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2024-04-20 17:52:10, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001197295 3241 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens extracellular matrix protein 2, female organ and
adipocyte specific (ECM2), transcript variant 2, mRNA.
ACCESSION NM_001197295
VERSION NM_001197295.1 GI:308818203
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 3241)
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 3241)
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 3241)
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,
BX537976.1 and BM972177.1.
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 (2) uses an alternate in-frame
splice junction at the 5' end of an exon compared to variant 1. The
resulting isoform (2) has the same N- and C-termini but is shorter
compared to isoform 1.
##Evidence-Data-START##
Transcript exon combination :: AK296458.1 [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
123-354 AB011792.1 9-240
355-2052 BX537976.1 318-2015
2053-3219 AB011792.1 2005-3171
3220-3241 BM972177.1 1-22 c
FEATURES Location/Qualifiers
source 1..3241
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="9"
/map="9q22.3"
gene 1..3241
/gene="ECM2"
/note="extracellular matrix protein 2, female organ and
adipocyte specific"
/db_xref="GeneID:1842"
/db_xref="HGNC:3154"
/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..2221
/gene="ECM2"
/note="isoform 2 precursor is encoded by transcript
variant 2; matrix glycoprotein SC1/ECM2"
/codon_start=1
/product="extracellular matrix protein 2 isoform 2
precursor"
/protein_id="NP_001184224.1"
/db_xref="GI:308818204"
/db_xref="GeneID:1842"
/db_xref="HGNC:3154"
/db_xref="MIM:603479"
/translation="
MKIAVLFCFFLLIIFQTDFGKNEEIPRKQRRKIYHRRLRKSSTSHKHRSNRQLGIQQTTVFTPVARLPIVNFDYSMEEKFESFSSFPGVESSYNVLPGKKGHCLVKGITMYNKAVWSPEPCTTCLCSDGRVLCDETMCHPQRCPQTVIPEGECCPVCSATEQREPTNLLHKQLPPPQVGMDRIVRKEALQSEEDEEVKEEDTEQKRETPESRNQGQLYSEGDSRGGDRKQRPGEERRLAHQQQRQGREEEEDEEEEGEEGEEDEEDEEDPVRGDMFRMPSRSPLPAPPRGTLRLPSGCSLSYRTISCINAMLTQIPPLTAPQITSLELTGNSIASIPDEAFNGLPNLERLDLSKNNITSSGIGPKAFKLLKKLMRLNMDGNNLIQIPSQLPSTLEELKVNENNLQAIDEESLSDLNQLVTLELEGNNLSEANVNPLAFKPLKSLAYLRLGKNKFRIIPQGLPGSIEELYLENNQIEEITEICFNHTRKINVIVLRYNKIEENRIAPLAWINQENLESIDLSYNKLYHVPSYLPKSLLHLVLLGNQIERIPGYVFGHMEPGLEYLYLSFNKLADDGMDRVSFYGAYHSLRELFLDHNDLKSIPPGIQEMKALHFLRLNNNKIRNILPEEICNAEEDDDSNLEHLHLENNYIKIREIPSYTFSCIRSYSSIVLKPQNIK
"
sig_peptide 188..247
/gene="ECM2"
/inference="COORDINATES: ab initio prediction:SignalP:4.0"
mat_peptide 248..2218
/gene="ECM2"
/product="extracellular matrix protein 2 isoform 2"
misc_feature 494..658
/gene="ECM2"
/note="von Willebrand factor type C domain; Region: VWC;
pfam00093"
/db_xref="CDD:109161"
misc_feature <1145..1549
/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 1151..1336
/gene="ECM2"
/note="Leucine rich repeat; Region: LRR_8; pfam13855"
/db_xref="CDD:206026"
misc_feature order(1175..1177,1247..1249,1388..1390,1451..1453,
1457..1459,1529..1531)
/gene="ECM2"
/note="Substrate binding site [chemical binding]; other
site"
/db_xref="CDD:29015"
misc_feature 1367..1549
/gene="ECM2"
/note="Leucine rich repeat; Region: LRR_8; pfam13855"
/db_xref="CDD:206026"
misc_feature 1577..1762
/gene="ECM2"
/note="Leucine rich repeat; Region: LRR_8; pfam13855"
/db_xref="CDD:206026"
misc_feature 1790..1981
/gene="ECM2"
/note="Leucine rich repeat; Region: LRR_8; pfam13855"
/db_xref="CDD:206026"
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..1175
/gene="ECM2"
/inference="alignment:Splign:1.39.8"
variation complement(681)
/gene="ECM2"
/replace="c"
/replace="g"
/db_xref="dbSNP:149769253"
variation complement(688)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201071759"
variation complement(696)
/gene="ECM2"
/replace="a"
/replace="g"
/db_xref="dbSNP:139720616"
variation complement(726)
/gene="ECM2"
/replace="g"
/replace="t"
/db_xref="dbSNP:200225062"
variation complement(731)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:368116708"
variation complement(732)
/gene="ECM2"
/replace="a"
/replace="g"
/db_xref="dbSNP:34758505"
variation complement(746)
/gene="ECM2"
/replace="c"
/replace="g"
/db_xref="dbSNP:13293047"
variation complement(747)
/gene="ECM2"
/replace="a"
/replace="t"
/db_xref="dbSNP:200124000"
variation complement(750)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:375328673"
variation complement(759)
/gene="ECM2"
/replace="a"
/replace="c"
/db_xref="dbSNP:13291847"
variation complement(760)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:372289924"
variation complement(769)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:368303849"
variation complement(785)
/gene="ECM2"
/replace="a"
/replace="g"
/db_xref="dbSNP:142198335"
variation complement(791)
/gene="ECM2"
/replace="a"
/replace="c"
/db_xref="dbSNP:13298061"
variation complement(792)
/gene="ECM2"
/replace="a"
/replace="c"
/db_xref="dbSNP:376085476"
variation complement(802)
/gene="ECM2"
/replace="a"
/replace="g"
/db_xref="dbSNP:182133503"
variation complement(830)
/gene="ECM2"
/replace="c"
/replace="g"
/db_xref="dbSNP:145991428"
variation complement(836)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:367636482"
variation complement(852)
/gene="ECM2"
/replace="a"
/replace="t"
/db_xref="dbSNP:13297924"
variation complement(910)
/gene="ECM2"
/replace="c"
/replace="g"
/db_xref="dbSNP:374472469"
variation complement(917)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:142591312"
variation complement(935..936)
/gene="ECM2"
/replace=""
/replace="gtg"
/db_xref="dbSNP:200095306"
variation complement(941)
/gene="ECM2"
/replace="c"
/replace="g"
/db_xref="dbSNP:137929518"
variation complement(943)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:34355623"
variation complement(953)
/gene="ECM2"
/replace="a"
/replace="g"
/db_xref="dbSNP:149244773"
variation complement(996)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:369927306"
variation complement(1016)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:138357265"
variation complement(1017)
/gene="ECM2"
/replace="a"
/replace="g"
/db_xref="dbSNP:372997619"
variation complement(1029)
/gene="ECM2"
/replace="a"
/replace="g"
/db_xref="dbSNP:143789386"
variation complement(1036)
/gene="ECM2"
/replace="g"
/replace="t"
/db_xref="dbSNP:41280067"
variation complement(1056)
/gene="ECM2"
/replace="g"
/replace="t"
/db_xref="dbSNP:142608064"
variation complement(1064)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:138567683"
variation complement(1075)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:148975367"
variation complement(1137)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201012391"
variation complement(1151)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:147083553"
variation complement(1168)
/gene="ECM2"
/replace="c"
/replace="g"
/db_xref="dbSNP:372699831"
exon 1176..1291
/gene="ECM2"
/inference="alignment:Splign:1.39.8"
variation complement(1181)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:141793116"
variation complement(1187)
/gene="ECM2"
/replace="a"
/replace="g"
/db_xref="dbSNP:142186054"
variation complement(1243)
/gene="ECM2"
/replace="a"
/replace="g"
/db_xref="dbSNP:73651314"
variation complement(1246)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2296667"
variation complement(1272)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:199972367"
variation complement(1278)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:146339911"
exon 1292..1427
/gene="ECM2"
/inference="alignment:Splign:1.39.8"
variation complement(1307)
/gene="ECM2"
/replace="a"
/replace="t"
/db_xref="dbSNP:139215803"
variation complement(1311)
/gene="ECM2"
/replace="a"
/replace="g"
/db_xref="dbSNP:41278707"
variation complement(1355)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:370587410"
variation complement(1394)
/gene="ECM2"
/replace="a"
/replace="c"
/db_xref="dbSNP:142108843"
variation complement(1404)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:376172195"
variation complement(1408)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:146040741"
variation complement(1414)
/gene="ECM2"
/replace="a"
/replace="g"
/db_xref="dbSNP:113660659"
variation complement(1420)
/gene="ECM2"
/replace="g"
/replace="t"
/db_xref="dbSNP:144093801"
exon 1428..1585
/gene="ECM2"
/inference="alignment:Splign:1.39.8"
variation complement(1462)
/gene="ECM2"
/replace="a"
/replace="g"
/db_xref="dbSNP:35161698"
variation complement(1475)
/gene="ECM2"
/replace="c"
/replace="g"
/db_xref="dbSNP:373455336"
variation complement(1483)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:369126996"
variation complement(1487)
/gene="ECM2"
/replace="a"
/replace="c"
/db_xref="dbSNP:199745267"
variation complement(1526)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:150773107"
variation complement(1529)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:376333101"
variation complement(1561)
/gene="ECM2"
/replace="a"
/replace="g"
/db_xref="dbSNP:141184307"
variation complement(1573)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:148225586"
variation complement(1585)
/gene="ECM2"
/replace="g"
/replace="t"
/db_xref="dbSNP:373635817"
exon 1586..1725
/gene="ECM2"
/inference="alignment:Splign:1.39.8"
variation complement(1631)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:369347015"
variation complement(1642)
/gene="ECM2"
/replace="a"
/replace="t"
/db_xref="dbSNP:143859115"
variation complement(1671)
/gene="ECM2"
/replace="a"
/replace="g"
/db_xref="dbSNP:372302066"
exon 1726..2052
/gene="ECM2"
/inference="alignment:Splign:1.39.8"
variation complement(1740)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:376628552"
variation complement(1748..1749)
/gene="ECM2"
/replace=""
/replace="c"
/db_xref="dbSNP:34868349"
variation complement(1774)
/gene="ECM2"
/replace="g"
/replace="t"
/db_xref="dbSNP:199713916"
variation complement(1816)
/gene="ECM2"
/replace="a"
/replace="g"
/db_xref="dbSNP:143452414"
variation complement(1829)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:199600306"
variation complement(1834)
/gene="ECM2"
/replace="c"
/replace="g"
/db_xref="dbSNP:373764507"
variation complement(1845)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:34518968"
variation complement(1882)
/gene="ECM2"
/replace="a"
/replace="c"
/db_xref="dbSNP:147126273"
variation complement(1906)
/gene="ECM2"
/replace="a"
/replace="t"
/db_xref="dbSNP:141859598"
variation complement(1932)
/gene="ECM2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201745324"
variation complement(1948)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:186648835"
variation complement(1972)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:138868045"
variation complement(1991)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:150249574"
variation complement(2003)
/gene="ECM2"
/replace="a"
/replace="c"
/db_xref="dbSNP:140976209"
variation complement(2050)
/gene="ECM2"
/replace="a"
/replace="g"
/db_xref="dbSNP:370627896"
variation complement(2051)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:151070730"
variation complement(2052)
/gene="ECM2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200394678"
exon 2053..3224
/gene="ECM2"
/inference="alignment:Splign:1.39.8"
variation complement(2079)
/gene="ECM2"
/replace="a"
/replace="g"
/db_xref="dbSNP:188295382"
variation complement(2087)
/gene="ECM2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201652423"
STS 2094..2288
/gene="ECM2"
/standard_name="RH69754"
/db_xref="UniSTS:76501"
variation complement(2105)
/gene="ECM2"
/replace="a"
/replace="c"
/db_xref="dbSNP:371904059"
variation complement(2116)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:202159188"
variation complement(2165)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:144194365"
variation complement(2182)
/gene="ECM2"
/replace="a"
/replace="g"
/db_xref="dbSNP:375516326"
variation complement(2184)
/gene="ECM2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200233948"
variation complement(2195)
/gene="ECM2"
/replace="a"
/replace="g"
/db_xref="dbSNP:183564221"
variation complement(2250)
/gene="ECM2"
/replace="c"
/replace="g"
/db_xref="dbSNP:371188020"
variation complement(2253)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:191738373"
variation complement(2259)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:376951503"
variation complement(2387)
/gene="ECM2"
/replace="a"
/replace="g"
/db_xref="dbSNP:189401619"
variation complement(2479)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:369858665"
variation complement(2592..2593)
/gene="ECM2"
/replace=""
/replace="t"
/db_xref="dbSNP:35985375"
variation complement(2632)
/gene="ECM2"
/replace="a"
/replace="g"
/db_xref="dbSNP:79708497"
variation complement(2693)
/gene="ECM2"
/replace="a"
/replace="g"
/db_xref="dbSNP:185286072"
variation complement(2699)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:10429459"
variation complement(2742)
/gene="ECM2"
/replace="g"
/replace="t"
/db_xref="dbSNP:150099514"
variation complement(2773)
/gene="ECM2"
/replace="a"
/replace="g"
/db_xref="dbSNP:192990935"
variation complement(2821)
/gene="ECM2"
/replace="a"
/replace="g"
/db_xref="dbSNP:41278705"
variation complement(2865)
/gene="ECM2"
/replace="a"
/replace="t"
/db_xref="dbSNP:183520336"
variation complement(2912)
/gene="ECM2"
/replace="c"
/replace="t"
/db_xref="dbSNP:41278703"
STS 3082..3207
/gene="ECM2"
/standard_name="SHGC-34584"
/db_xref="UniSTS:81055"
STS 3082..3201
/gene="ECM2"
/standard_name="RH47432"
/db_xref="UniSTS:17932"
polyA_signal 3202..3207
/gene="ECM2"
polyA_site 3224
/gene="ECM2"
ORIGIN
gggaggcagttattttagattttactaagaagttcagcaaatacttttcaacattcccttctgtcctttctttgtttttaaagaaagctctgattttgtttcattttcagctggagacttaaatgacaccaagcaaagcctacttagtttagatctccagaaattggctggtggaaaaaaatcaaacatgaagattgcagttttgttttgtttttttctgcttatcatttttcaaactgactttggaaaaaatgaagaaattcctaggaagcaaaggaggaagatctaccacagaaggttgaggaaaagttcaacctcacacaagcacagatcaaacagacagcttggaattcagcaaacaacagtttttacaccagtagcaagacttcctattgttaactttgattatagcatggaggaaaagtttgaatccttttcaagttttcctggagtagaatcaagttataatgtgttaccaggaaagaagggacactgtttggtaaagggcataaccatgtacaacaaagctgtgtggtcgcctgagccctgcactacctgcctctgctcagatggaagagttctttgtgatgaaaccatgtgccatccccagaggtgcccccaaacagttatacctgaaggggaatgctgcccggtctgctccgctactgaacaaagagaacctaccaatttacttcataagcaactgccacctcctcaggtgggaatggaccgaatagtaagaaaagaagcacttcaatctgaggaggatgaagaagtgaaagaagaagatacagagcaaaagagagagacccctgaatctagaaatcaggggcaactttacagtgagggggacagcagaggaggagacagaaagcagaggcctggagaggagaggaggctggcacaccagcaacaacgccaaggaagggaggaggaggaggatgaggaggaggagggtgaggagggtgaggaggatgaggaggacgaggaggacccggtaagaggagatatgttccgaatgccctctcgatccccgcttcctgctcctcccagaggcacactgcgcctgccaagcgggtgctctctgtcctacaggaccatcagctgcatcaacgccatgcttacccagataccaccgctgacagcaccacagataacaagtctggagctcactggcaattccatcgcctccatcccagatgaagcatttaatggattaccaaatttggaaaggcttgatctgagtaaaaataatatcacttcttcaggcataggtccaaaagcattcaagcttctgaagaagttaatgcgtttgaatatggatggaaataatttgatacagattccttcacaattgccatctacattagaagaacttaaagtcaatgagaacaatcttcaggctatcgatgaagaaagtttatcagacttaaatcagttggtcaccttagaattggaaggaaacaatctcagtgaagccaatgtcaatcctttagctttcaaacctttgaagagcctagcctacttgcgtctgggaaaaaataaatttagaattataccgcagggtcttcctggttctattgaggaattatacctagaaaataaccaaattgaagaaataactgaaatttgtttcaatcataccagaaagatcaatgtcattgtactacgttataacaaaattgaagaaaataggattgctcctttagcctggataaatcaagaaaatctagaatccattgatctctcctacaacaagctctatcacgtcccgtcctatctacccaagtccttgctgcacctagtactccttgggaaccagattgaacggatccctggctatgtgtttggccacatggaaccaggcctggaatacttgtacctgtcatttaacaaacttgctgatgatggcatggaccgtgtctccttctatggggcatatcattctctgagagaattatttctggatcacaatgacttaaaatctataccacctgggatacaagaaatgaaagcactacattttctgaggctgaacaacaacaagatacggaacattcttccagaagaaatttgcaatgctgaagaggatgatgactcaaatctggaacatcttcatcttgaaaacaattatattaaaattagagaaataccatcttacacattttcatgcataagatcatactcaagtatcgttcttaaaccacaaaacatcaagtaattccaagttttcctttgctgtttataaactttactcatgtatttgtagtagctgcatttgtcattaataagagagacataatcctcctgttatactcagtatcattatatgctagtcaacctgattcactaacacacagatgaacaaccaaaatatacctaaaaggtatagtctctaggagttttattaatagtaaaggtaaaatctctcagtttcctacctctagaaagaggccatctcactagaataggatattatgcatactgagctagaccagaagagtctggaacaaaataaacacagcctttataatcaacttgaatactggtgttagctgagaactctgtaagtccctttaaaaattatgtatcttttggttcaagattaagaagcataatgacaacaaaaaaagcaggcagaatttatgaataagtgttgtttattattaaaacaataatttgttaatttcttataaggtcctgtgctataattactggtataaatataactgaatattggggtagctttcatttcttccattaattacatgtgtaaaattaaaacactactgtaatgttaatttcctggttttgaaaatcatattatggttatgtacattgttaacattaaggaaagctggcagaagggtgtgcataaattctatactctttttgaaacttttctataattctaaaattattttttaaagttaaacagtatattaagattaccttcactattcctcactcaagattaagacattttttgaaaagcagtagagtttgcttaaaatacaaattaattattcttgactataaccttgtaaaggtaaatctaatgtataaatttttgaaaaattttgcaccactggtcatagcatctatctcctttgccttaatttactgaaatacatcattttattcggttcaattgaaataaagctatgtctttactatgtattggccctaccaaaatcatatattaaaattttctaacataatgaaaaaaaaaaaaaaaaaa
//
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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@meso_cacase at
DBCLS
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