2024-03-29 21:22:14, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_021111 4427 bp mRNA linear PRI 24-JUN-2013 DEFINITION Homo sapiens reversion-inducing-cysteine-rich protein with kazal motifs (RECK), mRNA. ACCESSION NM_021111 VERSION NM_021111.2 GI:207029343 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 4427) AUTHORS Chiang,C.H., Hou,M.F. and Hung,W.C. TITLE Up-regulation of miR-182 by beta-catenin in breast cancer increases tumorigenicity and invasiveness by targeting the matrix metalloproteinase inhibitor RECK JOURNAL Biochim. Biophys. Acta 1830 (4), 3067-3076 (2013) PUBMED 23333633 REMARK GeneRIF: inverse association between miR-182 and RECK was demonstrated in breast tumor tissues REFERENCE 2 (bases 1 to 4427) AUTHORS Xin,C., Buhe,B., Hongting,L., Chuanmin,Y., Xiwei,H., Hong,Z., Lulu,H., Qian,D. and Renjie,W. TITLE MicroRNA-15a promotes neuroblastoma migration by targeting reversion-inducing cysteine-rich protein with Kazal motifs (RECK) and regulating matrix metalloproteinase-9 expression JOURNAL FEBS J. 280 (3), 855-866 (2013) PUBMED 23176145 REMARK GeneRIF: Findings indicate thet the miR-15a-RECK-matrix metalloproteinase-9 axis in neuroblastoma (NB) progression, especially in NB migration and invasion. REFERENCE 3 (bases 1 to 4427) 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 4 (bases 1 to 4427) AUTHORS Shen,B., Chen,J., Zheng,M.Q., Xu,X.Y., Wei,D. and Feng,J.F. TITLE [Expression and significance of HER-2/neu mRNA and RECK mRNA in breast carcinoma tissue] JOURNAL Zhonghua Shi Yan He Lin Chuang Bing Du Xue Za Zhi 26 (4), 279-281 (2012) PUBMED 23189844 REMARK GeneRIF: The level of HER-2/neu mRNA was higher and RECK mRNA was lower in breast carcinoma than homologous paraneoplastic breast tissue. REFERENCE 5 (bases 1 to 4427) AUTHORS Hirata,H., Ueno,K., Shahryari,V., Tanaka,Y., Tabatabai,Z.L., Hinoda,Y. and Dahiya,R. TITLE Oncogenic miRNA-182-5p targets Smad4 and RECK in human bladder cancer JOURNAL PLoS ONE 7 (11), E51056 (2012) PUBMED 23226455 REMARK GeneRIF: miR-182-5p plays an important role as an oncogene by knocking down RECK and Smad4, resulting in activation of the Wnt-beta-catenin signaling pathway in bladder cancer. REFERENCE 6 (bases 1 to 4427) AUTHORS Masui,T., Doi,R., Koshiba,T., Fujimoto,K., Tsuji,S., Nakajima,S., Koizumi,M., Toyoda,E., Tulachan,S., Ito,D., Kami,K., Mori,T., Wada,M., Noda,M. and Imamura,M. TITLE RECK expression in pancreatic cancer: its correlation with lower invasiveness and better prognosis JOURNAL Clin. Cancer Res. 9 (5), 1779-1784 (2003) PUBMED 12738734 REMARK GeneRIF: High RECK protein is associated with invasiveness of pancreatic cancer by MMP-2 activation REFERENCE 7 (bases 1 to 4427) AUTHORS Eisenberg,I., Hochner,H., Sadeh,M., Argov,Z. and Mitrani-Rosenbaum,S. TITLE Establishment of the genomic structure and identification of thirteen single-nucleotide polymorphisms in the human RECK gene JOURNAL Cytogenet. Genome Res. 97 (1-2), 58-61 (2002) PUBMED 12438739 REMARK GeneRIF: Four SNPs were identified in the coding region of the gene (exons 1, 9, 13 and 15), and the remaining nine in introns 5, 8, 10, 12, 15 and 17. REFERENCE 8 (bases 1 to 4427) AUTHORS Oh,J., Takahashi,R., Kondo,S., Mizoguchi,A., Adachi,E., Sasahara,R.M., Nishimura,S., Imamura,Y., Kitayama,H., Alexander,D.B., Ide,C., Horan,T.P., Arakawa,T., Yoshida,H., Nishikawa,S., Itoh,Y., Seiki,M., Itohara,S., Takahashi,C. and Noda,M. TITLE The membrane-anchored MMP inhibitor RECK is a key regulator of extracellular matrix integrity and angiogenesis JOURNAL Cell 107 (6), 789-800 (2001) PUBMED 11747814 REFERENCE 9 (bases 1 to 4427) AUTHORS Takahashi,C., Sheng,Z., Horan,T.P., Kitayama,H., Maki,M., Hitomi,K., Kitaura,Y., Takai,S., Sasahara,R.M., Horimoto,A., Ikawa,Y., Ratzkin,B.J., Arakawa,T. and Noda,M. TITLE Regulation of matrix metalloproteinase-9 and inhibition of tumor invasion by the membrane-anchored glycoprotein RECK JOURNAL Proc. Natl. Acad. Sci. U.S.A. 95 (22), 13221-13226 (1998) PUBMED 9789069 REFERENCE 10 (bases 1 to 4427) AUTHORS Gerstein,M. TITLE Measurement of the effectiveness of transitive sequence comparison, through a third 'intermediate' sequence JOURNAL Bioinformatics 14 (8), 707-714 (1998) PUBMED 9789096 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AK292653.1, D50406.1 and BC050306.1. On Sep 27, 2008 this sequence version replaced gi:11863155. Summary: The protein encoded by this gene is a cysteine-rich, extracellular protein with protease inhibitor-like domains whose expression is suppressed strongly in many tumors and cells transformed by various kinds of oncogenes. In normal cells, this membrane-anchored glycoprotein may serve as a negative regulator for matrix metalloproteinase-9, a key enzyme involved in tumor invasion and metastasis. [provided by RefSeq, Jul 2008]. 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 :: AK292653.1, D50406.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025081, ERS025083 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-6 AK292653.1 1-6 7-4117 D50406.1 30-4140 4118-4427 BC050306.1 4244-4553 FEATURES Location/Qualifiers source 1..4427 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="9" /map="9p13.3" gene 1..4427 /gene="RECK" /gene_synonym="ST15" /note="reversion-inducing-cysteine-rich protein with kazal motifs" /db_xref="GeneID:8434" /db_xref="HGNC:11345" /db_xref="HPRD:05567" /db_xref="MIM:605227" exon 1..186 /gene="RECK" /gene_synonym="ST15" /inference="alignment:Splign:1.39.8" variation 17..18 /gene="RECK" /gene_synonym="ST15" /replace="" /replace="ta" /db_xref="dbSNP:373891869" variation 24 /gene="RECK" /gene_synonym="ST15" /replace="g" /replace="t" /db_xref="dbSNP:143148105" variation 51 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="g" /db_xref="dbSNP:368806096" variation 64 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:147477093" CDS 87..3002 /gene="RECK" /gene_synonym="ST15" /note="suppression of tumorigenicity 5 (reversion-inducing-cysteine-rich protein with kazal motifs); membrane-anchored glycoprotein (metastasis and invasion); suppression of tumorigenicity 15 (reversion-inducing-cysteine-rich protein with kazal motifs); reversion-inducing cysteine-rich protein with Kazal motifs; suppressor of tumorigenicity 15 protein" /codon_start=1 /product="reversion-inducing cysteine-rich protein with Kazal motifs precursor" /protein_id="NP_066934.1" /db_xref="GI:11863156" /db_xref="CCDS:CCDS6597.1" /db_xref="GeneID:8434" /db_xref="HGNC:11345" /db_xref="HPRD:05567" /db_xref="MIM:605227" /translation="
MATVRASLRGALLLLLAVAGVAEVAGGLAPGSAGALCCNHSKDNQMCRDVCEQIFSSKSESRLKHLLQRAPDYCPETMVEIWNCMNSSLPGVFKKSDGWVGLGCCELAIALECRQACKQASSKNDISKVCRKEYENALFSCISRNEMGSVCCSYAGHHTNCREYCQAIFRTDSSPGPSQIKAVENYCASISPQLIHCVNNYTQSYPMRNPTDSLYCCDRAEDHACQNACKRILMSKKTEMEIVDGLIEGCKTQPLPQDPLWQCFLESSQSVHPGVTVHPPPSTGLDGAKLHCCSKANTSTCRELCTKLYSMSWGNTQSWQEFDRFCEYNPVEVSMLTCLADVREPCQLGCRNLTYCTNFNNRPTELFRSCNAQSDQGAMNDMKLWEKGSIKMPFINIPVLDIKKCQPEMWKAIACSLQIKPCHSKSRGSIICKSDCVEILKKCGDQNKFPEDHTAESICELLSPTDDLKNCIPLDTYLRPSTLGNIVEEVTHPCNPNPCPANELCEVNRKGCPSGDPCLPYFCVQGCKLGEASDFIVRQGTLIQVPSSAGEVGCYKICSCGQSGLLENCMEMHCIDLQKSCIVGGKRKSHGTSFSIDCNVCSCFAGNLVCSTRLCLSEHSSEDDRRTFTGLPCNCADQFVPVCGQNGRTYPSACIARCVGLQDHQFEFGSCMSKDPCNPNPCQKNQRCIPKPQVCLTTFDKFGCSQYECVPRQLACDQVQDPVCDTDHMEHNNLCTLYQRGKSLSYKGPCQPFCRATEPVCGHNGETYSSVCAAYSDRVAVDYYGDCQAVGVLSEHSSVAECASVKCPSLLAAGCKPIIPPGACCPLCAGMLRVLFDKEKLDTIAKVTNKKPITVLEILQKIRMHVSVPQCDVFGYFSIESEIVILIIPVDHYPKALQIEACNKEAEKIESLINSDSPTLASHVPLSALIISQVQVSSSVPSAGVRARPSCHSLLLPLSLGLALHLLWTYN
" sig_peptide 87..164 /gene="RECK" /gene_synonym="ST15" mat_peptide 165..2999 /gene="RECK" /gene_synonym="ST15" /product="reversion-inducing cysteine-rich protein with Kazal motifs" misc_feature 195..1100 /gene="RECK" /gene_synonym="ST15" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (O95980.1); Region: 5 X Knot repeats" variation 124 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:17855037" variation 135 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:139893051" variation 141 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:17855036" variation 156 /gene="RECK" /gene_synonym="ST15" /replace="g" /replace="t" /db_xref="dbSNP:201017437" variation 175 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:373799395" exon 187..245 /gene="RECK" /gene_synonym="ST15" /inference="alignment:Splign:1.39.8" variation 194 /gene="RECK" /gene_synonym="ST15" /replace="g" /replace="t" /db_xref="dbSNP:147362697" variation 227 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:373725096" variation 230 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:58611653" exon 246..320 /gene="RECK" /gene_synonym="ST15" /inference="alignment:Splign:1.39.8" variation 271 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:374518021" exon 321..357 /gene="RECK" /gene_synonym="ST15" /inference="alignment:Splign:1.39.8" exon 358..443 /gene="RECK" /gene_synonym="ST15" /inference="alignment:Splign:1.39.8" variation 384 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:371801859" variation 426 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:200440946" variation 427 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:374243748" exon 444..491 /gene="RECK" /gene_synonym="ST15" /inference="alignment:Splign:1.39.8" exon 492..525 /gene="RECK" /gene_synonym="ST15" /inference="alignment:Splign:1.39.8" exon 526..723 /gene="RECK" /gene_synonym="ST15" /inference="alignment:Splign:1.39.8" variation 553 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:201791836" variation 571 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:372609725" variation 594 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:1046658" variation 595 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:375748786" variation 612 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:200516550" variation 647 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:371411958" variation 649 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:373443775" variation 695 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:374632258" variation 697 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:140078883" variation 705 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:144022766" variation 718 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:144381566" variation 719 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:377258060" exon 724..991 /gene="RECK" /gene_synonym="ST15" /inference="alignment:Splign:1.39.8" variation 800 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:148788190" variation 864 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:147873679" variation 868 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:142469900" variation 896 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:200048340" variation 909 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:16932912" variation 923 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:201898968" variation 935 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:201258733" variation 941 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:139106894" variation 963 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:370216203" variation 978 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:376825824" exon 992..1171 /gene="RECK" /gene_synonym="ST15" /inference="alignment:Splign:1.39.8" variation 1009 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:372625092" variation 1080 /gene="RECK" /gene_synonym="ST15" /replace="g" /replace="t" /db_xref="dbSNP:376008783" variation 1088 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:3736884" variation 1090 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:372033961" variation 1114 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:374907660" variation 1143 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:372176214" exon 1172..1384 /gene="RECK" /gene_synonym="ST15" /inference="alignment:Splign:1.39.8" variation 1215 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:139919356" variation 1218 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="g" /db_xref="dbSNP:4430169" variation 1232 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="g" /db_xref="dbSNP:144037912" variation 1323 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:146471055" variation 1365 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:189825349" exon 1385..1521 /gene="RECK" /gene_synonym="ST15" /inference="alignment:Splign:1.39.8" variation 1395 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:199723720" variation 1408 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:140988213" variation 1412 /gene="RECK" /gene_synonym="ST15" /replace="" /replace="a" /db_xref="dbSNP:71508012" variation 1472 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:143337188" variation 1479 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:145575211" variation 1509 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:148890313" exon 1522..1662 /gene="RECK" /gene_synonym="ST15" /inference="alignment:Splign:1.39.8" variation 1560 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:146554287" variation 1578 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:78749972" variation 1646 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:11788747" exon 1663..1851 /gene="RECK" /gene_synonym="ST15" /inference="alignment:Splign:1.39.8" variation 1671 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="g" /db_xref="dbSNP:148296262" variation 1699 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:202116020" variation 1744 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:141592531" variation 1751 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:41277085" variation 1763 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:138423971" variation 1830 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:199710956" variation 1833 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:375477269" variation 1850 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="t" /db_xref="dbSNP:112938194" exon 1852..1974 /gene="RECK" /gene_synonym="ST15" /inference="alignment:Splign:1.39.8" variation 1872 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:201016307" variation 1880 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:199987061" variation 1884 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:371492299" variation 1944 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:150659859" variation 1961 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="t" /db_xref="dbSNP:10972727" variation 1962 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:149420244" exon 1975..2146 /gene="RECK" /gene_synonym="ST15" /inference="alignment:Splign:1.39.8" variation 1979 /gene="RECK" /gene_synonym="ST15" /replace="g" /replace="t" /db_xref="dbSNP:144862936" variation 1988 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:376678481" variation 2029 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:139092872" variation 2036 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:144005841" variation 2049 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:369196726" variation 2094 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="t" /db_xref="dbSNP:369829569" variation 2106 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:374527319" variation 2141 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="c" /db_xref="dbSNP:145965365" exon 2147..2339 /gene="RECK" /gene_synonym="ST15" /inference="alignment:Splign:1.39.8" variation 2190 /gene="RECK" /gene_synonym="ST15" /replace="g" /replace="t" /db_xref="dbSNP:139849271" variation 2223 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="c" /db_xref="dbSNP:370905430" variation 2228 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:183480403" variation 2229 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:142114378" variation 2231 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:151184551" variation 2334 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:140337764" exon 2340..2550 /gene="RECK" /gene_synonym="ST15" /inference="alignment:Splign:1.39.8" variation 2343 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="t" /db_xref="dbSNP:149956466" variation 2348 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:147648443" variation 2364 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:141528795" variation 2391 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="t" /db_xref="dbSNP:372053108" variation 2413 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:150265796" variation 2414 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:147027096" variation 2421 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:371483607" variation 2429 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:369985868" variation 2430 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:138317907" variation 2437 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:199917585" variation 2453 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:374500095" variation 2480 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:200760523" variation 2486 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:142383795" variation 2491 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:143294934" variation 2501 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="c" /db_xref="dbSNP:377608152" variation 2512 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:148349008" variation 2537 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:141548175" variation 2540 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:369729608" variation 2547 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:373692210" exon 2551..2624 /gene="RECK" /gene_synonym="ST15" /inference="alignment:Splign:1.39.8" variation 2591 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:373948774" variation 2600 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:150899620" exon 2625..2780 /gene="RECK" /gene_synonym="ST15" /inference="alignment:Splign:1.39.8" variation 2635 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:371744677" variation 2639 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:138496550" variation 2663 /gene="RECK" /gene_synonym="ST15" /replace="g" /replace="t" /db_xref="dbSNP:201184262" variation 2674 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:375728854" variation 2676 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="t" /db_xref="dbSNP:139573143" variation 2704 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:143080722" variation 2742 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:145922032" variation 2744 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:139816613" variation 2778 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="c" /db_xref="dbSNP:189943108" exon 2781..4412 /gene="RECK" /gene_synonym="ST15" /inference="alignment:Splign:1.39.8" variation 2877 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:372729870" variation 2883 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="c" /db_xref="dbSNP:149268263" variation 2915 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:56680169" variation 2916 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:192974126" variation 2930 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:148449362" variation 2955 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:142634835" variation 2957 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:147618963" variation 2977 /gene="RECK" /gene_synonym="ST15" /replace="g" /replace="t" /db_xref="dbSNP:140581680" variation 2986 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:374233309" variation 2996 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="t" /db_xref="dbSNP:376167480" variation 3011 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:111613206" variation 3028 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:199717555" variation 3042 /gene="RECK" /gene_synonym="ST15" /replace="g" /replace="t" /db_xref="dbSNP:369357445" variation 3089 /gene="RECK" /gene_synonym="ST15" /replace="g" /replace="t" /db_xref="dbSNP:7042392" variation 3177 /gene="RECK" /gene_synonym="ST15" /replace="g" /replace="t" /db_xref="dbSNP:75612573" variation 3368 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="g" /db_xref="dbSNP:7026399" variation 3439 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="g" /db_xref="dbSNP:72729497" variation 3472 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:188686266" variation 3515 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:193004377" variation 3615 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:74725990" variation 3720 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:184771768" variation 3759 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:115985599" variation 3849 /gene="RECK" /gene_synonym="ST15" /replace="c" /replace="t" /db_xref="dbSNP:188011114" variation 3852 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:371106795" variation 3893..3895 /gene="RECK" /gene_synonym="ST15" /replace="" /replace="ttc" /db_xref="dbSNP:3070848" variation 3897..3899 /gene="RECK" /gene_synonym="ST15" /replace="" /replace="aag" /db_xref="dbSNP:5897628" variation 4010..4013 /gene="RECK" /gene_synonym="ST15" /replace="" /replace="ctga" /db_xref="dbSNP:10523829" variation 4100..4101 /gene="RECK" /gene_synonym="ST15" /replace="" /replace="t" /db_xref="dbSNP:201199618" variation 4129..4130 /gene="RECK" /gene_synonym="ST15" /replace="" /replace="ca" /db_xref="dbSNP:150780340" STS 4226..4372 /gene="RECK" /gene_synonym="ST15" /standard_name="RH70038" /db_xref="UniSTS:66152" variation 4248 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:191216848" variation 4349 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:201902123" variation 4362 /gene="RECK" /gene_synonym="ST15" /replace="a" /replace="g" /db_xref="dbSNP:183723576" polyA_signal 4388..4393 /gene="RECK" /gene_synonym="ST15" polyA_site 4412 /gene="RECK" /gene_synonym="ST15" ORIGIN
gcgcgagcggcggcggtagcggcggcagcggctgcggccaagctgggtccgagcatcccgcggctctggagccgcccggcccggacatggcgaccgtccgggcctctctgcgaggtgcgctgctccttctgctggccgtggcgggggtcgcggaggtggcagggggcctggctccgggcagtgcgggtgcattgtgttgtaatcattcaaaggataaccaaatgtgccgtgatgtatgtgaacagattttctcctcaaaaagtgaatcccgactaaaacatctgttgcagcgagccccagattattgcccagagacaatggttgaaatttggaattgtatgaattcatctttgccaggtgtgtttaagaagtctgatggctgggttggcttaggctgctgtgaactggctattgccttggagtgtcgacaggcatgcaagcaggcatcttcaaagaatgatatttccaaagtttgcagaaaagaatatgagaatgctcttttcagttgcattagcagaaatgaaatgggctcggtttgttgcagttatgcaggtcatcacacaaactgccgagaatactgtcaagccatttttcgaacagactcttctcctggtccatctcagataaaagcagtggaaaattattgcgcctctattagtccacaattaatacattgtgtgaacaattatactcaatcttatccaatgaggaacccaacggatagtttatattgctgtgacagagctgaagaccatgcttgccaaaatgcctgcaagagaatcctgatgtccaagaaaacggaaatggagattgttgatggtctcatcgagggttgtaagacccagcccttgcctcaagatcctctttggcaatgttttcttgaaagctcacaatctgttcaccctggagtcactgtacaccctcctccctctacaggcctcgatggggctaaattgcattgttgttctaaagcaaacacttcaacatgtagggaactctgcactaaactttacagcatgagctggggcaatacacagagttggcaagagtttgatcgcttttgtgaatataatccagtggaagtgtccatgttgacctgtttagcggatgtccgggaaccttgccagttgggctgtagaaaccttacttactgtactaattttaacaacaggccaacagaacttttcaggagttgtaatgcacagtcagatcaaggagccatgaatgacatgaagttgtgggagaaaggaagcataaagatgccatttatcaatatacctgttcttgatattaaaaagtgccagccagagatgtggaaagcaatagcttgttcactgcagattaaaccttgtcatagtaaatctcggggaagtattatttgcaaatcagattgtgtggagattcttaaaaaatgtggagaccagaacaaattccctgaagaccacacagctgaaagtatttgtgagcttctgtcacctacagatgatctgaagaattgtatacctttggatacatacctcaggccaagtactttaggtaacattgtagaagaagtgactcatccctgtaacccaaatccttgccctgccaatgagctctgtgaagtaaaccgaaaaggatgtccatctggagatccctgtcttccatacttttgtgttcaaggttgcaaactgggagaagcttctgatttcattgtccgtcaagggacactaatccaggtgccatcatctgcaggggaagttggttgttataaaatctgttcatgtggacaaagtggactcttagaaaactgtatggaaatgcactgtatagacctccagaagtcttgtattgttggaggaaaaagaaaaagtcatggaacatcctttagtattgactgcaatgtctgttcttgttttgctggcaatttggtgtgctctacccgcctttgcctcagtgagcacagttcagaagatgaccgtcgtaccttcacaggtctgccctgtaactgtgcagatcagtttgtccctgtatgtgggcagaatgggcgcacttaccccagtgcctgcattgctcgctgtgtgggcctccaagaccatcagtttgagtttggatcatgcatgtcaaaggatccatgtaatcctaatccctgccaaaaaaaccaaaggtgcatacccaaaccacaggtctgcctgacgacttttgataaatttggatgtagccagtatgagtgtgtaccaagacagctcgcgtgtgaccaggtccaagatcctgtttgtgacacagaccacatggagcacaacaatctctgcactttataccaaagaggaaaaagcctctcttacaaaggtccctgccagcccttttgcagagcaaccgagcccgtatgtgggcacaatggtgagacctacagcagtgtgtgtgctgcctactcggatcgcgtggcagtcgattactatggggactgccaggccgtcggagtcctctcagagcacagctccgtcgccgagtgtgcttctgtcaagtgtccttcgctcttggcagctggatgcaaacccatcatcccaccgggtgcttgttgcccattatgtgctgggatgttaagagttttatttgacaaagaaaaactggatactattgctaaggtaacaaataaaaagccaataacagttctggaaatacttcagaaaatccgcatgcacgtgtctgtcccacagtgtgatgtgtttggatacttcagcattgaatcagaaattgtgatcctgatcattcccgtcgatcactatccaaaagctctgcagattgaagcctgcaataaagaagcagagaagattgagtcccttatcaactctgacagcccgactttggcgtcccatgtccctctctctgccctcatcatttcccaggtacaggtctccagcagtgtgccatcggccggtgtcagggccaggccttcttgccactccctcctccttcccctcagcttgggccttgccttgcacttgctctggacatataactgactgcccacggaaagtgcagaatgctcctccacctcactctcctgccttgaaaaagacattcaggactgctggtttgtagttgaatattggccaaggaaaggcacatgtcacctctattcgccacacagtatttttttttttaatccgccaatattagtaggatttttgttttgtttttacaaatgttaaaatgtgttgttccaaatactaatgaaaacagaatgtctcttcctggtagaccactgccatatgatttacatttcctcaccataagggtcccccactctaaagcaaatttatcgctgggaaatgagatgaccactttttagaaagataattcactgtactatcaggttcacaaacttcatttcagagttctttttgaagtatttaaggttcccgttgcatttgttttgtttacagataattacctactctggctagaagctaggggtcccagtgaagagccactgccattaaagaatatgaaacatagataaaacatctttgaaattatgtaaattatgtaaattatcaggcaaatttgcattaaattacagaaatttaattcagaaccccaactactgtgttatgcaaaagcaagctgattaaatgacactcatataattatatgttgtaagcaacaggctcactggtcacggatttgtgtctgtgacttttgtgaaagggagaagtgacattgcatcaaagcatcttgcattatgcaatttttatattaaccagatatatattcatcggtattcatccaagttaaatgtagagtttttaaacatcaatctttaaaccaattgctgctacttatataattgccaaaaagtgaaataatgtgtagttcatgtaaataatacattatatttctattttattatgaagaaggtgaatagccatatttgtaaaatgacaatcatgtgtgttaacccagtgctttccattcgtgaaaacacatttgctttttgtgatatgcacaatgtagataagtgttctgtctgactttcttttttgatatagaagtataaagaattgtggtttatatatttaaaagtgtcaagctgagtattaaaatgtatgcatgttgtctaagaaattgaatactttgaatgtgtttcacagtttgaaataagctatttgatgtaatacttcttgtgtgtatgcacatgaacttagattttacatgaagtattttttcagtattatatgtaccctctgaaatacatagggatatgcgtattataccaaaatgttgctgaaaaatgggcacttaaagctttcagaatatgtcagtgctgatgtagcatgcttgttgcaattgccttttttctgtataaatgtctttaatgcaatatactggaaagcttttctattttaataaaaataatttttatatgatcaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:8434 -> Molecular function: GO:0004866 [endopeptidase inhibitor activity] evidence: IDA GeneID:8434 -> Molecular function: GO:0004867 [serine-type endopeptidase inhibitor activity] evidence: IEA GeneID:8434 -> Molecular function: GO:0008191 [metalloendopeptidase inhibitor activity] evidence: TAS GeneID:8434 -> Biological process: GO:0001955 [blood vessel maturation] evidence: IEA GeneID:8434 -> Biological process: GO:0007566 [embryo implantation] evidence: IEA GeneID:8434 -> Biological process: GO:0030198 [extracellular matrix organization] evidence: IEA GeneID:8434 -> Cellular component: GO:0005886 [plasma membrane] evidence: IEA GeneID:8434 -> Cellular component: GO:0016020 [membrane] evidence: TAS GeneID:8434 -> Cellular component: GO:0031225 [anchored to membrane] evidence: IEA
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