2025-05-09 19:34:18, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_006898 2319 bp mRNA linear PRI 17-APR-2013 DEFINITION Homo sapiens homeobox D3 (HOXD3), mRNA. ACCESSION NM_006898 VERSION NM_006898.4 GI:23510372 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 2319) AUTHORS Shaoqiang,C., Yue,Z., Yang,L., Hong,Z., Lina,Z., Da,P. and Qingyuan,Z. TITLE Expression of HOXD3 correlates with shorter survival in patients with invasive breast cancer JOURNAL Clin. Exp. Metastasis 30 (2), 155-163 (2013) PUBMED 22935821 REMARK GeneRIF: High expression of HOXD3 correlates with invasive breast cancer. REFERENCE 2 (bases 1 to 2319) AUTHORS Liu,L., Kron,K.J., Pethe,V.V., Demetrashvili,N., Nesbitt,M.E., Trachtenberg,J., Ozcelik,H., Fleshner,N.E., Briollais,L., van der Kwast,T.H. and Bapat,B. TITLE Association of tissue promoter methylation levels of APC, TGFbeta2, HOXD3 and RASSF1A with prostate cancer progression JOURNAL Int. J. Cancer 129 (10), 2454-2462 (2011) PUBMED 21207416 REMARK GeneRIF: quantitative increase in promoter methylation levels of HOXD3 is associated with prostate cancer progression REFERENCE 3 (bases 1 to 2319) AUTHORS Goode,E.L., Chenevix-Trench,G., Song,H., Ramus,S.J., Notaridou,M., Lawrenson,K., Widschwendter,M., Vierkant,R.A., Larson,M.C., Kjaer,S.K., Birrer,M.J., Berchuck,A., Schildkraut,J., Tomlinson,I., Kiemeney,L.A., Cook,L.S., Gronwald,J., Garcia-Closas,M., Gore,M.E., Campbell,I., Whittemore,A.S., Sutphen,R., Phelan,C., Anton-Culver,H., Pearce,C.L., Lambrechts,D., Rossing,M.A., Chang-Claude,J., Moysich,K.B., Goodman,M.T., Dork,T., Nevanlinna,H., Ness,R.B., Rafnar,T., Hogdall,C., Hogdall,E., Fridley,B.L., Cunningham,J.M., Sieh,W., McGuire,V., Godwin,A.K., Cramer,D.W., Hernandez,D., Levine,D., Lu,K., Iversen,E.S., Palmieri,R.T., Houlston,R., van Altena,A.M., Aben,K.K., Massuger,L.F., Brooks-Wilson,A., Kelemen,L.E., Le,N.D., Jakubowska,A., Lubinski,J., Medrek,K., Stafford,A., Easton,D.F., Tyrer,J., Bolton,K.L., Harrington,P., Eccles,D., Chen,A., Molina,A.N., Davila,B.N., Arango,H., Tsai,Y.Y., Chen,Z., Risch,H.A., McLaughlin,J., Narod,S.A., Ziogas,A., Brewster,W., Gentry-Maharaj,A., Menon,U., Wu,A.H., Stram,D.O., Pike,M.C., Beesley,J., Webb,P.M., Chen,X., Ekici,A.B., Thiel,F.C., Beckmann,M.W., Yang,H., Wentzensen,N., Lissowska,J., Fasching,P.A., Despierre,E., Amant,F., Vergote,I., Doherty,J., Hein,R., Wang-Gohrke,S., Lurie,G., Carney,M.E., Thompson,P.J., Runnebaum,I., Hillemanns,P., Durst,M., Antonenkova,N., Bogdanova,N., Leminen,A., Butzow,R., Heikkinen,T., Stefansson,K., Sulem,P., Besenbacher,S., Sellers,T.A., Gayther,S.A. and Pharoah,P.D. CONSRTM Wellcome Trust Case-Control Consortium; Australian Cancer Study (Ovarian Cancer); Australian Ovarian Cancer Study Group; Ovarian Cancer Association Consortium (OCAC); Ovarian Cancer Association Consortium (OCAC) TITLE A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24 JOURNAL Nat. Genet. 42 (10), 874-879 (2010) PUBMED 20852632 REFERENCE 4 (bases 1 to 2319) AUTHORS Kron,K.J., Liu,L., Pethe,V.V., Demetrashvili,N., Nesbitt,M.E., Trachtenberg,J., Ozcelik,H., Fleshner,N.E., Briollais,L., van der Kwast,T.H. and Bapat,B. TITLE DNA methylation of HOXD3 as a marker of prostate cancer progression JOURNAL Lab. Invest. 90 (7), 1060-1067 (2010) PUBMED 20212450 REMARK GeneRIF: HOXD3 methylation distinguishes low-grade prostate cancers from intermediate and high-grade ones. REFERENCE 5 (bases 1 to 2319) AUTHORS Ester,A.R., Weymouth,K.S., Burt,A., Wise,C.A., Scott,A., Gurnett,C.A., Dobbs,M.B., Blanton,S.H. and Hecht,J.T. TITLE Altered transmission of HOX and apoptotic SNPs identify a potential common pathway for clubfoot JOURNAL Am. J. Med. Genet. A 149A (12), 2745-2752 (2009) PUBMED 19938081 REMARK GeneRIF: Observational study of gene-disease association and gene-gene interaction. (HuGE Navigator) REFERENCE 6 (bases 1 to 2319) AUTHORS Scott,M.P. TITLE Vertebrate homeobox gene nomenclature JOURNAL Cell 71 (4), 551-553 (1992) PUBMED 1358459 REFERENCE 7 (bases 1 to 2319) AUTHORS Taniguchi,Y., Fujii,A. and Moriuchi,T. TITLE Cloning and sequencing of the human homeobox gene HOX4A JOURNAL Biochim. Biophys. Acta 1132 (3), 332-334 (1992) PUBMED 1358204 REFERENCE 8 (bases 1 to 2319) AUTHORS McAlpine,P.J. and Shows,T.B. TITLE Nomenclature for human homeobox genes JOURNAL Genomics 7 (3), 460 (1990) PUBMED 1973146 REFERENCE 9 (bases 1 to 2319) AUTHORS Acampora,D., D'Esposito,M., Faiella,A., Pannese,M., Migliaccio,E., Morelli,F., Stornaiuolo,A., Nigro,V., Simeone,A. and Boncinelli,E. TITLE The human HOX gene family JOURNAL Nucleic Acids Res. 17 (24), 10385-10402 (1989) PUBMED 2574852 REFERENCE 10 (bases 1 to 2319) AUTHORS Boncinelli,E., Acampora,D., Pannese,M., D'Esposito,M., Somma,R., Gaudino,G., Stornaiuolo,A., Cafiero,M., Faiella,A. and Simeone,A. TITLE Organization of human class I homeobox genes JOURNAL Genome 31 (2), 745-756 (1989) PUBMED 2576652 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from BC005124.2. On Oct 7, 2002 this sequence version replaced gi:19923390. Summary: This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXD genes located at 2q31-2q37 chromosome regions. Deletions that removed the entire HOXD gene cluster or 5' end of this cluster have been associated with severe limb and genital abnormalities. The protein encoded by this gene may play a role in the regulation of cell adhesion processes. [provided by RefSeq, Jul 2008]. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: BC005124.2 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025084, ERS025085 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. FEATURES Location/Qualifiers source 1..2319 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="2" /map="2q31.1" gene 1..2319 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /note="homeobox D3" /db_xref="GeneID:3232" /db_xref="HGNC:5137" /db_xref="HPRD:00863" /db_xref="MIM:142980" exon 1..92 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /inference="alignment:Splign:1.39.8" variation 25 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="g" /db_xref="dbSNP:2113562" variation 37..38 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="" /replace="a" /db_xref="dbSNP:142263809" variation 37 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="c" /db_xref="dbSNP:201023251" exon 93..717 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /inference="alignment:Splign:1.39.8" variation 113 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="t" /db_xref="dbSNP:72927183" variation 130 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="g" /replace="t" /db_xref="dbSNP:370796757" misc_feature 171..173 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /note="upstream in-frame stop codon" CDS 177..1475 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /note="homeo box D3; Hox-4.1, mouse, homolog of; homeobox protein Hox-4A" /codon_start=1 /product="homeobox protein Hox-D3" /protein_id="NP_008829.3" /db_xref="GI:19923391" /db_xref="CCDS:CCDS2270.1" /db_xref="GeneID:3232" /db_xref="HGNC:5137" /db_xref="HPRD:00863" /db_xref="MIM:142980" /translation="
MLFEQGQQALELPECTMQKAAYYENPGLFGGYGYSKTTDTYGYSTPHQPYPPPAAASSLDTDYPGSACSIQSSAPLRAPAHKGAELNGSCMRPGTGNSQGGGGGSQPPGLNSEQQPPQPPPPPPTLPPSSPTNPGGGVPAKKPKGGPNASSSSATISKQIFPWMKESRQNSKQKNSCATAGESCEDKSPPGPASKRVRTAYTSAQLVELEKEFHFNRYLCRPRRVEMANLLNLTERQIKIWFQNRRMKYKKDQKAKGILHSPASQSPERSPPLGGAAGHVAYSGQLPPVPGLAYDAPSPPAFAKSQPNMYGLAAYTAPLSSCLPQQKRYAAPEFEPHPMASNGGGFASANLQGSPVYVGGNFVESMAPASGPVFNLGHLSHPSSASVDYSCAAQIPGNHHHGPCDPHPTYTDLSAHHSSQGRLPEAPKLTHL
" misc_feature 624..986 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /note="Homeodomain-containing transcription factor [Transcription]; Region: COG5576" /db_xref="CDD:35135" misc_feature 654..671 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (P31249.3); Region: Antp-type hexapeptide" misc_feature 759..935 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /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(759..773,777..779,828..830,846..848,885..887, 891..896,903..908,912..920,924..929) /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /note="DNA binding site [nucleotide binding]" /db_xref="CDD:28970" misc_feature order(765..767,774..776,894..896,903..908,915..917) /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /note="specific DNA base contacts [nucleotide binding]; other site" /db_xref="CDD:28970" misc_feature 1278..1466 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /note="Domain of unknown function (DUF4074); Region: DUF4074; pfam13293" /db_xref="CDD:205473" variation 184 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="t" /db_xref="dbSNP:200641637" variation 186 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="g" /replace="t" /db_xref="dbSNP:201061047" variation 190 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="t" /db_xref="dbSNP:200129595" variation 260 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="g" /db_xref="dbSNP:140952976" variation 274 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="g" /db_xref="dbSNP:373609882" variation 281 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="t" /db_xref="dbSNP:199964353" variation 289 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="t" /db_xref="dbSNP:75250034" variation 290 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="g" /db_xref="dbSNP:373537603" variation 299 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="t" /db_xref="dbSNP:201012462" variation 300 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="g" /db_xref="dbSNP:138422926" variation 327 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="c" /db_xref="dbSNP:143404265" variation 329 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="c" /db_xref="dbSNP:141168805" variation 350 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="t" /db_xref="dbSNP:143525922" variation 397 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="t" /db_xref="dbSNP:372175551" variation 448 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="g" /replace="t" /db_xref="dbSNP:147184232" variation 449 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="g" /db_xref="dbSNP:145664108" variation 455 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="c" /db_xref="dbSNP:34729309" variation 464 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="g" /db_xref="dbSNP:77818566" variation 533 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="t" /db_xref="dbSNP:375537887" variation 535 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="t" /db_xref="dbSNP:190587708" variation 541 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="t" /db_xref="dbSNP:368322060" variation 547 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="t" /db_xref="dbSNP:140883088" variation 550 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="c" /db_xref="dbSNP:74698314" variation 562 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="g" /db_xref="dbSNP:1051932" variation 598 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="g" /db_xref="dbSNP:199953096" variation 650 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="g" /db_xref="dbSNP:371779084" STS 683..1035 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /standard_name="Hoxd3" /db_xref="UniSTS:158733" variation 698 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="g" /db_xref="dbSNP:376541904" exon 718..2299 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /inference="alignment:Splign:1.39.8" variation 739 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="g" /db_xref="dbSNP:137915443" variation 757 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="g" /db_xref="dbSNP:369217663" variation 785 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="t" /db_xref="dbSNP:373952633" variation 801 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="t" /db_xref="dbSNP:373433353" variation 854 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="g" /db_xref="dbSNP:201297341" variation 956 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="t" /db_xref="dbSNP:147174389" variation 974 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="c" /db_xref="dbSNP:376325506" variation 1013 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="c" /db_xref="dbSNP:141288498" variation 1047 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="g" /replace="t" /db_xref="dbSNP:202241409" variation 1094 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="g" /db_xref="dbSNP:371230694" variation 1135 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="g" /db_xref="dbSNP:374139731" variation 1155 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="g" /db_xref="dbSNP:199832736" variation 1227 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="g" /db_xref="dbSNP:1051929" variation 1247 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="t" /db_xref="dbSNP:201412033" variation 1249 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="t" /db_xref="dbSNP:368898563" variation 1259 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="g" /db_xref="dbSNP:372195235" variation 1282 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="c" /db_xref="dbSNP:374967073" variation 1299 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="t" /db_xref="dbSNP:200410001" variation 1305 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="g" /db_xref="dbSNP:199829552" variation 1313 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="g" /db_xref="dbSNP:146292581" variation 1337 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="g" /db_xref="dbSNP:374894451" variation 1358 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="g" /replace="t" /db_xref="dbSNP:368978061" variation 1399 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="t" /db_xref="dbSNP:374462578" variation 1430 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="g" /db_xref="dbSNP:200844846" variation 1484 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="g" /db_xref="dbSNP:201134562" variation 1535..1536 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="" /replace="a" /db_xref="dbSNP:71409074" variation 1540 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="t" /db_xref="dbSNP:369109077" variation 1584 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="t" /db_xref="dbSNP:75081700" variation 1608 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="g" /db_xref="dbSNP:369602867" variation 1630 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="g" /db_xref="dbSNP:35746949" variation 1656 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="g" /replace="t" /db_xref="dbSNP:112414246" variation 1657..1658 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="" /replace="ctt" /replace="tct" /db_xref="dbSNP:34952493" variation 1658..1659 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="" /replace="ttc" /db_xref="dbSNP:60794848" variation 1659..1660 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="" /replace="ttc" /db_xref="dbSNP:72050501" variation 1659 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="t" /db_xref="dbSNP:186345984" variation 1733 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="t" /db_xref="dbSNP:1051928" variation 1734 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="t" /db_xref="dbSNP:1051927" variation 1738 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="g" /db_xref="dbSNP:143449156" variation 1784 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="t" /db_xref="dbSNP:711830" variation 1789 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="c" /db_xref="dbSNP:75690576" variation 1901 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="g" /replace="t" /db_xref="dbSNP:148367105" variation 2036 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="g" /replace="t" /db_xref="dbSNP:376448993" variation 2132 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="g" /db_xref="dbSNP:182114564" variation 2184..2185 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="g" /replace="t" /db_xref="dbSNP:2857536" variation 2184 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="g" /replace="t" /db_xref="dbSNP:966800" variation 2193 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="c" /replace="t" /db_xref="dbSNP:115537830" variation 2196 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="g" /db_xref="dbSNP:141586867" polyA_signal 2280..2285 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" polyA_site 2299 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /experiment="experimental evidence, no additional details recorded" variation 2300 /gene="HOXD3" /gene_synonym="Hox-4.1; HOX1D; HOX4; HOX4A" /replace="a" /replace="g" /db_xref="dbSNP:966801" ORIGIN
gcctccacagatatcaaaagaaacctgaagagcctacaaaaaaaaaagagataaagacaaaattcaagaaaacacacacatacataattgtggtcacctggagcctgggggccggcccagctctctcaggattcagcagacattggaggtggcagtgaaggatacagtggtagtcaatgttatttgagcagggtcagcaggccctggagcttcctgagtgcacaatgcagaaggctgcttactatgaaaacccaggactgtttggaggctatggctacagcaaaactacggacacttacggctacagcaccccccaccagccctacccaccccctgctgctgccagctccctggacactgactatccaggttctgcctgctccatccagagctctgcccctctgagagccccagcccacaaaggagctgaactcaatggcagctgcatgcggccgggcactgggaacagccagggtgggggtggtggcagccagcctcctggtctgaactcagagcagcagccaccacaaccccctcctccaccaccgaccctgcccccatcttcacccaccaatcctggaggtggagtgcctgccaagaagcccaaaggtgggcccaatgcttctagctcctcagccaccatcagcaagcagatcttcccctggatgaaagagtctcgacagaactccaagcagaagaacagctgtgccactgcaggagagagctgcgaggacaagagcccgccaggcccagcatccaagcgggtacgcacggcatacacgagcgcgcagctggtggaattggaaaaggaattccacttcaaccgctacttgtgccggccgcgccgcgtggagatggccaacctgctgaatctcacggaacgccagatcaagatctggttccagaaccggcgcatgaagtacaagaaggaccagaaggccaagggcatcctgcactcgccggctagccagtcccctgagcgcagcccaccgctcggcggcgccgctggccacgtggcctactccggccagctgccgccagtgcccggcctggcctacgacgcgccctcgccgcctgctttcgccaaatcacagcccaatatgtacggcctggccgcctacacggcgccactcagcagctgcctgccacaacagaagcgctacgcagcgccggagttcgagccccatcccatggcgagcaacggcggcggcttcgccagcgccaacttgcagggcagcccggtgtacgtgggcggcaacttcgtcgagtccatggcgcccgcgtccgggcctgtcttcaacctgggccacctctcgcacccgtcgtcggccagcgtggactacagttgcgccgcgcagattccaggcaaccaccaccatggaccttgcgaccctcatcccacctacacagatctctcggcccaccactcgtctcagggacgactgccggaggctcccaaactgacgcatctgtagcggccgccgccagcccgaactcgcggcaaaattacctctcttgctgtagtggtggggtagagggtggggcccgcggggcagttcgggaacccccttccccgctcttgccctgccgccgcctcccgggtctcaggcctccagcggcggaggcgcaggcgaccgggcctcccctccatgggcgtcctttgggtgactcgccataaatcagccgcaaggatccttccctgtaaatttgacagtgccacatactgcggaccaagggactccaatctggtaatggtgtcccaaaggtaagtctgagacccatcagcggcgcgccctgcagagggaccagagcttggagagtcttgggcctggcccgcgtctagcttagtttcagagaccttaatttatattctccttcctgtgccgtaaggattgcatcggactaaactatctgtatttattatttgaagcgagtcatttcgttccctgattatttatccttgtctgaatgtatttatgtgtatatttgtagatttatccagccgagcttaggaattcgcttccaggccgtgggggccacatttcacctccttagtccccctggtctgaactagttgagagagtagttttgaacagtcgtaaccgtggctggtgtttgtagttgacataaaggattaagaccgcaaattgtccttcatgggtagagtcaggaagcccggtggcgtggcacaacacactttggtcatttctcaaaaaccacagtcctcaccacagtttattgatttcaaattgtctggtactattggaacaaatatttagaataaaaaaatttcccagtcaaaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:3232 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: IEA GeneID:3232 -> Molecular function: GO:0005515 [protein binding] evidence: IPI GeneID:3232 -> Molecular function: GO:0043565 [sequence-specific DNA binding] evidence: IEA GeneID:3232 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IMP GeneID:3232 -> Biological process: GO:0007160 [cell-matrix adhesion] evidence: IDA GeneID:3232 -> Biological process: GO:0007219 [Notch signaling pathway] evidence: IMP GeneID:3232 -> Biological process: GO:0009952 [anterior/posterior pattern specification] evidence: ISS GeneID:3232 -> Biological process: GO:0010628 [positive regulation of gene expression] evidence: IMP GeneID:3232 -> Biological process: GO:0021615 [glossopharyngeal nerve morphogenesis] evidence: IEA GeneID:3232 -> Biological process: GO:0030878 [thyroid gland development] evidence: ISS GeneID:3232 -> Biological process: GO:0045666 [positive regulation of neuron differentiation] evidence: ISS GeneID:3232 -> Biological process: GO:0048704 [embryonic skeletal system morphogenesis] evidence: ISS GeneID:3232 -> Biological process: GO:0051216 [cartilage development] evidence: ISS GeneID:3232 -> Cellular component: GO:0005634 [nucleus] evidence: IC
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