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2025-05-09 19:33:29, 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 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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