2025-05-09 19:15:45, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_004575 3141 bp mRNA linear PRI 16-JUN-2013 DEFINITION Homo sapiens POU class 4 homeobox 2 (POU4F2), mRNA. ACCESSION NM_004575 VERSION NM_004575.2 GI:110347454 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 3141) AUTHORS Reinert,T., Borre,M., Christiansen,A., Hermann,G.G., Orntoft,T.F. and Dyrskjot,L. TITLE Diagnosis of bladder cancer recurrence based on urinary levels of EOMES, HOXA9, POU4F2, TWIST1, VIM, and ZNF154 hypermethylation JOURNAL PLoS ONE 7 (10), E46297 (2012) PUBMED 23056278 REMARK GeneRIF: Methylation levels of EOMES, HOXA9, POU4F2, TWIST1, VIM, and ZNF154 in urine specimens are promising diagnostic biomarkers for bladder cancer recurrence surveillance REFERENCE 2 (bases 1 to 3141) AUTHORS Fujita,R., Ounzain,S., Wang,A.C., Heads,R.J. and Budhram-Mahadeo,V.S. TITLE Hsp-27 induction requires POU4F2/Brn-3b TF in doxorubicin-treated breast cancer cells, whereas phosphorylation alters its cellular localisation following drug treatment JOURNAL Cell Stress Chaperones 16 (4), 427-439 (2011) PUBMED 21279488 REFERENCE 3 (bases 1 to 3141) AUTHORS Qiu,F., Jiang,H. and Xiang,M. TITLE A comprehensive negative regulatory program controlled by Brn3b to ensure ganglion cell specification from multipotential retinal precursors JOURNAL J. Neurosci. 28 (13), 3392-3403 (2008) PUBMED 18367606 REMARK GeneRIF: Brn3b specifies the RGC fate from multipotential precursors not only by promoting RGC differentiation but also by suppressing non-RGC differentiation programs as a safeguard mechanism. REFERENCE 4 (bases 1 to 3141) AUTHORS Budhram-Mahadeo,V.S., Irshad,S., Bowen,S., Lee,S.A., Samady,L., Tonini,G.P. and Latchman,D.S. TITLE Proliferation-associated Brn-3b transcription factor can activate cyclin D1 expression in neuroblastoma and breast cancer cells JOURNAL Oncogene 27 (1), 145-154 (2008) PUBMED 17637757 REMARK GeneRIF: May act to alter growth properties of breast cancer and neuroblastoma cells by enhancing cyclin D1 expression in these tumor cells. REFERENCE 5 (bases 1 to 3141) AUTHORS Calissano,M., Diss,J.K. and Latchman,D.S. TITLE Post-transcriptional regulation of the Brn-3b transcription factor in differentiating neuroblastoma cells JOURNAL FEBS Lett. 581 (13), 2490-2496 (2007) PUBMED 17490655 REMARK GeneRIF: Two different microRNAs that potentially regulate the stability of Brn-3b have been identified in neuroblastoma cells. REFERENCE 6 (bases 1 to 3141) AUTHORS Smith,M.D., Dawson,S.J. and Latchman,D.S. TITLE Inhibition of neuronal process outgrowth and neuronal specific gene activation by the Brn-3b transcription factor JOURNAL J. Biol. Chem. 272 (2), 1382-1388 (1997) PUBMED 8995448 REFERENCE 7 (bases 1 to 3141) AUTHORS Xiang,M., Zhou,L., Macke,J.P., Yoshioka,T., Hendry,S.H., Eddy,R.L., Shows,T.B. and Nathans,J. TITLE The Brn-3 family of POU-domain factors: primary structure, binding specificity, and expression in subsets of retinal ganglion cells and somatosensory neurons JOURNAL J. Neurosci. 15 (7 PT 1), 4762-4785 (1995) PUBMED 7623109 REFERENCE 8 (bases 1 to 3141) AUTHORS Bhargava,A.K., Li,Z. and Weissman,S.M. TITLE Differential expression of four members of the POU family of proteins in activated and phorbol 12-myristate 13-acetate-treated Jurkat T cells JOURNAL Proc. Natl. Acad. Sci. U.S.A. 90 (21), 10260-10264 (1993) PUBMED 8234287 REFERENCE 9 (bases 1 to 3141) AUTHORS Xiang,M., Zhou,L., Peng,Y.W., Eddy,R.L., Shows,T.B. and Nathans,J. TITLE Brn-3b: a POU domain gene expressed in a subset of retinal ganglion cells JOURNAL Neuron 11 (4), 689-701 (1993) PUBMED 7691107 REFERENCE 10 (bases 1 to 3141) AUTHORS Ring,C.J. and Latchman,D.S. TITLE The human Brn-3b POU transcription factor shows only limited homology to the Brn-3a/RDC-1 factor outside the conserved POU domain JOURNAL Nucleic Acids Res. 21 (12), 2946 (1993) PUBMED 8332509 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from DB082745.1, BY796838.2, U06233.1 and X71488.1. On Jul 14, 2006 this sequence version replaced gi:4758947. Summary: The protein encoded by this gene is a member of the POU-domain transcription factor family and may be involved in maintaining visual system neurons in the retina. The level of the encoded protein is also elevated in a majority of breast cancers, resulting in accelerated tumor growth. [provided by RefSeq, Sep 2011]. 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 :: U06233.1, EU439706.1 [ECO:0000332] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-448 DB082745.1 1-448 449-638 BY796838.2 438-627 639-741 U06233.1 606-708 742-793 X71488.1 62-113 794-2552 U06233.1 761-2519 2553-3141 U06233.1 2522-3110 FEATURES Location/Qualifiers source 1..3141 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="4" /map="4q31.2" gene 1..3141 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /note="POU class 4 homeobox 2" /db_xref="GeneID:5458" /db_xref="HGNC:9219" /db_xref="MIM:113725" exon 1..536 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /inference="alignment:Splign:1.39.8" variation 21 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="g" /replace="t" /db_xref="dbSNP:143373833" variation 97 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:370191425" variation 112 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="g" /replace="t" /db_xref="dbSNP:372544942" variation 155 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:35733768" variation 194 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:369199465" variation 200 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:369625548" STS 202..1531 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /db_xref="UniSTS:482508" variation 209 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="g" /db_xref="dbSNP:373501732" misc_feature 210..212 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /note="upstream in-frame stop codon" variation 217 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:376572394" variation 243 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:202046663" CDS 249..1478 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /note="Brn3b POU domain transcription factor; POU domain protein; POU domain class 4 transcription factor 2; brain-3B; brain-specific homeobox/POU domain protein 3B" /codon_start=1 /product="POU domain, class 4, transcription factor 2" /protein_id="NP_004566.2" /db_xref="GI:110347455" /db_xref="CCDS:CCDS34074.1" /db_xref="GeneID:5458" /db_xref="HGNC:9219" /db_xref="MIM:113725" /translation="
MMMMSLNSKQAFSMPHGGSLHVEPKYSALHSTSPGSSAPIAPSASSPSSSSNAGGGGGGGGGGGGGGGRSSSSSSSGSSGGGGSEAMRRACLPTPPSNIFGGLDESLLARAEALAAVDIVSQSKSHHHHPPHHSPFKPDATYHTMNTIPCTSAASSSSVPISHPSALAGTHHHHHHHHHHHHQPHQALEGELLEHLSPGLALGAMAGPDGAVVSTPAHAPHMATMNPMHQAALSMAHAHGLPSHMGCMSDVDADPRDLEAFAERFKQRRIKLGVTQADVGSALANLKIPGVGSLSQSTICRFESLTLSHNNMIALKPILQAWLEEAEKSHREKLTKPELFNGAEKKRKRTSIAAPEKRSLEAYFAIQPRPSSEKIAAIAEKLDLKKNVVRVWFCNQRQKQKRMKYSAGI
" misc_feature 576..605 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (Q12837.2); Region: POU-IV box" misc_feature 996..1229 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /note="Found in Pit-Oct-Unc transcription factors; Region: POU; smart00352" /db_xref="CDD:197673" misc_feature 1284..1460 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /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(1284..1298,1302..1304,1353..1355,1371..1373, 1410..1412,1416..1421,1428..1433,1437..1445,1449..1454) /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /note="DNA binding site [nucleotide binding]" /db_xref="CDD:28970" misc_feature order(1290..1292,1299..1301,1419..1421,1428..1433, 1440..1442) /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /note="specific DNA base contacts [nucleotide binding]; other site" /db_xref="CDD:28970" variation 275 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:200843721" variation 293 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="g" /replace="t" /db_xref="dbSNP:146671454" variation 294 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="c" /db_xref="dbSNP:62327967" variation 296 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="c" /db_xref="dbSNP:369358968" variation 319 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:199899657" variation 338 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:373682041" variation 344 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:140261687" variation 367 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:13152799" variation 372 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:184591480" variation 414..422 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="" /replace="ggcggcggc" /replace="ggcggcggcggc" /db_xref="dbSNP:67907220" variation 414..415 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="" /replace="ggc" /db_xref="dbSNP:72269802" variation 416 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:189899086" variation 438..446 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="" /replace="ggcggcggc" /db_xref="dbSNP:67194443" variation 438..439 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="" /replace="ggc" /replace="ggcggcggcggcggc" /db_xref="dbSNP:34359247" variation 449..450 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="" /replace="cgg" /db_xref="dbSNP:33986795" variation 482 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="g" /db_xref="dbSNP:199600550" variation 508 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:145352817" variation 513 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="c" /db_xref="dbSNP:148020860" variation 532 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:141725106" exon 537..3141 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /inference="alignment:Splign:1.39.8" variation 544 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:201496393" variation 625 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:372609971" variation 640 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:150150229" variation 665 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="c" /db_xref="dbSNP:147517729" variation 666 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:74417037" variation 695 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:143938073" variation 707 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:139883264" variation 752 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:143876216" variation 764 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:369535679" variation 768 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="c" /db_xref="dbSNP:376900695" variation 798 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:144284868" variation 809 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:376581460" variation 828 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:371559221" variation 851 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:200464919" variation 862 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:373979098" variation 866 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:202030431" variation 878 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:376822201" variation 893 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:200695260" variation 899 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="g" /replace="t" /db_xref="dbSNP:373088055" variation 915 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:377219455" variation 943 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:376992021" variation 962 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:148751103" variation 965 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="c" /db_xref="dbSNP:373594627" variation 991 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="g" /replace="t" /db_xref="dbSNP:373360428" variation 1005 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:3827593" variation 1059 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="c" /db_xref="dbSNP:200579530" variation 1065 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="g" /db_xref="dbSNP:142395313" variation 1073 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="c" /db_xref="dbSNP:151303999" variation 1095 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:76129457" variation 1105 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="t" /db_xref="dbSNP:373485818" variation 1107 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="c" /db_xref="dbSNP:376482978" variation 1114 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="g" /db_xref="dbSNP:144507526" variation 1119 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:369337694" variation 1122 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:372535541" variation 1123 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="g" /replace="t" /db_xref="dbSNP:200312228" variation 1126 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:371120198" variation 1172 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="g" /db_xref="dbSNP:3827594" variation 1190 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="g" /replace="t" /db_xref="dbSNP:61733420" variation 1209 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:145278389" variation 1238 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:144940288" variation 1246 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="c" /db_xref="dbSNP:199979947" variation 1275 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:377411656" variation 1277 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="g" /replace="t" /db_xref="dbSNP:370767940" variation 1278 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:375025437" variation 1298 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="g" /replace="t" /db_xref="dbSNP:371952832" variation 1306 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="g" /db_xref="dbSNP:200705430" variation 1308 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:374901217" variation 1310 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:367653245" variation 1313 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:61733419" variation 1328 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="g" /db_xref="dbSNP:143117935" variation 1334 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:148247830" variation 1341 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="g" /replace="t" /db_xref="dbSNP:180935169" variation 1344 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:142851123" variation 1349 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="g" /db_xref="dbSNP:372860552" variation 1358 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:199813288" variation 1374 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:147007829" variation 1376 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:200415873" variation 1385 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:369917575" variation 1409 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="c" /db_xref="dbSNP:138240408" variation 1432 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:113095745" variation 1453 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="g" /replace="t" /db_xref="dbSNP:201841354" variation 1466 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:370757448" variation 1469 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:143812023" STS 1486..1618 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /standard_name="G34464" /db_xref="UniSTS:80252" variation 1489 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="g" /replace="t" /db_xref="dbSNP:3810843" variation 1503 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:376016201" variation 1508 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="g" /replace="t" /db_xref="dbSNP:370553185" variation 1613 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:368127169" variation 1663 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:372340520" variation 1690 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="t" /db_xref="dbSNP:369146164" STS 1765..1859 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /standard_name="D4S3267" /db_xref="UniSTS:76043" variation 1840 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:376565147" variation 1850 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="" /replace="c" /db_xref="dbSNP:201294453" variation 1989 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="g" /replace="t" /db_xref="dbSNP:72956271" variation 2013 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:76180708" variation 2091 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:186245328" variation 2216 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:139670347" variation 2280 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:114364181" variation 2423 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:7669891" variation 2494 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:372851210" STS 2502..2699 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /standard_name="D4S3346" /db_xref="UniSTS:24323" variation 2526..2527 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="" /replace="ac" /replace="acacac" /db_xref="dbSNP:71592457" variation 2526 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:200297474" variation 2527..2528 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="" /replace="ac" /db_xref="dbSNP:375277243" variation 2528..2529 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="" /replace="ca" /replace="cacacaca" /db_xref="dbSNP:72274820" variation 2541..2542 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="" /replace="ca" /db_xref="dbSNP:10682779" variation 2542..2543 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="" /replace="ca" /replace="cacacaca" /db_xref="dbSNP:35584951" variation 2543..2544 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="" /replace="ac" /replace="acac" /replace="acacacac" /db_xref="dbSNP:34459995" variation 2590 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:6825713" variation 2595 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:111877076" variation 2665 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:191340422" variation 2777 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:183140735" variation 2841 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="g" /replace="t" /db_xref="dbSNP:369169254" variation 2846 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="c" /db_xref="dbSNP:186059151" variation 2919 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:144585453" variation 2978 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="a" /replace="g" /db_xref="dbSNP:74571172" variation 3092 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /replace="c" /replace="t" /db_xref="dbSNP:190835038" polyA_site 3141 /gene="POU4F2" /gene_synonym="Brn-3b; BRN3.2; BRN3B" /note="19 A residues" ORIGIN
agtttcgggtgccgaggtctgcagctagcggcaagcggagtcaggcatccgttcagactgacagcagaggcggcgaaggagcgcgtagccgagatcaggcgtacagagtccggaggcggcggcgggtgagctcaacttcgcacagcccttcccagctccagccccggctggcccggcacttctcggagggtcccggcagccgggaccagtgagtgcctctacggaccagcgccccggcgggcgggaagatgatgatgatgtccctgaacagcaagcaggcgtttagcatgccgcacggcggcagcctgcacgtggagcccaagtactcggcactgcacagcacctcgccgggctcctcggctcccatcgcgccctcggccagctcccccagcagctcgagcaacgctggtggtggcggcggcggcggcggcggcggcggcggcggcggaggccgaagcagcagctccagcagcagtggcagcagcggcggcgggggctcggaggctatgcggagagcctgtcttccaaccccaccgagcaatatattcggcgggctggatgagagtctgctggcccgcgccgaggctctggcagccgtggacatcgtctcccagagcaagagccaccaccaccatccaccccaccacagccccttcaaaccggacgccacctaccacactatgaataccatcccgtgcacgtcggccgcctcttcttcatcggtgcccatctcgcacccttccgcgttggcgggcacgcaccaccaccaccaccatcaccaccaccaccaccaccaaccgcaccaggcgctggagggcgagctgctggagcacctgagtcccgggctggccctgggcgctatggcgggccccgacggcgctgtggtgtccacgccggctcacgcgccgcacatggccaccatgaaccccatgcaccaagcagcgctcagcatggcccacgcgcacgggctgccgtcgcacatgggctgcatgagcgacgtggacgccgacccgcgggacctggaggcattcgccgagcgcttcaagcagcgacgcatcaagctgggggtgacccaggcagatgtgggctccgcgctggccaacctcaagatccccggcgtgggctcgcttagccagagcaccatctgcaggttcgagtccctcacactgtcccacaataatatgatcgcgctcaaacccatcctgcaggcatggctcgaggaggccgagaagtcccaccgcgagaagctcaccaagcctgaactcttcaatggcgcggagaagaagcgcaagcgcacgtccatcgctgcgccagagaagcgctcgctcgaagcctactttgccattcagcctcggccctcctctgaaaagatcgccgccatcgcggagaagctggacctgaagaaaaacgtggtgcgcgtctggttctgcaaccagaggcagaaacagaaaagaatgaaatattccgccggcatttagaagactcttggcctctccagagacgcccctttcctcgtccgctcttttctctcctctcttctgcctcttttcacttttggcgactagaaacaattccagtaaatgtgaatctcgacaaatcgaggactgaagagggagcgaacgagcgaacaactgagcccaagccggtgagaatgtgaaacagtttctcaaaggaaagaataacaaaagatggtatttgtctgttgtagcaaagttgtccctttgaaccccacctcggcttcttcagaggaagtgtggagatggctgtttgcaggaaggcagacgagacagtgtttaaaaagtccacaagaatgatcaagtaagatttgtttttattcttacagacatcacccgtgttcaagtttaaaagtacactttgcaactatttttcagaaatagaaattgattcaggactaaaactttaaactagagttgatgcttaatgtgatagagacatctctaaagtattttgaattttaaaaaaagatggcagattttctgcatttacactgtatattatatatatatttttattgtggttcttacccccttttccttctctgaagtgttaatgcttaagaaaagagttgcgcctgctgtgttcactgatcttgaaagctattattagattattgcagaacaaccctctgtaaattattaatttatctctctagcaacttaattttgtgcacattctaattaattaaacttcttccgtctaaaaaaagtgggggaaatgtatagctagtaacgttcaaaaaattttgtttgatgagtttaccgaatttttacagctttcctcctatactgtgttccttttgacccatttgtatattctcacttgaatgaagattgtttttttctttgtttttactggtagtgttctgatttgtgagtcgacactcagtaatggatgtcttaatcgtgtagacctgattcactgtctgaagtattgtttacttcgttacatatttaatggggattcccacattgtccccatgacacatgagcgctctcacttacccttacacacacacacacacacacacacacctctaacagaagggaagaagcagttggaagcatgaccgatgcaccattttctagttttaggtgcatttgccacttggtgtttgcccttcagattttagatttcaccaaggtatttcagtcttccagttttcaattgctttgttggctacatgttaatatttataggaatacttcagtttttccttttggaggtttgtttgtagaaaaactaatttgaactataagaaagacagtgcactgcttgtaaattcacattgtttggaaaaattcttttggaacaaaaaattaggtacatgataactggtaccttatctactgtaaatatttcattaaaaatgatgcacacatagatatattcttacaaattttgctgtattgctgttctctttgaggctctccaaagtcttgagttctgtatatggcctggtttcttgtttttattaatagatggtttatttactatggtaatgtattaatttatttttggtgttgttcgattgtctttcattgaagagataattttaatgttttattggcaacgtatgctgctttttcattaaaatatgctattaaaattaaatggctttta
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:5458 -> Molecular function: GO:0000978 [RNA polymerase II core promoter proximal region sequence-specific DNA binding] evidence: IDA GeneID:5458 -> Molecular function: GO:0001077 [RNA polymerase II core promoter proximal region sequence-specific DNA binding transcription factor activity involved in positive regulation of transcription] evidence: IDA GeneID:5458 -> Molecular function: GO:0001078 [RNA polymerase II core promoter proximal region sequence-specific DNA binding transcription factor activity involved in negative regulation of transcription] evidence: ISS GeneID:5458 -> Molecular function: GO:0003682 [chromatin binding] evidence: IEA GeneID:5458 -> Biological process: GO:0000122 [negative regulation of transcription from RNA polymerase II promoter] evidence: ISS GeneID:5458 -> Biological process: GO:0000165 [MAPK cascade] evidence: IDA GeneID:5458 -> Biological process: GO:0007411 [axon guidance] evidence: ISS GeneID:5458 -> Biological process: GO:0007605 [sensory perception of sound] evidence: IEA GeneID:5458 -> Biological process: GO:0030182 [neuron differentiation] evidence: ISS GeneID:5458 -> Biological process: GO:0030520 [intracellular estrogen receptor signaling pathway] evidence: IDA GeneID:5458 -> Biological process: GO:0031290 [retinal ganglion cell axon guidance] evidence: IEA GeneID:5458 -> Biological process: GO:0045597 [positive regulation of cell differentiation] evidence: ISS GeneID:5458 -> Biological process: GO:0045944 [positive regulation of transcription from RNA polymerase II promoter] evidence: IDA GeneID:5458 -> Biological process: GO:0048675 [axon extension] evidence: IEA GeneID:5458 -> Biological process: GO:0050885 [neuromuscular process controlling balance] evidence: IEA GeneID:5458 -> Biological process: GO:0060041 [retina development in camera-type eye] evidence: ISS GeneID:5458 -> Cellular component: GO:0005634 [nucleus] evidence: IC GeneID:5458 -> Cellular component: GO:0005634 [nucleus] evidence: ISS GeneID:5458 -> Cellular component: GO:0016607 [nuclear speck] evidence: IEA
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