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2025-05-09 19:11:22, 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 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
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