2025-05-09 19:25:55, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_007252 2324 bp mRNA linear PRI 15-JUN-2013 DEFINITION Homo sapiens POU class 6 homeobox 2 (POU6F2), transcript variant 1, mRNA. ACCESSION NM_007252 VERSION NM_007252.3 GI:260436856 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 2324) 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 2 (bases 1 to 2324) AUTHORS Anney,R., Klei,L., Pinto,D., Regan,R., Conroy,J., Magalhaes,T.R., Correia,C., Abrahams,B.S., Sykes,N., Pagnamenta,A.T., Almeida,J., Bacchelli,E., Bailey,A.J., Baird,G., Battaglia,A., Berney,T., Bolshakova,N., Bolte,S., Bolton,P.F., Bourgeron,T., Brennan,S., Brian,J., Carson,A.R., Casallo,G., Casey,J., Chu,S.H., Cochrane,L., Corsello,C., Crawford,E.L., Crossett,A., Dawson,G., de Jonge,M., Delorme,R., Drmic,I., Duketis,E., Duque,F., Estes,A., Farrar,P., Fernandez,B.A., Folstein,S.E., Fombonne,E., Freitag,C.M., Gilbert,J., Gillberg,C., Glessner,J.T., Goldberg,J., Green,J., Guter,S.J., Hakonarson,H., Heron,E.A., Hill,M., Holt,R., Howe,J.L., Hughes,G., Hus,V., Igliozzi,R., Kim,C., Klauck,S.M., Kolevzon,A., Korvatska,O., Kustanovich,V., Lajonchere,C.M., Lamb,J.A., Laskawiec,M., Leboyer,M., Le Couteur,A., Leventhal,B.L., Lionel,A.C., Liu,X.Q., Lord,C., Lotspeich,L., Lund,S.C., Maestrini,E., Mahoney,W., Mantoulan,C., Marshall,C.R., McConachie,H., McDougle,C.J., McGrath,J., McMahon,W.M., Melhem,N.M., Merikangas,A., Migita,O., Minshew,N.J., Mirza,G.K., Munson,J., Nelson,S.F., Noakes,C., Noor,A., Nygren,G., Oliveira,G., Papanikolaou,K., Parr,J.R., Parrini,B., Paton,T., Pickles,A., Piven,J., Posey,D.J., Poustka,A., Poustka,F., Prasad,A., Ragoussis,J., Renshaw,K., Rickaby,J., Roberts,W., Roeder,K., Roge,B., Rutter,M.L., Bierut,L.J., Rice,J.P., Salt,J., Sansom,K., Sato,D., Segurado,R., Senman,L., Shah,N., Sheffield,V.C., Soorya,L., Sousa,I., Stoppioni,V., Strawbridge,C., Tancredi,R., Tansey,K., Thiruvahindrapduram,B., Thompson,A.P., Thomson,S., Tryfon,A., Tsiantis,J., Van Engeland,H., Vincent,J.B., Volkmar,F., Wallace,S., Wang,K., Wang,Z., Wassink,T.H., Wing,K., Wittemeyer,K., Wood,S., Yaspan,B.L., Zurawiecki,D., Zwaigenbaum,L., Betancur,C., Buxbaum,J.D., Cantor,R.M., Cook,E.H., Coon,H., Cuccaro,M.L., Gallagher,L., Geschwind,D.H., Gill,M., Haines,J.L., Miller,J., Monaco,A.P., Nurnberger,J.I. Jr., Paterson,A.D., Pericak-Vance,M.A., Schellenberg,G.D., Scherer,S.W., Sutcliffe,J.S., Szatmari,P., Vicente,A.M., Vieland,V.J., Wijsman,E.M., Devlin,B., Ennis,S. and Hallmayer,J. TITLE A genome-wide scan for common alleles affecting risk for autism JOURNAL Hum. Mol. Genet. 19 (20), 4072-4082 (2010) PUBMED 20663923 REMARK GeneRIF: Observational study and genome-wide association study of gene-disease association. (HuGE Navigator) REFERENCE 3 (bases 1 to 2324) AUTHORS Joslyn,G., Ravindranathan,A., Brush,G., Schuckit,M. and White,R.L. TITLE Human variation in alcohol response is influenced by variation in neuronal signaling genes JOURNAL Alcohol. Clin. Exp. Res. 34 (5), 800-812 (2010) PUBMED 20201926 REMARK GeneRIF: Observational study and genome-wide association study of gene-disease association. (HuGE Navigator) REFERENCE 4 (bases 1 to 2324) AUTHORS Di Renzo,F., Doneda,L., Menegola,E., Sardella,M., De Vecchi,G., Collini,P., Spreafico,F., Fossati-Bellani,F., Giavini,E., Radice,P. and Perotti,D. TITLE The murine Pou6f2 gene is temporally and spatially regulated during kidney embryogenesis and its human homolog is overexpressed in a subset of Wilms tumors JOURNAL J. Pediatr. Hematol. Oncol. 28 (12), 791-797 (2006) PUBMED 17164647 REFERENCE 5 (bases 1 to 2324) AUTHORS Perotti,D., Vecchi,G.D., Lualdi,E., Testi,M.A., Sozzi,G., Collini,P., Spreafico,F., Terenziani,M., Fossati-Bellani,F. and Radice,P. TITLE Wilms tumor in monozygous twins: clinical, pathological, cytogenetic and molecular case report JOURNAL J. Pediatr. Hematol. Oncol. 27 (10), 521-525 (2005) PUBMED 16217254 REFERENCE 6 (bases 1 to 2324) AUTHORS Perotti,D., De Vecchi,G., Testi,M.A., Lualdi,E., Modena,P., Mondini,P., Ravagnani,F., Collini,P., Di Renzo,F., Spreafico,F., Terenziani,M., Sozzi,G., Fossati-Bellani,F. and Radice,P. TITLE Germline mutations of the POU6F2 gene in Wilms tumors with loss of heterozygosity on chromosome 7p14 JOURNAL Hum. Mutat. 24 (5), 400-407 (2004) PUBMED 15459955 REMARK GeneRIF: observations suggest that POU6F2 is a tumor suppressor and is involved in hereditary predisposition to Wilms tumor REFERENCE 7 (bases 1 to 2324) AUTHORS Perotti,D., Testi,M.A., Mondini,P., Pilotti,S., Green,E.D., Pession,A., Sozzi,G., Pierotti,M.A., Fossati-Bellani,F. and Radice,P. TITLE Refinement within single yeast artificial chromosome clones of a minimal region commonly deleted on the short arm of chromosome 7 in Wilms tumours JOURNAL Genes Chromosomes Cancer 31 (1), 42-47 (2001) PUBMED 11284034 REFERENCE 8 (bases 1 to 2324) AUTHORS Phillips,K. and Luisi,B. TITLE The virtuoso of versatility: POU proteins that flex to fit JOURNAL J. Mol. Biol. 302 (5), 1023-1039 (2000) PUBMED 11183772 REMARK Review article REFERENCE 9 (bases 1 to 2324) AUTHORS Zhou,H., Yoshioka,T. and Nathans,J. TITLE Retina-derived POU-domain factor-1: a complex POU-domain gene implicated in the development of retinal ganglion and amacrine cells JOURNAL J. Neurosci. 16 (7), 2261-2274 (1996) PUBMED 8601806 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from DN991890.1, U91935.1 and AC005483.1. This sequence is a reference standard in the RefSeqGene project. On Oct 3, 2009 this sequence version replaced gi:51873039. Summary: This gene encodes a member of the POU protein family characterized by the presence of a bipartite DNA binding domain, consisting of a POU-specific domain and a homeodomain, separated by a variable polylinker. The DNA binding domain may bind to DNA as monomers or as homo- and/or heterodimers, in a sequence-specific manner. The POU family members are transcriptional regulators, many of which are known to control cell type-specific differentiation pathways. This gene is a tumor suppressor involved in Wilms tumor (WT) predisposition. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.[provided by RefSeq, Oct 2009]. Transcript Variant: This variant (1) is the longer transcript and encodes the longer isoform (1). Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-107 DN991890.1 19-125 108-732 U91935.1 48-672 733-1028 AC005483.1 150160-150455 c 1029-1201 U91935.1 972-1144 1202-1376 AC005483.1 56892-57066 c 1377-1714 U91935.1 1320-1657 1715-2324 AC005483.1 25384-25993 c FEATURES Location/Qualifiers source 1..2324 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="7" /map="7p14.1" gene 1..2324 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /note="POU class 6 homeobox 2" /db_xref="GeneID:11281" /db_xref="HGNC:21694" /db_xref="MIM:609062" exon 1..50 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /inference="alignment:Splign:1.39.8" variation 38 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="t" /db_xref="dbSNP:191832829" exon 51..161 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /inference="alignment:Splign:1.39.8" variation 111 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="c" /db_xref="dbSNP:371792908" misc_feature 123..125 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /note="upstream in-frame stop codon" variation 131 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:199780108" variation 137 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:370067576" CDS 144..2219 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /note="isoform 1 is encoded by transcript variant 1; Wilms tumor suppressor locus; POU domain, class 6, transcription factor 2; retina-derived POU-domain factor-1; retina-derived POU domain factor 1" /codon_start=1 /product="POU domain, class 6, transcription factor 2 isoform 1" /protein_id="NP_009183.3" /db_xref="GI:157743257" /db_xref="CCDS:CCDS34620.2" /db_xref="GeneID:11281" /db_xref="HGNC:21694" /db_xref="MIM:609062" /translation="
MSALLQDPMIAGQVSKPLLSVRSEMNAELRGEDKAATSDSELNEPLLAPVESNDSEDTPSKLFGARGNPALSDPGTPDQHQASQTHPPFPVGPQPLLTAQQLASAVAGVMPGGPPALNQPILIPFNMAGQLGGQQGLVLTLPTANLTNIQGLVAAAAAGGIMTLPLQNLQATSSLNSQLQQLQLQLQQQQQQQQQQPPPSTNQHPQPAPQAPSQSQQQPLQPTPPQQPPPASQQPPAPTSQLQQAPQPQQHQPHSHSQNQNQPSPTQQSSSPPQKPSQSPGHGLPSPLTPPNPLQLVNNPLASQAAAAAAAMSSIASSQAFGNALSSLQGVTGQLVTNAQGQIIGTIPLMPNPGPSSQAASGTQGLQVQPITPQLLTNAQGQIIATVIGNQILPVINTQGITLSPIKPGQQLHQPSQTSVGQAASQGNLLHLAHSQASMSQSPVRQASSSSSSSSSSSALSVGQLVSNPQTAAGEVDGVNLEEIREFAKAFKIRRLSLGLTQTQVGQALSATEGPAYSQSAICRHTILRSHFFLPQEAQENTIASSLTAKLNPGLLYPARFEKLDITPKSAQKIKPVLERWMAEAEARHRAGMQNLTEFIGSEPSKKRKRRTSFTPQALEILNAHFEKNTHPSGQEMTEIAEKLNYDREVVRVWFCNKRQALKNTIKRLKQHEPATAVPLEPLTDSLEENS
" misc_feature 1572..1901 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /note="Pou domain - N-terminal to homeobox domain; Region: Pou; cl02582" /db_xref="CDD:198730" misc_feature 1965..2138 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /note="Homeodomain; DNA binding domains involved in the transcriptional regulation of key eukaryotic developmental processes; may bind to DNA as monomers or as homo- and/or heterodimers, in a sequence-specific manner; Region: homeodomain; cd00086" /db_xref="CDD:28970" misc_feature order(1965..1979,1983..1985,2034..2036,2052..2054, 2091..2093,2097..2102,2109..2114,2118..2126,2130..2135) /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /note="DNA binding site [nucleotide binding]" /db_xref="CDD:28970" misc_feature order(1971..1973,1980..1982,2100..2102,2109..2114, 2121..2123) /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /note="specific DNA base contacts [nucleotide binding]; other site" /db_xref="CDD:28970" exon 162..333 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /inference="alignment:Splign:1.39.8" variation 168 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:144817326" variation 217 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="t" /db_xref="dbSNP:199673767" variation 221 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:145866494" variation 224 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="g" /db_xref="dbSNP:376754165" variation 225 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="g" /replace="t" /db_xref="dbSNP:369976707" variation 259 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="t" /db_xref="dbSNP:148998895" variation 262 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="g" /replace="t" /db_xref="dbSNP:373529275" variation 308 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:192309744" variation 326 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="g" /db_xref="dbSNP:371496157" variation 333 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:199858565" exon 334..425 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /inference="alignment:Splign:1.39.8" variation 364 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:373840004" variation 365 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="c" /db_xref="dbSNP:199994299" variation 404 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="g" /db_xref="dbSNP:143669624" variation 406 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:201880507" variation 411 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:148094915" variation 419 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="g" /replace="t" /db_xref="dbSNP:141204834" exon 426..654 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /inference="alignment:Splign:1.39.8" variation 458 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:145078077" variation 460 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:138865854" variation 491 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:142566948" variation 509 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:138654387" variation 559 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="g" /replace="t" /db_xref="dbSNP:368561673" variation 575 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:143731302" variation 587 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:139491714" variation 588 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="t" /db_xref="dbSNP:143406388" exon 655..1028 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /inference="alignment:Splign:1.39.8" variation 671 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:147178262" variation 699 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:140348812" variation 706 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="t" /db_xref="dbSNP:201163431" variation 707 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="g" /db_xref="dbSNP:201782254" variation 716 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="g" /replace="t" /db_xref="dbSNP:121918261" variation 723 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="c" /db_xref="dbSNP:183758448" variation 739 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:2074936" variation 748 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:151293651" variation 845 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="g" /replace="t" /db_xref="dbSNP:80127606" variation 877 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:150071017" variation 878 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="g" /replace="t" /db_xref="dbSNP:145403612" variation 899..900 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="" /replace="c" /db_xref="dbSNP:35091229" variation 900 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:373709968" variation 910 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:373622114" variation 947 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:200308619" variation 960 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="c" /db_xref="dbSNP:367834526" variation 961 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:144939808" variation 962 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:202064223" variation 982 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:146819544" variation 1003 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:140579551" variation 1012 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:201672868" variation 1025 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:368361923" exon 1029..1169 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /inference="alignment:Splign:1.39.8" variation 1064 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:148254024" variation 1077 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:376654925" variation 1079 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:141249466" variation 1133 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:150386704" variation 1153 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="g" /db_xref="dbSNP:200602029" exon 1170..1376 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /inference="alignment:Splign:1.39.8" variation 1175 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:2302124" variation 1202 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:2302123" variation 1210 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="c" /db_xref="dbSNP:373122380" variation 1211 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:147128853" variation 1226 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:368929654" variation 1233 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:140425700" variation 1238 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="c" /db_xref="dbSNP:373309283" variation 1277 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:149279532" variation 1283 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:144488464" variation 1292 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="c" /db_xref="dbSNP:148571075" variation 1317 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:376392988" variation 1325 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:201471567" variation 1326 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:376245818" variation 1340 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:2302122" variation 1348 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="g" /db_xref="dbSNP:146637189" variation 1368 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:140161191" variation 1370 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="g" /db_xref="dbSNP:143607091" variation 1376 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:191138577" exon 1377..1545 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /inference="alignment:Splign:1.39.8" variation 1396 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:374384343" variation 1403 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:146778737" variation 1426 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="c" /db_xref="dbSNP:75367520" variation 1443 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:367970454" variation 1459 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:372113314" variation 1463 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="g" /replace="t" /db_xref="dbSNP:375493176" variation 1471 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:202234462" variation 1483 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="g" /db_xref="dbSNP:140486504" variation 1495 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:368375577" variation 1505 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:150437987" variation 1527 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:372667357" exon 1546..1714 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /inference="alignment:Splign:1.39.8" variation 1556 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:371316682" variation 1578 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="g" /db_xref="dbSNP:375867583" variation 1596 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="g" /db_xref="dbSNP:145241880" variation 1626 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:368700023" variation 1641 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="c" /db_xref="dbSNP:4992268" variation 1663 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:200235640" variation 1684 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:369179055" variation 1702 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:199649027" exon 1715..2324 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /inference="alignment:Splign:1.39.8" variation 1736 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:373469942" variation 1764 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:201323897" variation 1779 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="t" /db_xref="dbSNP:148888580" variation 1811 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:143525120" variation 1869 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:201812532" variation 1881 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:369610763" variation 1905 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:138208739" variation 1931 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="g" /db_xref="dbSNP:200692209" variation 1934 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:143694290" variation 1935 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:146116211" variation 1955 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="c" /db_xref="dbSNP:373380693" variation 1975 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:200415799" STS 2026..2194 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /standard_name="RH71269" /db_xref="UniSTS:11260" variation 2028 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="c" /db_xref="dbSNP:145961110" variation 2057 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="g" /db_xref="dbSNP:371560771" variation 2058 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:7804851" variation 2085 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:373556433" variation 2086 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:201519589" variation 2094 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:377002404" variation 2145 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:150758284" variation 2164 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="c" /db_xref="dbSNP:137959267" variation 2169 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="c" /db_xref="dbSNP:149617494" variation 2170 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:372919598" variation 2171 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="g" /replace="t" /db_xref="dbSNP:146111946" variation 2207 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="g" /db_xref="dbSNP:140193353" variation 2224 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="c" /db_xref="dbSNP:373654083" variation 2231 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="c" /replace="t" /db_xref="dbSNP:376847927" variation 2258 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="a" /replace="c" /db_xref="dbSNP:367793536" variation 2261 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="g" /replace="t" /db_xref="dbSNP:138603140" variation 2283..2285 /gene="POU6F2" /gene_synonym="RPF-1; WT5; WTSL" /replace="" /replace="aca" /db_xref="dbSNP:201268962" ORIGIN
atctctcagcgcagcaggacacggggaccatgcaagctgtaattggtcaggcatgaactctcttgggttgtgttaccctgtttgctgtttactgtcaagatgctgaaagaatgttcttataatgatccaagaggaagtggcaaatgagtgctcttcttcaggatccaatgatagctggacaagtcagtaagcccttgctgtcagtgcggagtgaaatgaatgcggagttgagaggtgaggacaaggctgctacttcagacagcgagctgaatgagcccctgcttgcgcctgtggaatcaaatgacagcgaggacactcccagcaagctcttcggggctagaggaaacccagcattatcagacccaggcactcctgaccaacaccaggccagtcagacccaccccccatttccagttgggccacagccacttctgacggcacagcagttagcttctgctgtggccggcgtgatgccgggaggccccccagccctcaaccagccaatcctcattcccttcaacatggcgggacagctaggaggccagcaaggactggttctcacactgccaacagcgaatctcaccaacatccaagggctggtggcagcagctgcagccggaggcattatgactctgccactgcaaaatctacaagctacctcatccctgaactcccagctccagcagctccagctccagctccagcagcagcagcagcagcagcagcagcagcctcccccgtcaaccaaccagcacccgcaaccagccccacaggcgccctcgcagtcccagcagcagccgctgcagcccaccccaccccagcagccaccacccgcctctcagcagccgccagctcctacatctcagctgcaacaggcgcctcagccccagcagcaccaaccccactcccactcccagaaccagaaccaaccatctccaacccagcagagctccagccccccgcagaaacctagtcagtctccaggacatggcctgccttcaccgctcacgccacccaatcctctacagctggttaataatccactagcaagtcaggctgcagcggctgcagcagccatgagctccatagcaagctcacaggcctttggcaatgccctctccagtcttcagggggtcacaggtcaactagttactaatgcacaaggacagattatcgggaccattccactgatgcctaatccagggccatcgagccaagcagcaagcggcactcagggcttgcaagtgcagccaatcaccccccagctcctcacaaacgcccagggccagatcatcgccacagtcattgggaaccagatcctgcccgtgatcaacacccagggcatcacgctgtcacccatcaagcccggccagcagctccaccaaccctcccagacgtcagtgggtcaagcagcctcccaaggcaaccttctgcacctggctcacagccaagcatccatgtctcaaagtcccgtccggcaggcttcctcttcttcctcctcatcctcctcttcttcagctttgagcgtgggccagttagtcagcaatcctcaaacggcagcgggtgaggtggatggggttaatctggaggagatccgagaatttgccaaagcttttaaaatccggcgcctgtcccttggcctgacccagactcaggtgggacaggctctcagtgctacagagggccccgcgtacagccagtcggccatctgcagacacaccatcctgagaagccactttttcctaccacaggaagcccaagagaacactatagctagcagtctgacagccaaactgaaccctggccttttgtatcctgccaggtttgaaaagctggacatcacccctaaaagtgcccagaagatcaagccggtgcttgagcggtggatggctgaggctgaggcccgccatcgagcaggtatgcagaacctgaccgagtttatcgggagtgaaccatccaaaaagcgcaagcggcgcacctccttcacaccccaggcccttgagatcctcaatgcccactttgagaagaacacacacccttctgggcaggaaatgaccgaaattgctgagaagctgaactatgaccgagaagtagttagagtttggttctgcaataagaggcaagccctgaagaacacaattaaacgcttaaaacagcacgagccggccacggcagtccctttggagcccttaacagactctctggaagaaaactcctaaagagatgcccacccataatcagaagcaaaattcacagaaactaaactccacccttgggactccacaacaacaacaacaacaaaatttaatttaatttaaaaatag
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:11281 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: TAS GeneID:11281 -> Molecular function: GO:0043565 [sequence-specific DNA binding] evidence: IEA GeneID:11281 -> Biological process: GO:0006355 [regulation of transcription, DNA-dependent] evidence: TAS GeneID:11281 -> Biological process: GO:0006366 [transcription from RNA polymerase II promoter] evidence: TAS GeneID:11281 -> Biological process: GO:0007402 [ganglion mother cell fate determination] evidence: TAS GeneID:11281 -> Biological process: GO:0007417 [central nervous system development] evidence: TAS GeneID:11281 -> Biological process: GO:0007601 [visual perception] evidence: TAS GeneID:11281 -> Cellular component: GO:0005634 [nucleus] evidence: IC GeneID:11281 -> Cellular component: GO:0005634 [nucleus] evidence: IDA
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@meso_cacase at
DBCLS
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