2025-05-09 19:12:12, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_002148 1814 bp mRNA linear PRI 05-MAY-2013 DEFINITION Homo sapiens homeobox D10 (HOXD10), mRNA. ACCESSION NM_002148 VERSION NM_002148.3 GI:85380098 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 1814) AUTHORS Liu,Z., Zhu,J., Cao,H., Ren,H. and Fang,X. TITLE miR-10b promotes cell invasion through RhoC-AKT signaling pathway by targeting HOXD10 in gastric cancer JOURNAL Int. J. Oncol. 40 (5), 1553-1560 (2012) PUBMED 22293682 REMARK GeneRIF: Suggest that miR-10b can stimulate the upregulation of RhoC and AKT phosphorylation through targeting HOXD10, thus promoting cell invasion in gastric tumors. REFERENCE 2 (bases 1 to 1814) AUTHORS Wang,L., Chen,S., Xue,M., Zhong,J., Wang,X., Gan,L., Lam,E.K., Liu,X., Zhang,J., Zhou,T., Yu,J., Jin,H. and Si,J. TITLE Homeobox D10 gene, a candidate tumor suppressor, is downregulated through promoter hypermethylation and associated with gastric carcinogenesis JOURNAL Mol. Med. 18, 389-400 (2012) PUBMED 22160393 REMARK GeneRIF: HoxD10 potentially functions as a tumor suppressor that is inactivated through promoter hypermethylation in gastric cancer. Publication Status: Online-Only REFERENCE 3 (bases 1 to 1814) AUTHORS Sun,L., Yan,W., Wang,Y., Sun,G., Luo,H., Zhang,J., Wang,X., You,Y., Yang,Z. and Liu,N. TITLE MicroRNA-10b induces glioma cell invasion by modulating MMP-14 and uPAR expression via HOXD10 JOURNAL Brain Res. 1389, 9-18 (2011) PUBMED 21419107 REMARK GeneRIF: miR-10b induced glioma cell invasion by modulating tumor invasion factors MMP-14 and uPAR expression via the direct target HOXD10 REFERENCE 4 (bases 1 to 1814) AUTHORS Yerges,L.M., Klei,L., Cauley,J.A., Roeder,K., Kammerer,C.M., Moffett,S.P., Ensrud,K.E., Nestlerode,C.S., Marshall,L.M., Hoffman,A.R., Lewis,C., Lang,T.F., Barrett-Connor,E., Ferrell,R.E., Orwoll,E.S. and Zmuda,J.M. CONSRTM MrOS Research Group TITLE High-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older men JOURNAL J. Bone Miner. Res. 24 (12), 2039-2049 (2009) PUBMED 19453261 REMARK GeneRIF: Observational study of gene-disease association. (HuGE Navigator) REFERENCE 5 (bases 1 to 1814) AUTHORS Reddy,S.D., Ohshiro,K., Rayala,S.K. and Kumar,R. TITLE MicroRNA-7, a homeobox D10 target, inhibits p21-activated kinase 1 and regulates its functions JOURNAL Cancer Res. 68 (20), 8195-8200 (2008) PUBMED 18922890 REMARK GeneRIF: Pak1 is a target of miR-7 and that HoxD10 plays a regulatory role in modifying the expression of miR-7. REFERENCE 6 (bases 1 to 1814) AUTHORS Tabin,C.J. TITLE Why we have (only) five fingers per hand: hox genes and the evolution of paired limbs JOURNAL Development 116 (2), 289-296 (1992) PUBMED 1363084 REMARK Review article REFERENCE 7 (bases 1 to 1814) AUTHORS Redline,R.W., Williams,A.J., Patterson,P. and Collins,T. TITLE Human HOX4E: a gene strongly expressed in the adult male and female urogenital tracts JOURNAL Genomics 13 (2), 425-430 (1992) PUBMED 1351871 REFERENCE 8 (bases 1 to 1814) AUTHORS Zappavigna,V., Renucci,A., Izpisua-Belmonte,J.C., Urier,G., Peschle,C. and Duboule,D. TITLE HOX4 genes encode transcription factors with potential auto- and cross-regulatory capacities JOURNAL EMBO J. 10 (13), 4177-4187 (1991) PUBMED 1756725 REFERENCE 9 (bases 1 to 1814) AUTHORS Peverali,F.A., D'Esposito,M., Acampora,D., Bunone,G., Negri,M., Faiella,A., Stornaiuolo,A., Pannese,M., Migliaccio,E., Simeone,A. et al. TITLE Expression of HOX homeogenes in human neuroblastoma cell culture lines JOURNAL Differentiation 45 (1), 61-69 (1990) PUBMED 1981366 REFERENCE 10 (bases 1 to 1814) 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 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AL526269.3, BC069619.1, BX114645.1, AW243295.1, AW299531.1 and AA653427.1. This sequence is a reference standard in the RefSeqGene project. On Jan 19, 2006 this sequence version replaced gi:23510365. Summary: This gene is a member of the Abd-B homeobox family and encodes a protein with a homeobox DNA-binding domain. It is included in a cluster of homeobox D genes located on chromosome 2. The encoded nuclear protein functions as a sequence-specific transcription factor that is expressed in the developing limb buds and is involved in differentiation and limb development. Mutations in this gene have been associated with Wilm's tumor and congenital vertical talus (also known as 'rocker-bottom foot' deformity or congenital convex pes valgus) and/or a foot deformity resembling that seen in Charcot-Marie-Tooth disease. [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 :: BC069619.1, X59373.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025084, ERS025085 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-20 AL526269.3 1-20 21-1164 BC069619.1 1-1144 1165-1204 BX114645.1 533-572 1205-1560 AW243295.1 1-356 c 1561-1766 AW299531.1 33-238 c 1767-1814 AA653427.1 17-64 c FEATURES Location/Qualifiers source 1..1814 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="2" /map="2q31.1" gene 1..1814 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /note="homeobox D10" /db_xref="GeneID:3236" /db_xref="HGNC:5133" /db_xref="HPRD:00867" /db_xref="MIM:142984" exon 1..815 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /inference="alignment:Splign:1.39.8" STS 21..1164 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /db_xref="UniSTS:481578" STS 22..1137 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /db_xref="UniSTS:481921" STS 44..1181 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /db_xref="UniSTS:486644" variation 58 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="a" /replace="t" /db_xref="dbSNP:202083006" variation 68 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="a" /replace="g" /db_xref="dbSNP:367831798" CDS 71..1093 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /note="homeo box D10; homeo box 4D; homeobox protein Hox-4D; homeobox protein Hox-4E" /codon_start=1 /product="homeobox protein Hox-D10" /protein_id="NP_002139.2" /db_xref="GI:23510366" /db_xref="CCDS:CCDS2266.1" /db_xref="GeneID:3236" /db_xref="HGNC:5133" /db_xref="HPRD:00867" /db_xref="MIM:142984" /translation="
MSFPNSSPAANTFLVDSLISACRSDSFYSSSASMYMPPPSADMGTYGMQTCGLLPSLAKREVNHQNMGMNVHPYIPQVDSWTDPNRSCRIEQPVTQQVPTCSFTTNIKEESNCCMYSDKRNKLISAEVPSYQRLVPESCPVENPEVPVPGYFRLSQTYATGKTQEYNNSPEGSSTVMLQLNPRGAAKPQLSAAQLQMEKKMNEPVSGQEPTKVSQVESPEAKGGLPEERSCLAEVSVSSPEVQEKESKEEIKSDTPTSNWLTAKSGRKKRCPYTKHQTLELEKEFLFNMYLTRERRLEISKSVNLTDRQVKIWFQNRRMKLKKMSRENRIRELTANLTFS
" misc_feature 869..1045 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /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(869..883,887..889,938..940,956..958,995..997, 1001..1006,1013..1018,1022..1030,1034..1039) /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /note="DNA binding site [nucleotide binding]" /db_xref="CDD:28970" misc_feature order(875..877,884..886,1004..1006,1013..1018,1025..1027) /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /note="specific DNA base contacts [nucleotide binding]; other site" /db_xref="CDD:28970" variation 133 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="c" /replace="t" /db_xref="dbSNP:375832062" variation 170 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="a" /replace="g" /db_xref="dbSNP:373631327" variation 200 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="a" /replace="g" /db_xref="dbSNP:145541578" variation 201 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="c" /replace="g" /db_xref="dbSNP:144658174" variation 207 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="a" /replace="g" /db_xref="dbSNP:375742820" variation 229 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="g" /replace="t" /db_xref="dbSNP:199871119" variation 240 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="c" /replace="t" /db_xref="dbSNP:201449517" variation 244 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="c" /replace="g" /db_xref="dbSNP:148512736" variation 325 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="c" /replace="t" /db_xref="dbSNP:140907245" variation 336 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="a" /replace="g" /db_xref="dbSNP:374700658" variation 347 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="c" /replace="g" /db_xref="dbSNP:144865820" variation 372 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="a" /replace="g" /db_xref="dbSNP:139302218" variation 433 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="c" /replace="t" /db_xref="dbSNP:7604313" variation 442 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="g" /replace="t" /db_xref="dbSNP:149038150" variation 450 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="a" /replace="g" /db_xref="dbSNP:146704863" variation 456 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="c" /replace="t" /db_xref="dbSNP:372128583" variation 490 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="c" /replace="g" /db_xref="dbSNP:375702128" variation 535 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="c" /replace="t" /db_xref="dbSNP:141770128" variation 540 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="c" /replace="g" /db_xref="dbSNP:187717603" variation 551 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="g" /replace="t" /db_xref="dbSNP:370540453" variation 553 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="a" /replace="g" /db_xref="dbSNP:367895774" variation 568 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="c" /replace="t" /db_xref="dbSNP:375466143" variation 596 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="c" /replace="g" /db_xref="dbSNP:372134472" variation 631 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="a" /replace="g" /db_xref="dbSNP:143870330" variation 634 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="c" /replace="g" /db_xref="dbSNP:2593777" variation 635 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="c" /replace="g" /db_xref="dbSNP:2593778" variation 657 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="a" /replace="g" /db_xref="dbSNP:147270324" variation 676 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="c" /replace="g" /db_xref="dbSNP:143111542" variation 689 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="g" /replace="t" /db_xref="dbSNP:148563899" variation 731 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="g" /replace="t" /db_xref="dbSNP:201752392" variation 740 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="c" /replace="g" /db_xref="dbSNP:377417077" variation 748 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="c" /replace="g" /db_xref="dbSNP:151123199" STS 760..906 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /standard_name="Hoxd10" /db_xref="UniSTS:536667" variation 768 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="a" /replace="c" /db_xref="dbSNP:112907565" variation 800 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="a" /replace="g" /db_xref="dbSNP:370776975" exon 816..1804 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /inference="alignment:Splign:1.39.8" variation 838 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="a" /replace="c" /db_xref="dbSNP:61740491" STS 844..1057 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /standard_name="Hoxd9" /db_xref="UniSTS:143400" variation 851 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="c" /replace="t" /db_xref="dbSNP:201987368" variation 892 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="c" /replace="t" /db_xref="dbSNP:200874129" variation 977 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="a" /replace="g" /db_xref="dbSNP:373028650" variation 988 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="c" /replace="t" /db_xref="dbSNP:376251268" variation 1001 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="a" /replace="g" /db_xref="dbSNP:145367242" variation 1012 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="a" /replace="t" /db_xref="dbSNP:78466921" variation 1013 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="a" /replace="c" /db_xref="dbSNP:75752744" variation 1026 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="a" /replace="t" /db_xref="dbSNP:104893634" variation 1057 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="c" /replace="g" /db_xref="dbSNP:33913965" variation 1068 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="c" /replace="t" /db_xref="dbSNP:144160937" variation 1095 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="c" /replace="t" /db_xref="dbSNP:116807022" variation 1119 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="a" /replace="t" /db_xref="dbSNP:375226686" variation 1140 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="g" /replace="t" /db_xref="dbSNP:114746583" variation 1148 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="g" /replace="t" /db_xref="dbSNP:61070787" variation 1199 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="c" /replace="t" /db_xref="dbSNP:374054273" STS 1277..1379 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /standard_name="GDB:192883" /db_xref="UniSTS:155728" variation 1297..1298 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="" /replace="tatata" /db_xref="dbSNP:71409068" variation 1298..1299 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="" /replace="ta" /replace="tata" /replace="tatatatatatatatata" /replace="tatatatatatatatatatatata" /db_xref="dbSNP:67520913" variation 1307..1308 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="" /replace="atatatatat" /db_xref="dbSNP:71894275" variation 1309..1310 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="" /replace="atatat" /db_xref="dbSNP:67337589" variation 1312 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="g" /replace="t" /db_xref="dbSNP:113753022" variation 1315..1328 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="" /replace="atatatatatataa" /db_xref="dbSNP:143734503" variation 1317..1328 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="" /replace="atatatatataa" /db_xref="dbSNP:200449718" variation 1317..1318 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="" /replace="atatat" /db_xref="dbSNP:66948465" variation 1319..1320 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="" /replace="atatat" /db_xref="dbSNP:72269703" variation 1320..1321 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="" /replace="tatata" /db_xref="dbSNP:71871871" variation 1327..1328 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="" /replace="tatata" /replace="tatatatatatatata" /replace="tatatatatatatatata" /db_xref="dbSNP:6147035" variation 1328..1329 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="" /replace="tatatatatatatata" /replace="tatatatatatatatata" /replace="tatatatatatatatatatatata" /db_xref="dbSNP:33990556" variation 1328 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="a" /replace="t" /db_xref="dbSNP:76652386" variation 1372 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="a" /replace="g" /db_xref="dbSNP:150556295" variation 1444 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="g" /replace="t" /db_xref="dbSNP:189196087" variation 1499 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="c" /replace="t" /db_xref="dbSNP:180928138" variation 1505..1506 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="" /replace="c" /db_xref="dbSNP:35586190" variation 1546..1547 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="" /replace="a" /db_xref="dbSNP:34995639" variation 1560..1561 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="" /replace="a" /db_xref="dbSNP:113041382" variation 1588 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="a" /replace="t" /db_xref="dbSNP:13403839" variation 1669 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="a" /replace="g" /db_xref="dbSNP:184375199" variation 1673 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="a" /replace="g" /db_xref="dbSNP:78395870" variation 1678 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="c" /replace="t" /db_xref="dbSNP:72923454" polyA_signal 1782..1787 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" variation 1793 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" /replace="c" /replace="g" /db_xref="dbSNP:189753416" polyA_site 1804 /gene="HOXD10" /gene_synonym="Hox-4.4; HOX4; HOX4D; HOX4E" ORIGIN
cggggaatgttttcctagagatgtcagcctacaaaggacacaatctctcttcttcaaattcttccccaaaatgtcctttcccaacagctctcctgctgctaatacttttttagtagattccttgatcagtgcctgcaggagtgacagtttttattccagcagcgccagcatgtacatgccaccacctagcgcagacatggggacctatggaatgcaaacctgtggactgctcccgtctctggccaaaagagaagtgaaccaccaaaatatgggtatgaatgtgcatccttatatacctcaagtagacagttggacagatccgaacagatcttgtcgaatagagcaacctgttacacagcaagtccccacttgctccttcaccaccaacattaaggaagaatccaattgctgcatgtattctgataagcgcaacaaactcatttcggccgaggtcccttcgtaccagaggctggtccctgagtcttgtcccgttgagaaccctgaggttcccgtccctggatattttagactgagtcagacctacgccaccgggaaaacccaagagtacaataatagccccgaaggcagctccactgtcatgctccagctcaaccctcgtggcgcggccaagccgcagctctccgctgcccagctgcagatggaaaagaagatgaacgagcccgtgagcggccaggagcccaccaaagtctcccaggtggagagccccgaggccaaaggcggccttcccgaagagaggagctgcctggctgaggtctccgtgtccagtcccgaagtgcaggagaaggaaagcaaagaggaaatcaagtctgatacaccaaccagcaattggctcactgcaaagagtggcagaaagaagaggtgcccttacactaagcaccaaacgctggaattagaaaaagagttcttgttcaatatgtacctcacccgcgagcgccgcctagagatcagtaagagcgttaacctcaccgacaggcaggtcaagatttggtttcaaaaccgccgaatgaaactcaagaagatgagccgagagaaccggatccgagaactgaccgccaacctcacgttttcttaggtctgaggccggtctgaggccggtcagaggccaggattggagagggggcaccgcgttccagggcccagtgctggaggactgggaaagcggaaacaaaaccttcaccgctctttgtttgttgttttgttgtattttgttttcctgctagaatgtgactttggggtcattatgttcgtgctgcaagtgatctgtaatccctatgagtatatatatatatatatatatatatatataaaaacttagcacgtgtaatttattattttttcatcgtaatgcagggtaactattattgcgcattttcatttgggtcttaacttattggaactgtagagcatccatccatccatccatccagcaatgtgactttttcatgtctttcctaacacaaaaggtctatgtgtgtggttagtccatgaactcatggcattttgaatacatccagtactttaaaaatgacatatatatttaaaaaaaaaagattaagaaaacccacaagttggagggagggggacttaaaaagcacattacaatgtatcttttcacaaatgaatttagcagttgtccttggtgagatgggatattggcgatttatgccttgtagcctttcccttgtggtgcatctgtggtttggtagaagtacaacagcaacctgtcctttctgtgcatgttctggtcgcatgtataatgcaataaactctggaaatgagttcaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:3236 -> Molecular function: GO:0003682 [chromatin binding] evidence: IEA GeneID:3236 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: IEA GeneID:3236 -> Molecular function: GO:0043565 [sequence-specific DNA binding] evidence: IEA GeneID:3236 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IEA GeneID:3236 -> Biological process: GO:0007519 [skeletal muscle tissue development] evidence: IEA GeneID:3236 -> Biological process: GO:0008344 [adult locomotory behavior] evidence: IEA GeneID:3236 -> Biological process: GO:0009952 [anterior/posterior pattern specification] evidence: IEA GeneID:3236 -> Biological process: GO:0009954 [proximal/distal pattern formation] evidence: IEA GeneID:3236 -> Biological process: GO:0021520 [spinal cord motor neuron cell fate specification] evidence: IEA GeneID:3236 -> Biological process: GO:0030326 [embryonic limb morphogenesis] evidence: IEA GeneID:3236 -> Biological process: GO:0035136 [forelimb morphogenesis] evidence: IEA GeneID:3236 -> Biological process: GO:0035137 [hindlimb morphogenesis] evidence: IEA GeneID:3236 -> Biological process: GO:0045944 [positive regulation of transcription from RNA polymerase II promoter] evidence: IEA GeneID:3236 -> Biological process: GO:0048704 [embryonic skeletal system morphogenesis] evidence: IEA GeneID:3236 -> Biological process: GO:0048935 [peripheral nervous system neuron development] evidence: IEA GeneID:3236 -> Biological process: GO:0050905 [neuromuscular process] evidence: IEA GeneID:3236 -> Cellular component: GO:0005634 [nucleus] evidence: IEA
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