2025-05-09 20:01:53, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_014468 2428 bp mRNA linear PRI 17-APR-2013 DEFINITION Homo sapiens VENT homeobox (VENTX), mRNA. ACCESSION NM_014468 VERSION NM_014468.2 GI:33356561 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 2428) AUTHORS Gao,H., Wu,X., Sun,Y., Zhou,S., Silberstein,L.E. and Zhu,Z. TITLE Suppression of homeobox transcription factor VentX promotes expansion of human hematopoietic stem/multipotent progenitor cells JOURNAL J. Biol. Chem. 287 (35), 29979-29987 (2012) PUBMED 22791709 REMARK GeneRIF: VentX regulates critical cell cycle regulators and Wnt downstream genes previously implicated in HSC/MPP proliferation and expansion. REFERENCE 2 (bases 1 to 2428) AUTHORS Wu,X., Gao,H., Ke,W., Giese,R.W. and Zhu,Z. TITLE The homeobox transcription factor VentX controls human macrophage terminal differentiation and proinflammatory activation JOURNAL J. Clin. Invest. 121 (7), 2599-2613 (2011) PUBMED 21670496 REMARK GeneRIF: Results provide mechanistic insight into the crucial roles of VentX in macrophage differentiation and proinflammatory activation and suggest that dysregulation of VentX may play a role in the pathogenesis of autoimmune diseases. REFERENCE 3 (bases 1 to 2428) AUTHORS Wu,X., Gao,H., Ke,W., Hager,M., Xiao,S., Freeman,M.R. and Zhu,Z. TITLE VentX trans-activates p53 and p16ink4a to regulate cellular senescence JOURNAL J. Biol. Chem. 286 (14), 12693-12701 (2011) PUBMED 21325273 REMARK GeneRIF: Data show that VentX is a direct transcriptional activator of p53-p21 and p16ink4a-Rb tumor suppression pathways. REFERENCE 4 (bases 1 to 2428) AUTHORS Rawat,V.P., Arseni,N., Ahmed,F., Mulaw,M.A., Thoene,S., Heilmeier,B., Sadlon,T., D'Andrea,R.J., Hiddemann,W., Bohlander,S.K., Buske,C. and Feuring-Buske,M. TITLE The vent-like homeobox gene VENTX promotes human myeloid differentiation and is highly expressed in acute myeloid leukemia JOURNAL Proc. Natl. Acad. Sci. U.S.A. 107 (39), 16946-16951 (2010) PUBMED 20833819 REMARK GeneRIF: these data extend our insights into the function of embryonic mesodermal factors in human postnatal hematopoiesis and indicate a role for VENTX in normal and malignant myelopoiesis. REFERENCE 5 (bases 1 to 2428) AUTHORS Gao,H., Le,Y., Wu,X., Silberstein,L.E., Giese,R.W. and Zhu,Z. TITLE VentX, a novel lymphoid-enhancing factor/T-cell factor-associated transcription repressor, is a putative tumor suppressor JOURNAL Cancer Res. 70 (1), 202-211 (2010) PUBMED 20028861 REMARK GeneRIF: a potential role of VentX in the clinical behavior of hematopoietic malignancies. REFERENCE 6 (bases 1 to 2428) AUTHORS Holland,P.W., Booth,H.A. and Bruford,E.A. TITLE Classification and nomenclature of all human homeobox genes JOURNAL BMC Biol. 5, 47 (2007) PUBMED 17963489 REMARK Publication Status: Online-Only REFERENCE 7 (bases 1 to 2428) AUTHORS Moretti,P.A., Davidson,A.J., Baker,E., Lilley,B., Zon,L.I. and D'Andrea,R.J. TITLE Molecular cloning of a human Vent-like homeobox gene JOURNAL Genomics 76 (1-3), 21-29 (2001) PUBMED 11549314 REFERENCE 8 (bases 1 to 2428) AUTHORS Moreau-Aubry,A., Le Guiner,S., Labarriere,N., Gesnel,M.C., Jotereau,F. and Breathnach,R. TITLE A processed pseudogene codes for a new antigen recognized by a CD8(+) T cell clone on melanoma JOURNAL J. Exp. Med. 191 (9), 1617-1624 (2000) PUBMED 10790436 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AF068006.1. On Jul 31, 2003 this sequence version replaced gi:7657179. Summary: This gene encodes a member of the Vent family of homeodomain proteins. The encoded protein may function as a transcriptional repressor and be involved in mesodermal patterning and hemopoietic stem cell maintenance. Multiple pseudogenes exist for this gene. A transcribed pseudogene located on chromosome X may lead to antigen production in certain melanomas. [provided by RefSeq, Jul 2008]. ##Evidence-Data-START## Transcript exon combination :: AF068006.1, BC108915.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025089 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. FEATURES Location/Qualifiers source 1..2428 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="10" /map="10q26.3" gene 1..2428 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /note="VENT homeobox" /db_xref="GeneID:27287" /db_xref="HGNC:13639" /db_xref="HPRD:06197" /db_xref="MIM:607158" STS 1..867 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /db_xref="UniSTS:482694" exon 1..252 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /inference="alignment:Splign:1.39.8" CDS 12..788 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /note="VENT-like homeobox 2; hemopoietic progenitor homeobox protein VENTX2; VENT-like homeobox protein 2; VENT homeobox homolog" /codon_start=1 /product="homeobox protein VENTX" /protein_id="NP_055283.1" /db_xref="GI:7657180" /db_xref="CCDS:CCDS7675.1" /db_xref="GeneID:27287" /db_xref="HGNC:13639" /db_xref="HPRD:06197" /db_xref="MIM:607158" /translation="
MRLSSSPPRGPQQLSSFGSVDWLSQSSCSGPTHTPRPADFSLGSLPGPGQTSGAREPPQAVSIKEAAGSSNLPAPERTMAGLSKEPNTLRAPRVRTAFTMEQVRTLEGVFQHHQYLSPLERKRLAREMQLSEVQIKTWFQNRRMKHKRQMQDPQLHSPFSGSLHAPPAFYSTSSGLANGLQLLCPWAPLSGPQALMLPPGSFWGLCQVAQEALASAGASCCGQPLASHPPTPGRPSLGPALSTGPRGLCAMPQTGDAF
" misc_feature 285..461 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /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(285..299,303..305,354..356,372..374,411..413, 417..422,429..434,438..446,450..455) /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /note="DNA binding site [nucleotide binding]" /db_xref="CDD:28970" misc_feature order(291..293,300..302,420..422,429..434,441..443) /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /note="specific DNA base contacts [nucleotide binding]; other site" /db_xref="CDD:28970" variation 15 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="g" /db_xref="dbSNP:199772075" variation 18 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="t" /db_xref="dbSNP:201492574" variation 20 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="g" /db_xref="dbSNP:376421544" variation 58 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:376983658" variation 116 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="t" /db_xref="dbSNP:182428049" variation 136 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:2240892" variation 155 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="t" /db_xref="dbSNP:2998143" variation 211 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="t" /db_xref="dbSNP:187903764" variation 239 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:2980723" variation 246 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="t" /db_xref="dbSNP:2240891" variation 250 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="c" /db_xref="dbSNP:11101654" exon 253..413 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /inference="alignment:Splign:1.39.8" variation 280 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:143012982" variation 295 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="g" /replace="t" /db_xref="dbSNP:199909978" variation 306 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="t" /db_xref="dbSNP:201030457" variation 312 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="t" /db_xref="dbSNP:2270192" variation 321 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="t" /db_xref="dbSNP:200741264" variation 330 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="g" /db_xref="dbSNP:202117116" variation 333 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:199908152" variation 334 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:140323759" variation 336 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:145066836" variation 343 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:200465354" variation 344 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:138892673" variation 350 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="t" /db_xref="dbSNP:140601214" variation 353 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="g" /db_xref="dbSNP:201738584" variation 364 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="t" /db_xref="dbSNP:139243086" variation 373 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:367704244" variation 376 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:375415515" variation 382 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="t" /db_xref="dbSNP:141512959" variation 389 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:201681779" exon 414..2411 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /inference="alignment:Splign:1.39.8" variation 421 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="c" /db_xref="dbSNP:376849886" variation 435 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="t" /db_xref="dbSNP:375001040" variation 436 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="g" /db_xref="dbSNP:45620332" variation 438 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="t" /db_xref="dbSNP:150884840" variation 453 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="g" /db_xref="dbSNP:45485699" variation 454 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:368423943" variation 491 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="g" /db_xref="dbSNP:139394666" variation 497 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="t" /db_xref="dbSNP:45619335" variation 505 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="t" /db_xref="dbSNP:150065198" variation 544 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:180762061" variation 552 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="t" /db_xref="dbSNP:143679708" variation 582 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:9418952" variation 614 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="c" /db_xref="dbSNP:376205046" variation 659 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:369681310" variation 660 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="g" /replace="t" /db_xref="dbSNP:56330340" variation 681 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="" /replace="g" /db_xref="dbSNP:34603733" variation 688 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="c" /db_xref="dbSNP:74164127" variation 689 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:376006983" variation 699 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="c" /db_xref="dbSNP:9419033" variation 711 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="t" /db_xref="dbSNP:373626771" variation 734 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="g" /db_xref="dbSNP:56130458" variation 751 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:9418953" variation 762 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:148086757" variation 773 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="" /replace="g" /db_xref="dbSNP:376398632" variation 793 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="g" /db_xref="dbSNP:201366555" variation 814 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:377322248" variation 837 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="c" /db_xref="dbSNP:368158537" variation 852 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="t" /db_xref="dbSNP:73390648" variation 856..858 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="" /replace="gtt" /db_xref="dbSNP:112263035" variation 958 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:9419034" variation 995..996 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="" /replace="at" /db_xref="dbSNP:201700480" variation 999..1000 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="" /replace="atgt" /db_xref="dbSNP:56081825" variation 1006..1007 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="" /replace="tgtatata" /db_xref="dbSNP:142105196" variation 1008 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:12246359" variation 1021..1022 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="" /replace="a" /replace="ata" /db_xref="dbSNP:55710246" variation 1022..1023 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="" /replace="a" /db_xref="dbSNP:56317293" variation 1022 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="t" /db_xref="dbSNP:56025417" variation 1024 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="t" /db_xref="dbSNP:55663806" variation 1026 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="t" /db_xref="dbSNP:71503788" variation 1027..1028 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="" /replace="t" /db_xref="dbSNP:71474726" variation 1028 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="t" /db_xref="dbSNP:200581875" STS 1098..1167 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /standard_name="D1S1423" /db_xref="UniSTS:149619" variation 1129 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:55853150" variation 1131 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="g" /replace="t" /db_xref="dbSNP:150261412" variation 1151 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:9419035" variation 1159 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:9419036" variation 1173 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="t" /db_xref="dbSNP:113156182" variation 1175 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:189527177" variation 1187 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:375851960" variation 1454 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:147506007" variation 1485 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:2980727" variation 1501 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:9419037" variation 1576 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="t" /db_xref="dbSNP:374718971" variation 1612 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:181401440" variation 1676 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="g" /db_xref="dbSNP:186539344" variation 1765 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="t" /db_xref="dbSNP:114178740" variation 1834 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="g" /db_xref="dbSNP:9418954" variation 1882 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="t" /db_xref="dbSNP:2980729" variation 1888 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="t" /db_xref="dbSNP:115812110" variation 1931 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="g" /db_xref="dbSNP:75906645" variation 1946 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:190318869" variation 1996 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:181809403" variation 2036 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:2980730" variation 2039 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:2980731" variation 2051 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:149482998" variation 2061 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:2980732" variation 2067 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="t" /db_xref="dbSNP:143874903" variation 2079 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:41313485" variation 2125 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="g" /db_xref="dbSNP:148601212" variation 2159 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="t" /db_xref="dbSNP:142229661" variation 2229 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="t" /db_xref="dbSNP:3750849" variation 2238 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:370842374" variation 2269 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:146747596" variation 2272 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="t" /db_xref="dbSNP:74164129" variation 2290 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="c" /replace="g" /db_xref="dbSNP:2998120" variation 2327 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" /replace="a" /replace="g" /db_xref="dbSNP:1054776" polyA_site 2411 /gene="VENTX" /gene_synonym="HPX42B; NA88A; VENTX2" ORIGIN
acctggccgccatgcgcctctcctcctccccacctcgtggcccgcagcagctctccagctttggctccgtggactggctctcccagagcagctgctcagggccgacccacacccccaggcctgccgacttctccctggggagcctccctggcccaggccagacatccggcgcccgggagccccctcaggccgtcagcatcaaggaggccgccgggtcctcaaatctgcctgcgccggagaggaccatggccgggttgagtaaggagccaaataccttgcgggccccccgtgtccgcacagccttcaccatggagcaggtccgcaccttggagggcgtcttccagcaccaccagtacctgagccctctggagcggaagaggctggccagggagatgcagctctcagaggtccagataaaaacctggtttcagaatcgccgcatgaaacacaaacggcaaatgcaggacccccagctgcacagccccttctcggggtctctccatgcgcccccagctttctactcaacgtcttctggccttgccaatggcctgcagctgctgtgcccttgggcacccctgtccgggccccaggctctgatgctgccccctggctccttctggggtctctgccaagtggcacaagaggccctggcatctgcgggagcttcctgctgcgggcagcctctggcgtcccacccccctaccccaggccggccttcgctgggaccagccctgtccacggggccccggggcctgtgtgctatgccacagacgggggatgcattttgaggaggcacctctgactcccacactcgcggtcttgctgatcgcacctggctcctacctggaggactcagttgttctgtttacatcctggtggcacctctcaccctgacccacacaaaggttctggagattactggagaatatatataaatatatatatgtacgtatatatgtaaatacacatatacgtatatataaatatatatatacatatgtgtgtgtatatatatatatatttttttttttttttttttttttgagacggagtgttgctctgtcacccaggctggagtgcaatgacgcaatctcggctcactgcaacctccgcctcctgggttcaagcgattctccagcctcagcctcccgagtagctgggattacagacacccgccaccacgcccggctaattttttctatttttagtagaaatggggtttcaccatgttagccaggctggtctcaaactcctgaccctgtgatccgcccgcctcggcctcccaaagtgctgggattacaggcatgagccactgcacccggccctgagaatatatttattaaagccacctcttcactgaaagttaccgaaagagtcggtttaggaaggaaacgaagggtcagtgaacagagtcaaatgcagaagtgggcttgtcatgggtagggctttcggcgtacgataaaaggatcatttgttttttaaaaggggttggaaaaactggttttccagttggaaacagtaaaggttgtaagctttgtgtgtacaaaagaaaacagggaatgcaggtgtgtttatagcgttgtggttcaagtccctcttaacaagaactccaaagctggaaagcaggagggaacaaaggtgaacatgaaggcgaggatgctggggccctgcagtgcgctctaggctgtgcgtgagccgggactgtacccacagcttgctgagggctgctcttcttgggccagggaaagcagggcagccgggacctgcggctgtgcctggactgaagctgtcccgcaggtccccaccctccaacacgtgctcacctgtccccctcctcgcagcagcctcgggacaaaacaatgactcaaggacagcacttctcgcagaaggtctggaagtgcccagaatgggaggcacggaagcccctcccggggaggactcccgcgttgatggaccgttcttggtgcagactcctgactgcgtgcatgaaacctgagacaagtgcaattccttccatgtcgccccagagtgcccaggaggcaggcagtgcggggtgcccaggcagacgggttcagcctgcagaactggaggcgacctgtgaaacccacccgggcaccccaacaggaacagaagcgtggtcctgcggctgcgtccccagcgagtttcactttccccttgctcgtttctcccttgttgtaagtgtttacaactggcatgtgcttttaaacgtcaggtaagaggggaacagctgctgtacatcgtcctggcgagtgacaatgtgacagaagcctgggcgaggccctcggagggcagcagctggacaggggctactgggtttggcctggacagcactgatttgtggatgtggatgggggcacgttgtccgtgataaaagtacaagtgcccctcacaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:27287 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: IEA GeneID:27287 -> Molecular function: GO:0043565 [sequence-specific DNA binding] evidence: IEA GeneID:27287 -> Biological process: GO:0007275 [multicellular organismal development] evidence: IEA GeneID:27287 -> Cellular component: GO:0005634 [nucleus] evidence: IEA
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