2037
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143087353"
     variation       2038
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:201832505"
     variation       2061
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:148212621"
     variation       2079
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141190921"
     variation       2096
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:11950427"
     variation       2121
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:202135671"
     variation       2123
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375308597"
     variation       2125
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:138022464"
     variation       2150
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199930517"
     exon            2152..2286
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       2187
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:375356838"
     variation       2217
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201512679"
     variation       2237
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142667981"
     variation       2270
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146017981"
     exon            2287..2415
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       2300
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:372838715"
     variation       2318
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371031733"
     variation       2320
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375480261"
     variation       2332
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139700339"
     variation       2345
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:117124929"
     variation       2346
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199728470"
     variation       2385
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:144668169"
     variation       2387
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:115309591"
     variation       2399
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367788361"
     variation       2415
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:145440199"
     exon            2416..2544
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       2455
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:147731088"
     variation       2456
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200994008"
     variation       2461
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:116135607"
     variation       2468
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374544972"
     variation       2487
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139884665"
     variation       2510
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:35591368"
     variation       2512
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200026364"
     variation       2513
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369586831"
     exon            2545..2673
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       2576
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202151825"
     variation       2581
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367850011"
     variation       2600
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:151316424"
     variation       2612
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:387907071"
     variation       2613
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373093349"
     variation       2631
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:387907072"
     variation       2640
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377728219"
     variation       2649
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371145876"
     exon            2674..2802
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       2684
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:207466395"
     variation       2698..2699
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace=""
                     /replace="aaac"
                     /db_xref="dbSNP:141122304"
     variation       2707
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200317249"
     variation       2753
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370850456"
     variation       2774
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139929890"
     variation       2788
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150095036"
     exon            2803..3039
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       2842
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:138372925"
     STS             2884..3004
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /standard_name="MEGF10"
                     /db_xref="UniSTS:504913"
     variation       2894
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:138233141"
     variation       2897
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373601742"
     variation       2898
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148862988"
     variation       2965
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:116500162"
     variation       2985
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:367670148"
     variation       3001
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:13183625"
     variation       3012
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:375791814"
     variation       3015
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:138034219"
     variation       3029
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:41298310"
     exon            3040..3167
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       3044
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:200598050"
     variation       3062
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368185850"
     variation       3068
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:36061366"
     variation       3073
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:79861077"
     variation       3110
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146038027"
     variation       3159
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:148280932"
     exon            3168..3291
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       3192
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:141335036"
     variation       3203
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376690442"
     variation       3254
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371253627"
     variation       3272
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373066612"
     variation       3284
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375982019"
     exon            3292..3336
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       3314
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:35159176"
     exon            3337..3543
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       3397
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139251235"
     variation       3470
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143914256"
     variation       3473
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:17164938"
     variation       3481
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374156507"
     variation       3491
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144450528"
     variation       3494
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:368262600"
     variation       3495
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:75098905"
     variation       3500
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:56157640"
     variation       3507
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:200848884"
     variation       3526
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:17164935"
     variation       3527
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:75783175"
     variation       3540
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376652467"
     exon            3544..7638
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /inference="alignment:Splign:1.39.8"
     variation       3552
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:202070491"
     variation       3589
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:187800437"
     variation       3599
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:142969706"
     variation       3633
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:199899433"
     variation       3660
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376320089"
     variation       3665
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372767788"
     variation       3698
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:3812052"
     variation       3732
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:61738064"
     variation       3738
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:73783802"
     variation       3747
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372938701"
     variation       3757
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:377637251"
     variation       3786
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:182533165"
     variation       3808
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:186771376"
     variation       3827
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:192406612"
     variation       3832
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184598211"
     variation       3863
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371976049"
     variation       3898
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:187806833"
     variation       3926
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:151022976"
     variation       3943
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:10793809"
     variation       4031
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:192817098"
     variation       4091
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:78940206"
     variation       4105
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:185288474"
     variation       4160
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:189552285"
     variation       4171
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:181544163"
     variation       4181
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:183710966"
     variation       4185
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:188184559"
     variation       4215
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:75952196"
     variation       4268
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:75370992"
     variation       4335
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146027479"
     variation       4359
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:72790451"
     variation       4449..4452
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace=""
                     /replace="caga"
                     /db_xref="dbSNP:3841138"
     variation       4451..4454
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace=""
                     /replace="tgtt"
                     /db_xref="dbSNP:142781428"
     variation       4453..4456
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace=""
                     /replace="tttg"
                     /db_xref="dbSNP:376504887"
     variation       4566
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:180938359"
     variation       4585..4588
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace=""
                     /replace="gaca"
                     /db_xref="dbSNP:371105724"
     variation       4627
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375609485"
     variation       4649
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138844061"
     variation       4655
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141305722"
     variation       4667
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:17164927"
     variation       4691
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:114897100"
     variation       4739
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:76850984"
     variation       4762
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:186303123"
     variation       4786
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:192309131"
     variation       4831
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:137962522"
     variation       4884
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:75528418"
     STS             4897..5022
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /standard_name="WI-13521"
                     /db_xref="UniSTS:62957"
     variation       4980
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:17164925"
     variation       5030
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:55857193"
     variation       5046
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:76555555"
     variation       5121
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143870753"
     variation       5144
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:11745840"
     variation       5237
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:181716487"
     variation       5256
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:74560067"
     variation       5318
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:187137999"
     variation       5330
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:371809218"
     variation       5348
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143044754"
     variation       5419
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:17763722"
     variation       5544
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:17685202"
     variation       5640
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140140161"
     variation       5736
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:191111952"
     variation       5757
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:372595076"
     variation       5800
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112337118"
     variation       5832
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:79556392"
     variation       5847
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:183376722"
     variation       5848
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:77171194"
     variation       5883
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:3756721"
     variation       5955..5956
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:34268883"
     variation       5970
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:3756722"
     variation       5974
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:77136524"
     variation       6219
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:141495648"
     variation       6253
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:187089787"
     variation       6283
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:75434042"
     variation       6328
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:189578341"
     variation       6617
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2115242"
     variation       6645
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:182225709"
     variation       6700
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:2840011"
     variation       6703..6704
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace=""
                     /replace="at"
                     /db_xref="dbSNP:374521779"
     variation       6825
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:187542520"
     variation       6865
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:193298014"
     variation       6873
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:185113856"
     variation       6909
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:76059053"
     variation       6918
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150862535"
     variation       6925
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:188780004"
     variation       6959
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:78458032"
     variation       7088
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369417628"
     variation       7256..7257
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace=""
                     /replace="ca"
                     /db_xref="dbSNP:35236935"
     variation       7300
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:139305981"
     variation       7309
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:2898043"
     variation       7349
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149991413"
     variation       7445
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147664195"
     variation       7471
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:140678815"
     variation       7505..7507
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace=""
                     /replace="aac"
                     /db_xref="dbSNP:369828369"
     variation       7537
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:192951344"
     polyA_signal    7618..7623
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
     polyA_site      7638
                     /gene="MEGF10"
                     /gene_synonym="EMARDD"
ORIGIN      
acccgcccccaccccctccagcatctcgggccagacagagaaaaccttgttcaagtttgcagcaagtactttcccggtgcgcaaaactgggcgactgggaacgcgttgagacgttcctctttcccgcttctccacctttacgcctgaaagaagactcccaaagattgctttcttctgggacgctgcttggacgctaaccgcgttgattggaacagattttgtgtcttggctggctttgggtgaagaccggggagaaaaggttgcgctgcgattctcaagatctctggacctgggttgttcttcagaaaaaaatggttatttctttgaactcatgcctgagctttatttgtttattgttatgccactggattgggacagcatcacctctgaatcttgaagaccctaatgtgtgtagccactgggaaagctactcagtgactgtgcaagagtcatacccacatccctttgatcaaatttactacacgagctgcactgacattctaaactggtttaaatgcacgcggcacagagtcagctatcggacagcctatcgacatggggagaagactatgtataggcgcaagtctcagtgttgtcctggattttatgaaagcggggaaatgtgtgtcccccactgtgctgataaatgtgtccatggtcgctgtattgctccaaacacctgtcagtgtgagcctggctggggagggaccaactgctccagtgcctgcgatggtgatcactggggtccccactgcaccagccggtgccagtgcaaaaatggggctctgtgcaaccccatcaccggggcttgccactgtgctgcgggcttccggggctggcgctgcgaggaccgctgtgagcagggcacctatggtaacgactgtcatcagagatgccagtgccagaatggagccacctgcgaccacgtcacgggggaatgccgctgcccaccaggatacaccggagccttctgtgaggatctttgtcctcctggtaaacatggtccacagtgtgagcagagatgcccttgtcaaaatggaggagtgtgtcatcacgtcactggagaatgctcttgcccttctggctggatgggcacagtgtgtggtcagccttgccccgagggtcgctttggaaagaactgttcccaagaatgccagtgccataatggagggacgtgtgatgctgccacaggccaatgtcattgcagtccaggatacacaggggaacggtgccaggatgagtgtcctgttgggacctatggcgttctctgtgctgagacctgccagtgtgtcaacggagggaagtgttaccacgtgagcggcgcatgcctctgtgaagcaggctttgctggcgagcgctgcgaagcacgcctgtgtcctgaggggctctacggcatcaaatgtgacaaacggtgtccctgccacctggaaaacactcatagctgtcaccccatgtctggagagtgtgcctgcaagccgggctggtcaggactctactgtaatgagacatgttctcctggattctacggggaagcttgccagcagatctgcagctgccaaaatggggcagactgtgacagtgtgactggaaagtgcacctgtgccccaggattcaaaggaattgactgctctaccccatgccctctgggaacctatgggataaactgttcctctcgctgtggctgtaaaaatgatgcagtctgctctcctgtggacgggtcttgtacttgcaaggcaggctggcacggggtggactgctccatcagatgtcccagtggcacatggggctttggctgtaacttaacatgccagtgcctcaacgggggagcctgcaacaccctggacgggacctgcacgtgtgcacctggatggcgcggggagaaatgcgaacttccctgccaggatggcacgtacgggctgaactgtgctgagcgctgcgactgcagccacgcagatggctgccaccctaccacgggccattgccgctgcctccccggatggtcaggtgtccactgtgacagcgtgtgtgctgagggacgctggggccccaactgctccctgccctgctactgtaaaaatggggcttcatgctcccctgatgatggcatctgcgagtgtgcaccaggcttccgaggcaccacttgtcagaggatctgctcccctggtttttatgggcatcgctgcagccagacatgcccacagtgcgttcacagcagcgggccctgccaccacatcaccggcctgtgtgactgcttgcctggcttcacaggcgccctctgcaatgaagtgtgtcccagtggcagatttgggaaaaactgtgcaggaatttgtacctgcaccaacaacggaacctgtaaccccattgacagatcttgtcagtgttaccccggttggattggcagtgactgctctcaaccatgtccacctgcccactggggcccaaactgcatccacacgtgcaactgccataatggagctttctgcagcgcctacgatggggaatgtaaatgcactcctggctggacagggctctactgcactcagagatgtcctctagggttttatggaaaagattgtgcactgatatgccaatgtcaaaacggagctgactgcgaccacatttctgggcagtgtacttgccgcactggattcatgggacggcactgtgagcagaagtgcccttcaggaacatatggctatggctgtcgccagatatgtgattgtctgaacaactccacctgcgaccacatcactgggacctgttactgcagccccggatggaagggagcgagatgtgatcaagctggtgttatcatagttggaaatctgaacagcttaagccgaaccagtactgctctccctgctgattcctaccagatcggggccattgcaggcatcatcattcttgtcctagttgttctcttcctactggcattgttcattatttatagacacaagcagaagggaaaggaatcaagcatgccagcagttacctacacccctgctatgagggtcgtcaatgcagattataccatttcaggaacccttcctcacagcaatggtggaaacgctaatagccactacttcaccaatcccagttaccacacgctcacccagtgtgccacatcccctcacgtcaacaacagggacaggatgactgtcacgaagtcaaaaaacaatcaactgtttgtgaatcttaaaaatgtgaaccctgggaagagaggccctgtgggggactgcactgggacattgccggctgactggaaacatggcggctacctcaacgagctcggtgcttttggacttgacagaagctatatgggaaaatccttaaaagacctgggaaagaattctgaatataattcaagtaactgctccctaagcagttctgagaacccatatgccactattaaagacccacctgtacttatcccgaaaagctcagagtgtggttatgtggagatgaaatcgccggcacgaagagattccccatatgcagagatcaataactcaacttcagccaacaggaatgtctatgaagttgaacctacagtgagtgttgtccaaggagtattcagcaataatgggcgtctctcccaggatccatatgacctcccaaagaacagtcacatcccttgtcattatgacctgctgccagtccgagacagttcatcctcccctaagcaagaggacagtggtggtagcagcagcaacagcagcagcagcagtgaatgacaccaaaggaccgcttggtagccactggaaccctttccagaactgctgtttggttcttctccatcctcaattttgccactttcatgtgaatgttagtcaattcggtgggcaatttttggacatgaaccagaaagctgaaagctgaggctgacacggactgtaggtgctttttgttcaggtggattcgaaggagttagagatgtgatttcccattgctgttagttttagaactatacccgtgaagcatgacttattgtaagatgttggctgaaagcatgaacttgcagaactccctcggagacgcaggttgcagtggacattgggattgttgcttgaaaaattaaaatttgaatattttctctctcatttgcatcatacagctctacctaggattgtacagtttaccataaaatttacttcatgaaagtgggaatcactgaacatgtagaagacaaggaacatattgttaactcctgattcttaactttattcaactggactcagaattgtagggataatatgaatgcaggaggaaacattctgtcaggcggtatgactggacagactttgaatatactctaaaagtggacagaaaatttacgaaaatcttagattttgtttagaatgagaaaatatacaattagaattattttagaaatagtaggaagtattgcagaagtcaatacacaaatgtgccaggcagaggtggttttctctgtttgactctcaaccaacttcagatctatgacattattctgatcactggctccatcatacatattcaccacttgagattcataacatatcaatagttatttcataaatatagaaatgaaataattttatttttgacagactggatggaatgagtgtgtaatgattgataaaggttgtaaattttaaatgcaagatgacgcttacgttctgtaaaccattagtaatacatgctgtaatatagaattagtggaacattttgattaatctttccctagaagtgactgaaatatttttgtgcatatttgagaaagggaactttccttttattaattgtcaatttagagaaactatgcttaagctggtcttttgcattgctaatgtgacatgtacccaacttttcattaatttgtatttccatttttaaattgcatattctatgttttgtagtgtttggattgttaatgaaaaaatattatatgttcgttattccttgtattattgccacttatcttttgcttgataaaaatgcgttgttcttttttcttttggagggacaagatgaaaatatataatttgaattgattaaaattggtcgttactaaaatagtatagtaaccacaagtgattggcttataaatgaagtagaaatgctttttaatattccaaaatagagttccttttgatctgttggtgctgagccttggttaaaccagggagaaggggagcagaaaggaaacgttgttactgatgagtaccacagactcatcttaaaaaaaactctcattatggtgatcatagaattgaccatccaaactgggacactcttgagagtaaatggagggcattattaataattatcttgtaatgaacttaaatctggactgttccaggcaaaccagacttatcttgcaatatgagaatgctgacacaatgcaggaaagccagtttcccttttgttgatctacttgaccaagcaaaggggctgaaaaactgaataaggaaacaactttataagagaaacagtggtcttcaatcttttaaagacatgaaatcctatatggcattctgtctcagtgagtcagttaacaaatacgtatgtgcaacccttctgctagtagtgcacataagtgattatccctgccaggtatcgagttggaatatccagttatttcatgtcacacatcggcacgtatgatggtggtttggtcagatggataatacagcagacacacttagaacactcactgcactggtggctgttcattttgaggaactccaaagtcaattcaaggaaataaggaatgacctggaacaggccttagaaacaattgatttattccaatagttaaccactggctggctcccaactctaggtgataggcatctaattgagacatgtgtgagtcaatagccatcggggtcctttttggtgagaagaaataagacattttctcccttttaaagatcatctcttcagagctgcatggtaaatttgaatttccccattgttctctagagctaggtcaaaaaaacaactgtttcttttcttattccactattaataaattgaaagcttgctgtacaaaggcaacagcaacttaaaaaagaaaatctggacaatagatgtggactccaaggggccactgccatcccttcctgtgtgctctttttgacaagtaaatcactccagttagctgatgtcctgaaatgacatttgtacctgaggcaattcttattagagcttactcaggacttttcaaacatcaggacacacatagcaatttggatgttgtaaaactacgtgttacatttggagaggtcttgttgagaaggcaaaattttctaaatattttgatatcaatttgggtaaagaaaggaatacttttgttagaatgagaattaaagagaaaacaaaagaatcttggcaaaattttccctctgaaattacaaactttaggaacttttccagatgtatcgaatttaatttgacattgatgtcactcttcataccaagtgaatctattctcatgaactttgaacccatgttaattttggaccctataactaatttcctttctgtatcccatggtggtcaaagcagtaaaggagtttagagatacttagcaaatgccattcatatagtattgttagccaaactattattccttccttagaagttgatgtatcagaaaatttataagttatttgtatttatatataagtacatcagaacttgcccacatgataactcatgtttgctttaataaggaaaatatgttatttgaggttaattatatgatagtgaggaacattttacaattatttacagtgtttgacattaattgctgtcctatgatacagtagtaatgttaacagagagtttaatatgtttagcattatctttatggaatttatattcaccaatttcaggaaaaccaaccatagaactttataataggacagttataacctgactgaaccaaatccatcagcataatgactgtgtgttctgagaaatgcaaacaactttatgaaagtgtggtcatcttgacccccaaagagccacagtagctgtcaattattgagatttttaaatggtaaatattgcaaaagttaaacaagggtaccacaatatcatttataattgatgtcaatattagtagtccactttatgcttaaaataaaatcataaaaaatcaagttttaaggttatattttttaaaataatgaattttctatctctaggcaacatgtctttattattcaagctgaatgtttaagagagattttggtcttaaaggcttcacatcatgaaagtgtacatgcatatgcaagtgtgaattacgtggtatggatgtttgcttgtttattaactaaagatgtacagcaaactgcccgtttagagtcctgttaatattgatgtcctaacactgggtctgcttatgctagttcagtatttggtctaggcttcattttgatatgactgaattgcaatctatatttttaaaaagaaaaatcaaaatacattagggtttacttggttgtggcaaacaaacaaaaaatgctttcagtgttgaaatatctctattttccaaagatgataaactttcatcgttcttagcctacattgtcatttatatcaccaaatgagtttatagattaatgcaataaactttctaataaaaaa
//

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
This page is licensed under a Creative Commons Attribution 2.1 Japan License.