2024-04-25 10:14:36, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001042750 6186 bp mRNA linear PRI 17-APR-2013 DEFINITION Homo sapiens stromal antigen 2 (STAG2), transcript variant 2, mRNA. ACCESSION NM_001042750 VERSION NM_001042750.1 GI:112789527 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 6186) AUTHORS Chung,N.G., Kim,M.S., Yoo,N.J. and Lee,S.H. TITLE Somatic mutation of STAG2, an aneuploidy-related gene, is rare in acute leukemias JOURNAL Leuk. Lymphoma 53 (6), 1234-1235 (2012) PUBMED 22132872 REMARK GeneRIF: Somatic mutation of STAG2, an aneuploidy-related gene, is rare in acute leukemias. REFERENCE 2 (bases 1 to 6186) AUTHORS Kim,M.S., Kim,S.S., Je,E.M., Yoo,N.J. and Lee,S.H. TITLE Mutational and expressional analyses of STAG2 gene in solid cancers JOURNAL Neoplasma 59 (5), 524-529 (2012) PUBMED 22668012 REMARK GeneRIF: Low STAG2 expression and not mutation is associated with neoplasms. REFERENCE 3 (bases 1 to 6186) AUTHORS Solomon,D.A., Kim,T., Diaz-Martinez,L.A., Fair,J., Elkahloun,A.G., Harris,B.T., Toretsky,J.A., Rosenberg,S.A., Shukla,N., Ladanyi,M., Samuels,Y., James,C.D., Yu,H., Kim,J.S. and Waldman,T. TITLE Mutational inactivation of STAG2 causes aneuploidy in human cancer JOURNAL Science 333 (6045), 1039-1043 (2011) PUBMED 21852505 REMARK GeneRIF: study has shown that diverse human cancers harbor mutations in the X-linked chromatid cohesion gene STAG2 and that these mutations cause aneuploidy REFERENCE 4 (bases 1 to 6186) AUTHORS Xiao,T., Wallace,J. and Felsenfeld,G. TITLE Specific sites in the C terminus of CTCF interact with the SA2 subunit of the cohesin complex and are required for cohesin-dependent insulation activity JOURNAL Mol. Cell. Biol. 31 (11), 2174-2183 (2011) PUBMED 21444719 REMARK GeneRIF: results demonstrate specific sites on C terminus of CTCF are essential for cohesin binding and insulator function; only direct interaction between CTCF and cohesin involves contact with SA2, which is external to the cohesin ring REFERENCE 5 (bases 1 to 6186) AUTHORS Canudas,S. and Smith,S. TITLE Differential regulation of telomere and centromere cohesion by the Scc3 homologues SA1 and SA2, respectively, in human cells JOURNAL J. Cell Biol. 187 (2), 165-173 (2009) PUBMED 19822671 REMARK GeneRIF: cohesin(SA1) and cohesin(SA2) are differentially required for telomere and centromere cohesion, respectively. REFERENCE 6 (bases 1 to 6186) AUTHORS Prieto,I., Pezzi,N., Buesa,J.M., Kremer,L., Barthelemy,I., Carreiro,C., Roncal,F., Martinez,A., Gomez,L., Fernandez,R., Martinez-A,C. and Barbero,J.L. TITLE STAG2 and Rad21 mammalian mitotic cohesins are implicated in meiosis JOURNAL EMBO Rep. 3 (6), 543-550 (2002) PUBMED 12034751 REFERENCE 7 (bases 1 to 6186) AUTHORS Gregson,H.C., Schmiesing,J.A., Kim,J.S., Kobayashi,T., Zhou,S. and Yokomori,K. TITLE A potential role for human cohesin in mitotic spindle aster assembly JOURNAL J. Biol. Chem. 276 (50), 47575-47582 (2001) PUBMED 11590136 REFERENCE 8 (bases 1 to 6186) AUTHORS Sumara,I., Vorlaufer,E., Gieffers,C., Peters,B.H. and Peters,J.M. TITLE Characterization of vertebrate cohesin complexes and their regulation in prophase JOURNAL J. Cell Biol. 151 (4), 749-762 (2000) PUBMED 11076961 REFERENCE 9 (bases 1 to 6186) AUTHORS Carramolino,L., Lee,B.C., Zaballos,A., Peled,A., Barthelemy,I., Shav-Tal,Y., Prieto,I., Carmi,P., Gothelf,Y., Gonzalez de Buitrago,G., Aracil,M., Marquez,G., Barbero,J.L. and Zipori,D. TITLE SA-1, a nuclear protein encoded by one member of a novel gene family: molecular cloning and detection in hemopoietic organs JOURNAL Gene 195 (2), 151-159 (1997) PUBMED 9305759 REMARK Erratum:[Gene 1998 Jan 12;206(2):283] REFERENCE 10 (bases 1 to 6186) AUTHORS Wu,C., Friedlander,P., Lamoureux,C., Zannis-Hadjopoulos,M. and Price,G.B. TITLE cDNA clones contain autonomous replication activity JOURNAL Biochim. Biophys. Acta 1174 (3), 241-257 (1993) PUBMED 7690594 COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from DA214149.1, CR749433.1, BC001765.1, CB250478.1, BC017095.1 and AA428995.1. Transcript Variant: This variant (2) differs in the 5' UTR compared to variant 1. Variants 1 and 2 encode the same isoform (a). 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 :: CR749433.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025088, ERS025091 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-32 DA214149.1 1-32 33-3223 CR749433.1 2-3192 3224-3780 BC001765.1 3108-3664 3781-4145 CR749433.1 3750-4114 4146-4421 BC001765.1 3919-4194 4422-5038 CB250478.1 34-650 5039-6022 BC017095.1 139-1122 6023-6186 AA428995.1 1-164 c FEATURES Location/Qualifiers source 1..6186 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="X" /map="Xq25" gene 1..6186 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /note="stromal antigen 2" /db_xref="GeneID:10735" /db_xref="HGNC:11355" /db_xref="MIM:300826" exon 1..151 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" exon 152..216 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" variation 161 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="g" /db_xref="dbSNP:181281376" variation 195 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="t" /db_xref="dbSNP:370410456" exon 217..357 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" misc_feature 287..289 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /note="upstream in-frame stop codon" CDS 314..4120 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /note="isoform a is encoded by transcript variant 2; SCC3 homolog 2; cohesin subunit SA-2" /codon_start=1 /product="cohesin subunit SA-2 isoform a" /protein_id="NP_001036215.1" /db_xref="GI:112789528" /db_xref="CCDS:CCDS43990.1" /db_xref="GeneID:10735" /db_xref="HGNC:11355" /db_xref="MIM:300826" /translation="
MIAAPEIPTDFNLLQESETHFSSDTDFEDIEGKNQKQGKGKTCKKGKKGPAEKGKGGNGGGKPPSGPNRMNGHHQQNGVENMMLFEVVKMGKSAMQSVVDDWIESYKHDRDIALLDLINFFIQCSGCKGVVTAEMFRHMQNSEIIRKMTEEFDEDSGDYPLTMAGPQWKKFKSSFCEFIGVLVRQCQYSIIYDEYMMDTVISLLTGLSDSQVRAFRHTSTLAAMKLMTALVNVALNLSINMDNTQRQYEAERNKMIGKRANERLELLLQKRKELQENQDEIENMMNAIFKGVFVHRYRDAIAEIRAICIEEIGIWMKMYSDAFLNDSYLKYVGWTMHDKQGEVRLKCLTALQGLYYNKELNSKLELFTSRFKDRIVSMTLDKEYDVAVQAIKLLTLVLQSSEEVLTAEDCENVYHLVYSAHRPVAVAAGEFLYKKLFSRRDPEEDGMMKRRGRQGPNANLVKTLVFFFLESELHEHAAYLVDSMWDCATELLKDWECMNSLLLEEPLSGEEALTDRQESALIEIMLCTIRQAAECHPPVGRGTGKRVLTAKEKKTQLDDRTKITELFAVALPQLLAKYSVDAEKVTNLLQLPQYFDLEIYTTGRLEKHLDALLRQIRNIVEKHTDTDVLEACSKTYHALCNEEFTIFNRVDISRSQLIDELADKFNRLLEDFLQEGEEPDEDDAYQVLSTLKRITAFHNAHDLSKWDLFACNYKLLKTGIENGDMPEQIVIHALQCTHYVILWQLAKITESSSTKEDLLRLKKQMRVFCQICQHYLTNVNTTVKEQAFTILCDILMIFSHQIMSGGRDMLEPLVYTPDSSLQSELLSFILDHVFIEQDDDNNSADGQQEDEASKIEALHKRRNLLAAFCKLIVYTVVEMNTAADIFKQYMKYYNDYGDIIKETMSKTRQIDKIQCAKTLILSLQQLFNEMIQENGYNFDRSSSTFSGIKELARRFALTFGLDQLKTREAIAMLHKDGIEFAFKEPNPQGESHPPLNLAFLDILSEFSSKLLRQDKRTVYVYLEKFMTFQMSLRREDVWLPLMSYRNSLLAGGDDDTMSVISGISSRGSTVRSKKSKPSTGKRKVVEGMQLSLTEESSSSDSMWLSREQTLHTPVMMQTPQLTSTIMREPKRLRPEDSFMSVYPMQTEHHQTPLDYNTQVTWMLAQRQQEEARQQQERAAMSYVKLRTNLQHAIRRGTSLMEDDEEPIVEDVMMSSEGRIEDLNEGMDFDTMDIDLPPSKNRRERTELKPDFFDPASIMDESVLGVSMF
" misc_feature 773..1093 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /note="STAG domain; Region: STAG; pfam08514" /db_xref="CDD:117091" misc_feature 3494..3496 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /experiment="experimental evidence, no additional details recorded" /note="phosphorylation site" misc_feature 3503..3505 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /experiment="experimental evidence, no additional details recorded" /note="phosphorylation site" misc_feature 3506..3508 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /experiment="experimental evidence, no additional details recorded" /note="phosphorylation site" variation 352 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="g" /db_xref="dbSNP:368486031" exon 358..436 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" variation 371 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="g" /db_xref="dbSNP:188035163" variation 379 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="t" /db_xref="dbSNP:201477761" variation 409 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="g" /db_xref="dbSNP:367889026" exon 437..601 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" exon 602..698 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" variation 648 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="t" /db_xref="dbSNP:140238058" variation 673 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="t" /db_xref="dbSNP:199921026" exon 699..775 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" variation 710 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="g" /db_xref="dbSNP:150057715" variation 721 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="t" /db_xref="dbSNP:145475901" exon 776..980 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" variation 854 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="g" /db_xref="dbSNP:202127296" variation 907 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="t" /db_xref="dbSNP:12838265" exon 981..1132 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" variation 1087 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="g" /db_xref="dbSNP:201520178" variation 1095 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="g" /db_xref="dbSNP:148395642" exon 1133..1206 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" exon 1207..1330 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" exon 1331..1429 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" STS 1352..1484 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /standard_name="REN52332" /db_xref="UniSTS:377132" variation 1357 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="t" /db_xref="dbSNP:193169542" variation 1366 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="g" /db_xref="dbSNP:201201019" variation 1402 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="g" /db_xref="dbSNP:185398645" variation 1414 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="t" /db_xref="dbSNP:190643141" exon 1430..1509 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" variation 1507 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="g" /db_xref="dbSNP:372829731" exon 1510..1617 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" variation 1531 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="t" /db_xref="dbSNP:200552026" variation 1561 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="g" /db_xref="dbSNP:142571900" exon 1618..1729 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" variation 1655 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="g" /db_xref="dbSNP:146439650" variation 1672 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="g" /db_xref="dbSNP:370465019" exon 1730..1847 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" variation 1762 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="t" /db_xref="dbSNP:140900528" variation 1823 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="g" /replace="t" /db_xref="dbSNP:180841941" exon 1848..1951 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" variation 1864 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="g" /db_xref="dbSNP:201565008" variation 1883 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="g" /db_xref="dbSNP:144820719" variation 1902 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="g" /db_xref="dbSNP:5911741" variation 1942 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="g" /db_xref="dbSNP:202037021" exon 1952..2044 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" exon 2045..2134 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" variation 2047 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="g" /db_xref="dbSNP:146721074" exon 2135..2338 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" variation 2313 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="g" /db_xref="dbSNP:369728409" variation 2318 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="c" /db_xref="dbSNP:140406522" variation 2330 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="t" /db_xref="dbSNP:184717615" exon 2339..2409 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" variation 2356 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="g" /db_xref="dbSNP:371293594" variation 2395 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="t" /db_xref="dbSNP:10217943" exon 2410..2497 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" variation 2410 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="g" /replace="t" /db_xref="dbSNP:6655782" variation 2419 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="t" /db_xref="dbSNP:373076947" variation 2451 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="t" /db_xref="dbSNP:112417641" variation 2489 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="t" /db_xref="dbSNP:138155911" exon 2498..2578 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" exon 2579..2671 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" exon 2672..2846 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" variation 2694 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="t" /db_xref="dbSNP:149551481" exon 2847..2986 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" variation 2911 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="t" /db_xref="dbSNP:201474861" variation 2914 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="g" /db_xref="dbSNP:374308808" variation 2971 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="t" /db_xref="dbSNP:368522338" exon 2987..3088 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" variation 2998 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="t" /db_xref="dbSNP:200047549" exon 3089..3237 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" variation 3142 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="t" /db_xref="dbSNP:202140215" exon 3238..3366 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" variation 3337 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="t" /db_xref="dbSNP:368960276" exon 3367..3590 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" variation 3404 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="t" /db_xref="dbSNP:370347095" variation 3491 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="g" /db_xref="dbSNP:146561651" variation 3519 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="t" /db_xref="dbSNP:11555621" variation 3544 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="g" /db_xref="dbSNP:139192022" variation 3545 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="t" /db_xref="dbSNP:373076855" exon 3591..3780 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" variation 3673 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="t" /db_xref="dbSNP:34567090" variation 3678 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="t" /db_xref="dbSNP:370975120" variation 3700 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="g" /db_xref="dbSNP:374627302" variation 3714 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="t" /db_xref="dbSNP:5911751" variation 3743 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="g" /db_xref="dbSNP:147520054" exon 3781..3891 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" variation 3788..3789 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="" /replace="g" /db_xref="dbSNP:35494370" variation 3796 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="g" /replace="t" /db_xref="dbSNP:193279915" variation 3830 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="g" /db_xref="dbSNP:367702969" exon 3892..4018 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" variation 3982 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="t" /db_xref="dbSNP:372132155" variation 4004 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="g" /db_xref="dbSNP:182467825" exon 4019..4096 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" variation 4093 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="t" /db_xref="dbSNP:201262699" exon 4097..6179 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /inference="alignment:Splign:1.39.8" variation 4159 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="t" /db_xref="dbSNP:377029295" STS 4163..4398 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /standard_name="REN52548" /db_xref="UniSTS:377348" variation 4170 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="g" /db_xref="dbSNP:369223493" variation 4207 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="t" /db_xref="dbSNP:111649101" variation 4208 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="g" /db_xref="dbSNP:186381656" STS 4262..5419 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /standard_name="stSG633685" /db_xref="UniSTS:460325" variation 4367..4370 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="" /replace="gtta" /db_xref="dbSNP:368531652" STS 4375..4635 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /standard_name="REN52549" /db_xref="UniSTS:377349" variation 4407 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="" /replace="a" /db_xref="dbSNP:67492414" variation 4415 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="c" /db_xref="dbSNP:113412506" STS 4430..4985 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /standard_name="ECD12003" /db_xref="UniSTS:293036" STS 4612..4839 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /standard_name="REN52550" /db_xref="UniSTS:377350" variation 4694 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="g" /db_xref="dbSNP:144559029" STS 4781..5044 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /standard_name="REN52551" /db_xref="UniSTS:377351" STS 5029..5281 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /standard_name="REN52552" /db_xref="UniSTS:377352" variation 5044 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="g" /replace="t" /db_xref="dbSNP:183029659" variation 5063 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="t" /db_xref="dbSNP:1044020" STS 5206..5791 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /standard_name="ECD10983" /db_xref="UniSTS:292020" STS 5241..5502 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /standard_name="REN52553" /db_xref="UniSTS:377353" variation 5260 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="t" /db_xref="dbSNP:187706335" variation 5473..5476 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="" /replace="ctat" /db_xref="dbSNP:72013495" STS 5479..5718 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /standard_name="REN52554" /db_xref="UniSTS:377354" variation 5638 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="g" /db_xref="dbSNP:192624442" STS 5694..5946 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /standard_name="REN52555" /db_xref="UniSTS:377355" STS 5773..6003 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /standard_name="DXS8321" /db_xref="UniSTS:77560" variation 5901..5902 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="" /replace="aa" /db_xref="dbSNP:71761944" polyA_signal 6002..6007 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" polyA_signal 6008..6013 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" polyA_site 6020 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" variation 6043 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="g" /db_xref="dbSNP:377387979" variation 6052 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="a" /replace="g" /db_xref="dbSNP:370425648" variation 6073 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" /replace="c" /replace="t" /db_xref="dbSNP:183365442" polyA_signal 6153..6158 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" polyA_site 6179 /gene="STAG2" /gene_synonym="bA517O1.1; SA-2; SA2; SCC3B" ORIGIN
ctctcttcctcccttcctagagagggaacaacattcatgtgacgggcccctctgcttctcccccgccccatcatctccagcgcgtggtgggggaactgctggggaaggcgattggcatcgatctctccatcccttccgaggcccgacttcggtggccaccgagtactaaattcacttgggaataaaagaaaaacataagaaaattataagagaaaggaattgtcttagaagaaagaaggcaagccaccattttacccacgtaaatatatgaatatatttctgacattgaggtgttccagaagatgataaagaaatgatagcagctccagaaataccaactgattttaatctactacaggagtcagaaacacatttttcttctgacacagattttgaagatatcgaaggaaaaaaccaaaagcaaggcaaaggcaaaacttgtaaaaaaggcaaaaagggcccagcagaaaagggcaaaggtggaaatggaggaggaaaacctccttctggtccaaaccgaatgaatggtcatcaccaacagaatggagtggaaaacatgatgttgtttgaagttgttaaaatgggcaagagtgctatgcagtcggtggtagatgattggatagaatcatacaagcatgaccgagatatagcacttcttgaccttatcaacttttttattcagtgttcaggctgtaaaggagttgtcacagcagaaatgtttagacatatgcagaactctgagataattcgaaaaatgactgaagaattcgatgaggatagtggagattatccacttaccatggctggtcctcagtggaagaagttcaaatccagtttttgtgaattcattggcgtgttagtacggcaatgtcaatatagtatcatatatgatgagtatatgatggatacagtcatttcacttcttacaggattgtctgactcacaagtcagagcatttcgacatacaagcaccctggcagctatgaagttgatgacagctttggtgaatgtggcactaaatcttagcattaatatggataatacacaaagacaatatgaagcagaacggaataaaatgattggaaaacgagccaatgagaggctagaactcctgctacaaaagcggaaagagcttcaggaaaatcaagatgaaatagaaaatatgatgaatgcaatatttaaaggagtgtttgtacatagataccgtgatgcgatagctgaaattcgagctatttgcattgaagagattggcatttggatgaagatgtatagtgatgcctttcttaatgacagttatttaaaatatgttggttggactatgcatgataagcaaggtgaagtaagactcaaatgtcttactgctctacaagggctttattataacaaagagcttaattccaaactggaactttttaccagtcggttcaaggatagaattgtgtctatgacccttgacaaagaatatgatgttgcagtacaagcaataaaattactcactcttgttttacagagtagtgaagaagttctcactgcagaagattgtgaaaatgtctatcatctggtttattcagctcaccggccagtagcagtagcagctggagaatttctctacaaaaagctcttcagtcgtagagatccagaggaggatggaatgatgaaaagaagaggaagacaaggtccaaatgccaaccttgttaagacattggtttttttctttctagaaagtgagttacatgagcatgcagcataccttgtggatagcatgtgggactgtgctactgagctgctgaaagactgggaatgtatgaatagcttgttactggaagagccacttagtggagaggaagcactaacagataggcaagagagtgctctgattgaaataatgctttgtaccattagacaagcggctgaatgtcatcctcccgtgggaagagggacaggaaaaagggtgcttacagcaaaggagaagaagacacagttggatgataggacaaaaatcactgagctttttgccgtggcccttcctcagttattagcaaaatactctgtagatgcagaaaaggtgactaacttgttgcagttgcctcagtactttgatttggaaatatataccactggacgattagaaaagcatttggatgccttattgcgacagatccggaatattgtagagaagcacacagatacagatgttttggaagcatgttctaaaacttaccatgcactctgtaatgaagagttcacaatcttcaacagagtagatatttcaagaagtcaactgatagatgaattggcagataaatttaaccggcttcttgaagattttctgcaagagggtgaagaacctgatgaagatgatgcatatcaggtattgtcaacattgaagaggatcactgcttttcataatgcccatgacctttcaaagtgggatttatttgcttgtaattacaaactcttgaaaactggaatcgaaaatggagacatgcctgagcagattgttattcacgcactgcagtgtactcactatgtaatcctttggcaacttgctaagataactgaaagcagctctacaaaggaggacttgctgcgtttaaagaaacaaatgagagtattttgtcagatatgtcaacattacctgaccaacgtgaatactactgttaaggaacaggccttcactattctgtgtgatattttgatgatcttcagccatcagattatgtcaggagggcgtgacatgttagagccattagtgtatacccctgattcttcattgcagtctgagttgctcagctttattttggatcatgtcttcattgaacaggatgatgataataatagtgcagatggtcagcaagaggatgaagccagtaaaattgaagctctgcacaagagaagaaatttacttgcagcattttgtaagctaattgtatatactgtggtggagatgaatacagctgcagatatcttcaaacagtatatgaagtattataatgactatggagatatcatcaaagaaacaatgagtaaaacaaggcagatagacaaaattcagtgtgctaagacccttattctcagtctgcaacagctttttaatgaaatgatacaagaaaatggctataattttgatagatcatcctctacatttagtggcataaaagaacttgctcgacgttttgctttaacttttggacttgatcagttgaaaacaagagaagccattgccatgctacacaaagatggcatagaatttgcttttaaagagcctaatccgcaaggggagagccatccacctttaaatttggcatttcttgatattctgagtgaattttcttctaaactacttcgacaagacaaaagaacagtgtatgtttacttggaaaagttcatgacctttcagatgtcactccgaagagaggatgtgtggcttccactgatgtcttaccgaaattctttgctagctggtggtgatgatgacaccatgtcagtcattagtggaatcagcagccgggggtcaacagtacggagtaaaaaatcaaaaccatctacaggaaaacggaaagtggttgagggcatgcagctttcactcactgaagaaagtagtagtagtgacagtatgtggttaagcagagaacaaacactgcacacccctgttatgatgcagacaccacaactcacctccactattatgagagagcccaaaagattacggcctgaggatagcttcatgagtgtttatccaatgcagactgaacatcatcaaacacctcttgattataacacgcaggtaacatggatgttagctcaaagacaacaagaggaagcaaggcaacagcaggagagagcagcaatgagctatgttaaactgcgaactaatcttcagcatgccattcggcgtggcacaagcctaatggaagatgatgaagagccaattgtggaagatgttatgatgtcctcagaagggaggattgaggatcttaatgagggaatggattttgacaccatggatatagatttgccaccatcaaagaacagacgagagagaacagaactgaagcctgatttctttgatccagcttcaattatggatgaatcagttcttggagtgtcaatgttttaataccagtacacaattaaatctgtggtgaagtcattttctaagtggaagaggaaattttaaagtgtggtagatacagtgaaattctgtacagatttttctctaaggagaatatgacatgcttatgcttaccaagatcaagtgcattgaggggcagttttgtttgcctgaataaacgtaaaggacaagtaaacaatttgatgataagctacagtttttcttagaaagtaaatattttatttatgcgctgttagttggcttttgaatcgattatttcatgcttttttttaaaaaaaaaaaaaaacaaaataacaatctgaagaggcatttggtacagatatgaattctcttacatttatttactggttgtactaaataatgatgacctctgctggatttctgtttacatccagaaaacaatgttaaggatgtatttattcccctaccctgaagaaagtgtaggatagaattgtttttagcattctaaatttaaatgcttaaaacgtcaatcaacaaaactttgttttaaatattgtaattgtggagaaaagtaaacttataagcagaacttttacaattttttcatctaaaagtattttaagatatttttaaaatccaagagcttctctatacttttcagaaatatccagatgcagtgaactgccagaaggtaaccagtctcaaacatgcttatcccattatcaaccctgaaagtttgcttgtcctttaagataaaaatgtaatgttgtgatattccttccagtaatgccactgtattttgtctccaaataaaagaagcttattgtagtatgtttgcagaaaaattctaaacaaaaattatacagcttattagagtgtgggaatagggatctaaattttaaataaaattatatatatatataaattggtgctgattttataattgcgcagtttgtttagttttttcttacttttaaattccaacttaaaattatgaggtttcagaaatatattgaaagtttaacaatgtttaaaaatagaaaagcatgagtgttcatgctttaaaatgatttttaaatttgtattttatattgttttatctatctgtctttgcaagcagtcttcaggttaaagatacttctaacaggttacagtacatttcctctgtatgtaaattagatgggataatagaattcataacccataatattctttgaaagctaagctttaaacttcattttatgtcctttcacaaataaattagtttaaaacagaaagtggctacttgccattttgacatcaactcattttgcgaggcttaggcagctagacatcgtttaaaacaaaatattaacttatattacatgtgtatctatctattgtcagtcgtctctcagttcttgaggtatattattttaatcattccatgccttaatatgcttgcaatacaagaatatcttcagatgggtgaataccaaaaggctttcagtttttagtcagaaatcaagcattgggctgtggtagccaaaaaccataggttagctaaaaagatcatgatacaattattttattaagtcatggttaataacaaatgaatccagacttgtctaacagattttccatcaacaaatattgttatgtgcaaaagtattgcctatgttgttttacacaccactgcattaactagaactgctgagaggactgtatatatgattttaaacctaagttgattttttttctcactcttgaaaggagtacttctttgtgaaagcagttcttacagctttgttttcaaccagctaaaaatgttttatatattactctaacctgttgtcctccacattctattgtcctaattgtactgttttctgatttgtatttatgtcttgagacagtaactttttgaataaaaataaacctacagtatgttgtatgttttctcttgtactcaaagggggagggtggctataaatggtttgcaaatttatatctattatcacatcttttaatgtgtttggggaataatttatagagaataccatcagtttatatttttaataaatcatatgtatttacaatgaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:10735 -> Molecular function: GO:0005515 [protein binding] evidence: IPI GeneID:10735 -> Biological process: GO:0000278 [mitotic cell cycle] evidence: TAS GeneID:10735 -> Biological process: GO:0000910 [cytokinesis] evidence: TAS GeneID:10735 -> Biological process: GO:0007062 [sister chromatid cohesion] evidence: IMP GeneID:10735 -> Biological process: GO:0007067 [mitosis] evidence: IEA GeneID:10735 -> Biological process: GO:0007126 [meiosis] evidence: IEA GeneID:10735 -> Biological process: GO:0019827 [stem cell maintenance] evidence: IEA GeneID:10735 -> Biological process: GO:0032876 [negative regulation of DNA endoreduplication] evidence: IMP GeneID:10735 -> Cellular component: GO:0000775 [chromosome, centromeric region] evidence: TAS GeneID:10735 -> Cellular component: GO:0000785 [chromatin] evidence: IDA GeneID:10735 -> Cellular component: GO:0005634 [nucleus] evidence: TAS GeneID:10735 -> Cellular component: GO:0005654 [nucleoplasm] evidence: TAS GeneID:10735 -> Cellular component: GO:0005694 [chromosome] evidence: TAS GeneID:10735 -> Cellular component: GO:0005829 [cytosol] evidence: TAS
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