2024-03-29 15:39:15, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001393 3307 bp mRNA linear PRI 17-APR-2013 DEFINITION Homo sapiens extracellular matrix protein 2, female organ and adipocyte specific (ECM2), transcript variant 1, mRNA. ACCESSION NM_001393 VERSION NM_001393.3 GI:308818202 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 3307) AUTHORS Humphray,S.J., Oliver,K., Hunt,A.R., Plumb,R.W., Loveland,J.E., Howe,K.L., Andrews,T.D., Searle,S., Hunt,S.E., Scott,C.E., Jones,M.C., Ainscough,R., Almeida,J.P., Ambrose,K.D., Ashwell,R.I., Babbage,A.K., Babbage,S., Bagguley,C.L., Bailey,J., Banerjee,R., Barker,D.J., Barlow,K.F., Bates,K., Beasley,H., Beasley,O., Bird,C.P., Bray-Allen,S., Brown,A.J., Brown,J.Y., Burford,D., Burrill,W., Burton,J., Carder,C., Carter,N.P., Chapman,J.C., Chen,Y., Clarke,G., Clark,S.Y., Clee,C.M., Clegg,S., Collier,R.E., Corby,N., Crosier,M., Cummings,A.T., Davies,J., Dhami,P., Dunn,M., Dutta,I., Dyer,L.W., Earthrowl,M.E., Faulkner,L., Fleming,C.J., Frankish,A., Frankland,J.A., French,L., Fricker,D.G., Garner,P., Garnett,J., Ghori,J., Gilbert,J.G., Glison,C., Grafham,D.V., Gribble,S., Griffiths,C., Griffiths-Jones,S., Grocock,R., Guy,J., Hall,R.E., Hammond,S., Harley,J.L., Harrison,E.S., Hart,E.A., Heath,P.D., Henderson,C.D., Hopkins,B.L., Howard,P.J., Howden,P.J., Huckle,E., Johnson,C., Johnson,D., Joy,A.A., Kay,M., Keenan,S., Kershaw,J.K., Kimberley,A.M., King,A., Knights,A., Laird,G.K., Langford,C., Lawlor,S., Leongamornlert,D.A., Leversha,M., Lloyd,C., Lloyd,D.M., Lovell,J., Martin,S., Mashreghi-Mohammadi,M., Matthews,L., McLaren,S., McLay,K.E., McMurray,A., Milne,S., Nickerson,T., Nisbett,J., Nordsiek,G., Pearce,A.V., Peck,A.I., Porter,K.M., Pandian,R., Pelan,S., Phillimore,B., Povey,S., Ramsey,Y., Rand,V., Scharfe,M., Sehra,H.K., Shownkeen,R., Sims,S.K., Skuce,C.D., Smith,M., Steward,C.A., Swarbreck,D., Sycamore,N., Tester,J., Thorpe,A., Tracey,A., Tromans,A., Thomas,D.W., Wall,M., Wallis,J.M., West,A.P., Whitehead,S.L., Willey,D.L., Williams,S.A., Wilming,L., Wray,P.W., Young,L., Ashurst,J.L., Coulson,A., Blocker,H., Durbin,R., Sulston,J.E., Hubbard,T., Jackson,M.J., Bentley,D.R., Beck,S., Rogers,J. and Dunham,I. TITLE DNA sequence and analysis of human chromosome 9 JOURNAL Nature 429 (6990), 369-374 (2004) PUBMED 15164053 REFERENCE 2 (bases 1 to 3307) AUTHORS Nishiu,J., Tanaka,T. and Nakamura,Y. TITLE Identification of a novel gene (ECM2) encoding a putative extracellular matrix protein expressed predominantly in adipose and female-specific tissues and its chromosomal localization to 9q22.3 JOURNAL Genomics 52 (3), 378-381 (1998) PUBMED 9790758 REFERENCE 3 (bases 1 to 3307) AUTHORS Oritani,K., Kanakura,Y., Aoyama,K., Yokota,T., Copeland,N.G., Gilbert,D.J., Jenkins,N.A., Tomiyama,Y., Matsuzawa,Y. and Kincade,P.W. TITLE Matrix glycoprotein SC1/ECM2 augments B lymphopoiesis JOURNAL Blood 90 (9), 3404-3413 (1997) PUBMED 9345023 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from DC300418.1, AB011792.1 and BM972177.1. On Oct 16, 2010 this sequence version replaced gi:53759132. Summary: ECM2 encodes extracellular matrix protein 2, so named because it shares extensive similarity with known extracelluar matrix proteins. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2010]. Transcript Variant: This variant (1) represents the longest transcript and encodes the longest isoform (1). ##Evidence-Data-START## Transcript exon combination :: AB011792.1, AK312820.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025084, ERS025088 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-122 DC300418.1 1-122 123-3285 AB011792.1 9-3171 3286-3307 BM972177.1 1-22 c FEATURES Location/Qualifiers source 1..3307 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="9" /map="9q22.3" gene 1..3307 /gene="ECM2" /note="extracellular matrix protein 2, female organ and adipocyte specific" /db_xref="GeneID:1842" /db_xref="HGNC:3154" /db_xref="HPRD:09148" /db_xref="MIM:603479" exon 1..160 /gene="ECM2" /inference="alignment:Splign:1.39.8" misc_feature 26..28 /gene="ECM2" /note="upstream in-frame stop codon" exon 161..479 /gene="ECM2" /inference="alignment:Splign:1.39.8" CDS 188..2287 /gene="ECM2" /note="isoform 1 precursor is encoded by transcript variant 1; matrix glycoprotein SC1/ECM2" /codon_start=1 /product="extracellular matrix protein 2 isoform 1 precursor" /protein_id="NP_001384.1" /db_xref="GI:4557543" /db_xref="CCDS:CCDS6698.1" /db_xref="GeneID:1842" /db_xref="HGNC:3154" /db_xref="HPRD:09148" /db_xref="MIM:603479" /translation="
MKIAVLFCFFLLIIFQTDFGKNEEIPRKQRRKIYHRRLRKSSTSHKHRSNRQLGIQQTTVFTPVARLPIVNFDYSMEEKFESFSSFPGVESSYNVLPGKKGHCLVKGITMYNKAVWSPEPCTTCLCSDGRVLCDETMCHPQRCPQTVIPEGECCPVCSATVSYSLLSGIALNDRNEFSGDSSEQREPTNLLHKQLPPPQVGMDRIVRKEALQSEEDEEVKEEDTEQKRETPESRNQGQLYSEGDSRGGDRKQRPGEERRLAHQQQRQGREEEEDEEEEGEEGEEDEEDEEDPVRGDMFRMPSRSPLPAPPRGTLRLPSGCSLSYRTISCINAMLTQIPPLTAPQITSLELTGNSIASIPDEAFNGLPNLERLDLSKNNITSSGIGPKAFKLLKKLMRLNMDGNNLIQIPSQLPSTLEELKVNENNLQAIDEESLSDLNQLVTLELEGNNLSEANVNPLAFKPLKSLAYLRLGKNKFRIIPQGLPGSIEELYLENNQIEEITEICFNHTRKINVIVLRYNKIEENRIAPLAWINQENLESIDLSYNKLYHVPSYLPKSLLHLVLLGNQIERIPGYVFGHMEPGLEYLYLSFNKLADDGMDRVSFYGAYHSLRELFLDHNDLKSIPPGIQEMKALHFLRLNNNKIRNILPEEICNAEEDDDSNLEHLHLENNYIKIREIPSYTFSCIRSYSSIVLKPQNIK
" sig_peptide 188..247 /gene="ECM2" /inference="COORDINATES: ab initio prediction:SignalP:4.0" mat_peptide 248..2284 /gene="ECM2" /product="extracellular matrix protein 2 isoform 1" misc_feature 494..658 /gene="ECM2" /note="von Willebrand factor type C domain; Region: VWC; pfam00093" /db_xref="CDD:109161" misc_feature 1067..1075 /gene="ECM2" /inference="non-experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (O94769.1); Region: Cell attachment site (Potential)" misc_feature <1211..1615 /gene="ECM2" /note="Leucine-rich repeats (LRRs), ribonuclease inhibitor (RI)-like subfamily. LRRs are 20-29 residue sequence motifs present in many proteins that participate in protein-protein interactions and have different functions and cellular locations. LRRs correspond...; Region: LRR_RI; cl15309" /db_xref="CDD:199167" misc_feature 1217..1402 /gene="ECM2" /note="Leucine rich repeat; Region: LRR_8; pfam13855" /db_xref="CDD:206026" misc_feature order(1241..1243,1313..1315,1454..1456,1517..1519, 1523..1525,1595..1597) /gene="ECM2" /note="Substrate binding site [chemical binding]; other site" /db_xref="CDD:29015" misc_feature 1289..1351 /gene="ECM2" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (O94769.1); Region: LRR 1" misc_feature 1367..1432 /gene="ECM2" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (O94769.1); Region: LRR 2" misc_feature 1433..1615 /gene="ECM2" /note="Leucine rich repeat; Region: LRR_8; pfam13855" /db_xref="CDD:206026" misc_feature 1433..1495 /gene="ECM2" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (O94769.1); Region: LRR 3" misc_feature 1502..1564 /gene="ECM2" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (O94769.1); Region: LRR 4" misc_feature 1580..1639 /gene="ECM2" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (O94769.1); Region: LRR 5" misc_feature 1643..1828 /gene="ECM2" /note="Leucine rich repeat; Region: LRR_8; pfam13855" /db_xref="CDD:206026" misc_feature 1643..1708 /gene="ECM2" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (O94769.1); Region: LRR 6" misc_feature 1715..1777 /gene="ECM2" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (O94769.1); Region: LRR 7" misc_feature 1793..1966 /gene="ECM2" /note="Leucine rich repeat; Region: LRR_8; pfam13855" /db_xref="CDD:206026" misc_feature 1793..1858 /gene="ECM2" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (O94769.1); Region: LRR 8" misc_feature 1859..1921 /gene="ECM2" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (O94769.1); Region: LRR 9" misc_feature 1928..2062 /gene="ECM2" /note="Leucine Rich repeats (2 copies); Region: LRR_4; pfam12799" /db_xref="CDD:205079" misc_feature 1931..1993 /gene="ECM2" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (O94769.1); Region: LRR 10" misc_feature 2012..2077 /gene="ECM2" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (O94769.1); Region: LRR 11" misc_feature 2081..2146 /gene="ECM2" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (O94769.1); Region: LRR 12" misc_feature 2168..2239 /gene="ECM2" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (O94769.1); Region: LRR 13" variation complement(245) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:373531348" variation complement(337) /gene="ECM2" /replace="a" /replace="c" /db_xref="dbSNP:199523075" variation complement(354) /gene="ECM2" /replace="a" /replace="c" /db_xref="dbSNP:10120210" variation complement(372) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:137948457" variation complement(417) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:200534289" variation complement(426) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:150291467" variation complement(463) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:9299405" variation complement(474) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:201265258" exon 480..668 /gene="ECM2" /inference="alignment:Splign:1.39.8" variation complement(513) /gene="ECM2" /replace="c" /replace="g" /db_xref="dbSNP:35496743" variation complement(529) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:143418555" variation complement(537) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:149220459" variation complement(544) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:34729575" variation complement(622) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:201771443" variation complement(651) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:147710026" variation complement(652) /gene="ECM2" /replace="g" /replace="t" /db_xref="dbSNP:968040" variation complement(660) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:368912147" variation complement(667) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:139951554" exon 669..1241 /gene="ECM2" /inference="alignment:Splign:1.39.8" variation complement(683) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:147912487" variation complement(699) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:200349130" variation complement(706) /gene="ECM2" /replace="a" /replace="t" /db_xref="dbSNP:371633512" variation complement(747) /gene="ECM2" /replace="c" /replace="g" /db_xref="dbSNP:149769253" variation complement(754) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:201071759" variation complement(762) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:139720616" variation complement(792) /gene="ECM2" /replace="g" /replace="t" /db_xref="dbSNP:200225062" variation complement(797) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:368116708" variation complement(798) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:34758505" variation complement(812) /gene="ECM2" /replace="c" /replace="g" /db_xref="dbSNP:13293047" variation complement(813) /gene="ECM2" /replace="a" /replace="t" /db_xref="dbSNP:200124000" variation complement(816) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:375328673" variation complement(825) /gene="ECM2" /replace="a" /replace="c" /db_xref="dbSNP:13291847" variation complement(826) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:372289924" variation complement(835) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:368303849" variation complement(851) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:142198335" variation complement(857) /gene="ECM2" /replace="a" /replace="c" /db_xref="dbSNP:13298061" variation complement(858) /gene="ECM2" /replace="a" /replace="c" /db_xref="dbSNP:376085476" variation complement(868) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:182133503" variation complement(896) /gene="ECM2" /replace="c" /replace="g" /db_xref="dbSNP:145991428" variation complement(902) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:367636482" variation complement(918) /gene="ECM2" /replace="a" /replace="t" /db_xref="dbSNP:13297924" variation complement(976) /gene="ECM2" /replace="c" /replace="g" /db_xref="dbSNP:374472469" variation complement(983) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:142591312" variation complement(1001..1002) /gene="ECM2" /replace="" /replace="gtg" /db_xref="dbSNP:200095306" variation complement(1007) /gene="ECM2" /replace="c" /replace="g" /db_xref="dbSNP:137929518" variation complement(1009) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:34355623" variation complement(1019) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:149244773" variation complement(1062) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:369927306" variation complement(1082) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:138357265" variation complement(1083) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:372997619" variation complement(1095) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:143789386" variation complement(1102) /gene="ECM2" /replace="g" /replace="t" /db_xref="dbSNP:41280067" variation complement(1122) /gene="ECM2" /replace="g" /replace="t" /db_xref="dbSNP:142608064" variation complement(1130) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:138567683" variation complement(1141) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:148975367" variation complement(1203) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:201012391" variation complement(1217) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:147083553" variation complement(1234) /gene="ECM2" /replace="c" /replace="g" /db_xref="dbSNP:372699831" exon 1242..1357 /gene="ECM2" /inference="alignment:Splign:1.39.8" variation complement(1247) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:141793116" variation complement(1253) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:142186054" variation complement(1309) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:73651314" variation complement(1312) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:2296667" variation complement(1338) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:199972367" variation complement(1344) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:146339911" exon 1358..1493 /gene="ECM2" /inference="alignment:Splign:1.39.8" variation complement(1373) /gene="ECM2" /replace="a" /replace="t" /db_xref="dbSNP:139215803" variation complement(1377) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:41278707" variation complement(1421) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:370587410" variation complement(1460) /gene="ECM2" /replace="a" /replace="c" /db_xref="dbSNP:142108843" variation complement(1470) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:376172195" variation complement(1474) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:146040741" variation complement(1480) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:113660659" variation complement(1486) /gene="ECM2" /replace="g" /replace="t" /db_xref="dbSNP:144093801" exon 1494..1651 /gene="ECM2" /inference="alignment:Splign:1.39.8" variation complement(1528) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:35161698" variation complement(1541) /gene="ECM2" /replace="c" /replace="g" /db_xref="dbSNP:373455336" variation complement(1549) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:369126996" variation complement(1553) /gene="ECM2" /replace="a" /replace="c" /db_xref="dbSNP:199745267" variation complement(1592) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:150773107" variation complement(1595) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:376333101" variation complement(1627) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:141184307" variation complement(1639) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:148225586" variation complement(1651) /gene="ECM2" /replace="g" /replace="t" /db_xref="dbSNP:373635817" exon 1652..1791 /gene="ECM2" /inference="alignment:Splign:1.39.8" variation complement(1697) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:369347015" variation complement(1708) /gene="ECM2" /replace="a" /replace="t" /db_xref="dbSNP:143859115" variation complement(1737) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:372302066" exon 1792..2118 /gene="ECM2" /inference="alignment:Splign:1.39.8" variation complement(1806) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:376628552" variation complement(1814..1815) /gene="ECM2" /replace="" /replace="c" /db_xref="dbSNP:34868349" variation complement(1840) /gene="ECM2" /replace="g" /replace="t" /db_xref="dbSNP:199713916" variation complement(1882) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:143452414" variation complement(1895) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:199600306" variation complement(1900) /gene="ECM2" /replace="c" /replace="g" /db_xref="dbSNP:373764507" variation complement(1911) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:34518968" variation complement(1948) /gene="ECM2" /replace="a" /replace="c" /db_xref="dbSNP:147126273" variation complement(1972) /gene="ECM2" /replace="a" /replace="t" /db_xref="dbSNP:141859598" variation complement(1998) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:201745324" variation complement(2014) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:186648835" variation complement(2038) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:138868045" variation complement(2057) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:150249574" variation complement(2069) /gene="ECM2" /replace="a" /replace="c" /db_xref="dbSNP:140976209" variation complement(2116) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:370627896" variation complement(2117) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:151070730" variation complement(2118) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:200394678" exon 2119..3290 /gene="ECM2" /inference="alignment:Splign:1.39.8" variation complement(2145) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:188295382" variation complement(2153) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:201652423" STS 2160..2354 /gene="ECM2" /standard_name="RH69754" /db_xref="UniSTS:76501" variation complement(2171) /gene="ECM2" /replace="a" /replace="c" /db_xref="dbSNP:371904059" variation complement(2182) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:202159188" variation complement(2231) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:144194365" variation complement(2248) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:375516326" variation complement(2250) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:200233948" variation complement(2261) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:183564221" variation complement(2316) /gene="ECM2" /replace="c" /replace="g" /db_xref="dbSNP:371188020" variation complement(2319) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:191738373" variation complement(2325) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:376951503" variation complement(2453) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:189401619" variation complement(2545) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:369858665" variation complement(2658..2659) /gene="ECM2" /replace="" /replace="t" /db_xref="dbSNP:35985375" variation complement(2698) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:79708497" variation complement(2759) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:185286072" variation complement(2765) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:10429459" variation complement(2808) /gene="ECM2" /replace="g" /replace="t" /db_xref="dbSNP:150099514" variation complement(2839) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:192990935" variation complement(2887) /gene="ECM2" /replace="a" /replace="g" /db_xref="dbSNP:41278705" variation complement(2931) /gene="ECM2" /replace="a" /replace="t" /db_xref="dbSNP:183520336" variation complement(2978) /gene="ECM2" /replace="c" /replace="t" /db_xref="dbSNP:41278703" STS 3148..3273 /gene="ECM2" /standard_name="SHGC-34584" /db_xref="UniSTS:81055" STS 3148..3267 /gene="ECM2" /standard_name="RH47432" /db_xref="UniSTS:17932" polyA_signal 3268..3273 /gene="ECM2" polyA_site 3290 /gene="ECM2" ORIGIN
gggaggcagttattttagattttactaagaagttcagcaaatacttttcaacattcccttctgtcctttctttgtttttaaagaaagctctgattttgtttcattttcagctggagacttaaatgacaccaagcaaagcctacttagtttagatctccagaaattggctggtggaaaaaaatcaaacatgaagattgcagttttgttttgtttttttctgcttatcatttttcaaactgactttggaaaaaatgaagaaattcctaggaagcaaaggaggaagatctaccacagaaggttgaggaaaagttcaacctcacacaagcacagatcaaacagacagcttggaattcagcaaacaacagtttttacaccagtagcaagacttcctattgttaactttgattatagcatggaggaaaagtttgaatccttttcaagttttcctggagtagaatcaagttataatgtgttaccaggaaagaagggacactgtttggtaaagggcataaccatgtacaacaaagctgtgtggtcgcctgagccctgcactacctgcctctgctcagatggaagagttctttgtgatgaaaccatgtgccatccccagaggtgcccccaaacagttatacctgaaggggaatgctgcccggtctgctccgctactgtctcctattctctactcagtggtatagcattaaatgatagaaatgaattttctggtgattcttcagaacaaagagaacctaccaatttacttcataagcaactgccacctcctcaggtgggaatggaccgaatagtaagaaaagaagcacttcaatctgaggaggatgaagaagtgaaagaagaagatacagagcaaaagagagagacccctgaatctagaaatcaggggcaactttacagtgagggggacagcagaggaggagacagaaagcagaggcctggagaggagaggaggctggcacaccagcaacaacgccaaggaagggaggaggaggaggatgaggaggaggagggtgaggagggtgaggaggatgaggaggacgaggaggacccggtaagaggagatatgttccgaatgccctctcgatccccgcttcctgctcctcccagaggcacactgcgcctgccaagcgggtgctctctgtcctacaggaccatcagctgcatcaacgccatgcttacccagataccaccgctgacagcaccacagataacaagtctggagctcactggcaattccatcgcctccatcccagatgaagcatttaatggattaccaaatttggaaaggcttgatctgagtaaaaataatatcacttcttcaggcataggtccaaaagcattcaagcttctgaagaagttaatgcgtttgaatatggatggaaataatttgatacagattccttcacaattgccatctacattagaagaacttaaagtcaatgagaacaatcttcaggctatcgatgaagaaagtttatcagacttaaatcagttggtcaccttagaattggaaggaaacaatctcagtgaagccaatgtcaatcctttagctttcaaacctttgaagagcctagcctacttgcgtctgggaaaaaataaatttagaattataccgcagggtcttcctggttctattgaggaattatacctagaaaataaccaaattgaagaaataactgaaatttgtttcaatcataccagaaagatcaatgtcattgtactacgttataacaaaattgaagaaaataggattgctcctttagcctggataaatcaagaaaatctagaatccattgatctctcctacaacaagctctatcacgtcccgtcctatctacccaagtccttgctgcacctagtactccttgggaaccagattgaacggatccctggctatgtgtttggccacatggaaccaggcctggaatacttgtacctgtcatttaacaaacttgctgatgatggcatggaccgtgtctccttctatggggcatatcattctctgagagaattatttctggatcacaatgacttaaaatctataccacctgggatacaagaaatgaaagcactacattttctgaggctgaacaacaacaagatacggaacattcttccagaagaaatttgcaatgctgaagaggatgatgactcaaatctggaacatcttcatcttgaaaacaattatattaaaattagagaaataccatcttacacattttcatgcataagatcatactcaagtatcgttcttaaaccacaaaacatcaagtaattccaagttttcctttgctgtttataaactttactcatgtatttgtagtagctgcatttgtcattaataagagagacataatcctcctgttatactcagtatcattatatgctagtcaacctgattcactaacacacagatgaacaaccaaaatatacctaaaaggtatagtctctaggagttttattaatagtaaaggtaaaatctctcagtttcctacctctagaaagaggccatctcactagaataggatattatgcatactgagctagaccagaagagtctggaacaaaataaacacagcctttataatcaacttgaatactggtgttagctgagaactctgtaagtccctttaaaaattatgtatcttttggttcaagattaagaagcataatgacaacaaaaaaagcaggcagaatttatgaataagtgttgtttattattaaaacaataatttgttaatttcttataaggtcctgtgctataattactggtataaatataactgaatattggggtagctttcatttcttccattaattacatgtgtaaaattaaaacactactgtaatgttaatttcctggttttgaaaatcatattatggttatgtacattgttaacattaaggaaagctggcagaagggtgtgcataaattctatactctttttgaaacttttctataattctaaaattattttttaaagttaaacagtatattaagattaccttcactattcctcactcaagattaagacattttttgaaaagcagtagagtttgcttaaaatacaaattaattattcttgactataaccttgtaaaggtaaatctaatgtataaatttttgaaaaattttgcaccactggtcatagcatctatctcctttgccttaatttactgaaatacatcattttattcggttcaattgaaataaagctatgtctttactatgtattggccctaccaaaatcatatattaaaattttctaacataatgaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:1842 -> Molecular function: GO:0005178 [integrin binding] evidence: TAS GeneID:1842 -> Molecular function: GO:0008201 [heparin binding] evidence: IEA GeneID:1842 -> Molecular function: GO:0070052 [collagen V binding] evidence: IEA GeneID:1842 -> Biological process: GO:0007160 [cell-matrix adhesion] evidence: TAS GeneID:1842 -> Biological process: GO:0010811 [positive regulation of cell-substrate adhesion] evidence: IEA GeneID:1842 -> Biological process: GO:0030198 [extracellular matrix organization] evidence: IEA GeneID:1842 -> Cellular component: GO:0005578 [proteinaceous extracellular matrix] evidence: TAS GeneID:1842 -> Cellular component: GO:0005614 [interstitial matrix] evidence: IEA
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