LOCUS       NM_017409               2017 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens homeobox C10 (HOXC10), mRNA.
ACCESSION   NM_017409
VERSION     NM_017409.3  GI:84043953
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 2017)
  AUTHORS   Hwang,J.H., Seok,O.S., Song,H.R., Jo,J.Y. and Lee,J.K.
  TITLE     HOXC10 as a potential marker for discriminating between amnion- and
            decidua-derived mesenchymal stem cells
  JOURNAL   Cloning Stem Cells 11 (2), 269-279 (2009)
   PUBMED   19522674
  REMARK    GeneRIF: Data demonstrate that HOXC10 is a gene that may
            discriminate between amnion-derived mesenchymal stem cells (MSCs)
            and decidua-derived MSCs.
REFERENCE   2  (bases 1 to 2017)
  AUTHORS   Zhai,Y., Kuick,R., Nan,B., Ota,I., Weiss,S.J., Trimble,C.L.,
            Fearon,E.R. and Cho,K.R.
  TITLE     Gene expression analysis of preinvasive and invasive cervical
            squamous cell carcinomas identifies HOXC10 as a key mediator of
            invasion
  JOURNAL   Cancer Res. 67 (21), 10163-10172 (2007)
   PUBMED   17974957
  REMARK    GeneRIF: Cervical cancer cells with high endogenous levels of
            HOXC10 were less invasive after short hairpin RNA-mediated
            knockdown of HOXC10 expression; findings support a key role for the
            HOXC10 homeobox protein in cervical cancer progression
REFERENCE   3  (bases 1 to 2017)
  AUTHORS   Gabellini,D., Colaluca,I.N., Vodermaier,H.C., Biamonti,G.,
            Giacca,M., Falaschi,A., Riva,S. and Peverali,F.A.
  TITLE     Early mitotic degradation of the homeoprotein HOXC10 is potentially
            linked to cell cycle progression
  JOURNAL   EMBO J. 22 (14), 3715-3724 (2003)
   PUBMED   12853486
  REMARK    GeneRIF: Early mitotic dedgradation of the homeoprotein HOXC10 is
            potentially linked to cell cycle progression.
REFERENCE   4  (bases 1 to 2017)
  AUTHORS   Kosaki,K., Kosaki,R., Suzuki,T., Yoshihashi,H., Takahashi,T.,
            Sasaki,K., Tomita,M., McGinnis,W. and Matsuo,N.
  TITLE     Complete mutation analysis panel of the 39 human HOX genes
  JOURNAL   Teratology 65 (2), 50-62 (2002)
   PUBMED   11857506
REFERENCE   5  (bases 1 to 2017)
  AUTHORS   Sandrock,B. and Egly,J.M.
  TITLE     A yeast four-hybrid system identifies Cdk-activating kinase as a
            regulator of the XPD helicase, a subunit of transcription factor
            IIH
  JOURNAL   J. Biol. Chem. 276 (38), 35328-35333 (2001)
   PUBMED   11445587
REFERENCE   6  (bases 1 to 2017)
  AUTHORS   de Stanchina,E., Gabellini,D., Norio,P., Giacca,M., Peverali,F.A.,
            Riva,S., Falaschi,A. and Biamonti,G.
  TITLE     Selection of homeotic proteins for binding to a human DNA
            replication origin
  JOURNAL   J. Mol. Biol. 299 (3), 667-680 (2000)
   PUBMED   10835276
REFERENCE   7  (bases 1 to 2017)
  AUTHORS   Flagiello,D., Gibaud,A., Dutrillaux,B., Poupon,M.F. and Malfoy,B.
  TITLE     Distinct patterns of all-trans retinoic acid dependent expression
            of HOXB and HOXC homeogenes in human embryonal and small-cell lung
            carcinoma cell lines
  JOURNAL   FEBS Lett. 415 (3), 263-267 (1997)
   PUBMED   9357979
REFERENCE   8  (bases 1 to 2017)
  AUTHORS   Apiou,F., Flagiello,D., Cillo,C., Malfoy,B., Poupon,M.F. and
            Dutrillaux,B.
  TITLE     Fine mapping of human HOX gene clusters
  JOURNAL   Cytogenet. Cell Genet. 73 (1-2), 114-115 (1996)
   PUBMED   8646877
REFERENCE   9  (bases 1 to 2017)
  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 2017)
  AUTHORS   Rabin,M., Ferguson-Smith,A., Hart,C.P. and Ruddle,F.H.
  TITLE     Cognate homeo-box loci mapped on homologous human and mouse
            chromosomes
  JOURNAL   Proc. Natl. Acad. Sci. U.S.A. 83 (23), 9104-9108 (1986)
   PUBMED   2878432
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from AL558161.3, BC001293.1 and
            AC012531.11.
            On Dec 29, 2005 this sequence version replaced gi:24497532.
            
            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, which are located on different
            chromosomes and consist of 9 to 11 genes arranged in tandem. This
            gene is one of several homeobox HOXC genes located in a cluster on
            chromosome 12. The protein level is controlled during cell
            differentiation and proliferation, which may indicate this protein
            has a role in origin activation. [provided by RefSeq, Jul 2008].
            
            ##Evidence-Data-START##
            Transcript exon combination :: BC001293.1, AF255675.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025081, ERS025084 [ECO:0000348]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-27                AL558161.3         1-27
            28-1396             BC001293.1         1-1369
            1397-1930           AC012531.11        127320-127853
            1931-2017           BC001293.1         1903-1989
FEATURES             Location/Qualifiers
     source          1..2017
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="12"
                     /map="12q13.3"
     gene            1..2017
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /note="homeobox C10"
                     /db_xref="GeneID:3226"
                     /db_xref="HGNC:5122"
                     /db_xref="HPRD:05710"
                     /db_xref="MIM:605560"
     exon            1..849
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /inference="alignment:Splign:1.39.8"
     variation       24
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:371779186"
     variation       28
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373914181"
     variation       37
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376865524"
     misc_feature    78..80
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /note="upstream in-frame stop codon"
     CDS             99..1127
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /note="homeo box C10; homeoprotein C10; homeobox protein
                     Hox-3I"
                     /codon_start=1
                     /product="homeobox protein Hox-C10"
                     /protein_id="NP_059105.2"
                     /db_xref="GI:24497533"
                     /db_xref="CCDS:CCDS8868.1"
                     /db_xref="GeneID:3226"
                     /db_xref="HGNC:5122"
                     /db_xref="HPRD:05710"
                     /db_xref="MIM:605560"
                     /translation="

MTCPRNVTPNSYAEPLAAPGGGERYSRSAGMYMQSGSDFNCGVMRGCGLAPSLSKRDEGSSPSLALNTYPSYLSQLDSWGDPKAAYRLEQPVGRPLSSCSYPPSVKEENVCCMYSAEKRAKSGPEAALYSHPLPESCLGEHEVPVPSYYRASPSYSALDKTPHCSGANDFEAPFEQRASLNPRAEHLESPQLGGKVSFPETPKSDSQTPSPNEIKTEQSLAGPKGSPSESEKERAKAADSSPDTSDNEAKEEIKAENTTGNWLTAKSGRKKRCPYTKHQTLELEKEFLFNMYLTRERRLEISKTINLTDRQVKIWFQNRRMKLKKMNRENRIRELTSNFNFT

"
     misc_feature    663..665
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (Q9NYD6.2); phosphorylation site"
     misc_feature    903..1079
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /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(903..917,921..923,972..974,990..992,1029..1031,
                     1035..1040,1047..1052,1056..1064,1068..1073)
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /note="DNA binding site [nucleotide binding]"
                     /db_xref="CDD:28970"
     misc_feature    order(909..911,918..920,1038..1040,1047..1052,1059..1061)
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /note="specific DNA base contacts [nucleotide binding];
                     other site"
                     /db_xref="CDD:28970"
     variation       104
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:199882722"
     variation       137
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:137861505"
     variation       169
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:375878835"
     variation       172
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:187240221"
     variation       176
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200965954"
     variation       206
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140615920"
     variation       208
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373393716"
     variation       234
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150474647"
     variation       260
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138287881"
     variation       265
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:149610444"
     variation       291
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:370825874"
     variation       297
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:146103441"
     variation       350
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:33927265"
     variation       376
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:141997209"
     variation       377
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146305379"
     variation       389
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:376524714"
     variation       390
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:146858845"
     variation       391
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371047038"
     variation       393
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373552672"
     variation       398
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367774632"
     variation       409
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:374991890"
     variation       439
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148499225"
     variation       482
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142714177"
     variation       484
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:199667628"
     variation       488
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150584004"
     variation       514
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:370406756"
     variation       524
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:139588733"
     variation       525
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374930821"
     variation       565
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:149717368"
     variation       568
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201002417"
     variation       569
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:36079135"
     variation       582
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368239850"
     variation       589
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372554206"
     variation       620
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:183454098"
     variation       651
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:34108563"
     variation       658
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:141237360"
     variation       665
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145093077"
     variation       725
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:4564384"
     variation       731
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201702051"
     variation       733
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:78002127"
     variation       773
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200824321"
     variation       811
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:375690973"
     variation       812
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369948426"
     variation       835
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:200566909"
     variation       839
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:202194945"
     exon            850..1960
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /inference="alignment:Splign:1.39.8"
     STS             870..1062
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /standard_name="Hoxc10"
                     /db_xref="UniSTS:143388"
     variation       899
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143836884"
     variation       918
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369261675"
     variation       942
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372806113"
     variation       980
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148164175"
     variation       981
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:147012647"
     variation       988
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199660010"
     variation       1079
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138069369"
     variation       1095
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377534424"
     variation       1105
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375042242"
     variation       1107
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369495069"
     variation       1117
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141068564"
     variation       1138
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373631729"
     variation       1144
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:370667773"
     variation       1154
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184950567"
     variation       1190
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:35616568"
     variation       1200..1201
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:200363226"
     variation       1233
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:189368208"
     variation       1274
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:181735048"
     variation       1360
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:77499918"
     variation       1397
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:4237810"
     variation       1517
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:186245023"
     variation       1520
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376953065"
     variation       1640
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1047660"
     variation       1705
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:192050838"
     variation       1780
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:74944702"
     variation       1782
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370073253"
     STS             1787..1913
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /standard_name="STS-N31842"
                     /db_xref="UniSTS:60726"
     variation       1822..1823
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace=""
                     /replace="cc"
                     /db_xref="dbSNP:3832829"
     variation       1822
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:76760728"
     variation       1824
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace=""
                     /replace="cc"
                     /db_xref="dbSNP:372515101"
     variation       1831
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:201873082"
     variation       1832..1833
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace=""
                     /replace="ca"
                     /db_xref="dbSNP:368914718"
     variation       1928..1929
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:140519231"
     variation       1929..1930
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:71697079"
     polyA_signal    1932..1937
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
     variation       1941
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:183362237"
     variation       1953
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141685098"
     polyA_site      1960
                     /gene="HOXC10"
                     /gene_synonym="HOX3I"
                     /experiment="experimental evidence, no additional details
                     recorded"
ORIGIN      

cctcccctccaaccgcgccccccctcccggatggggaaaaaaaaagatgtcagctcctccgctgtagtattgctccttaaaaacccctctctctgaaaatgacatgccctcgcaatgtaactccgaactcgtacgcggagcccttggctgcgcccggcggaggagagcgctatagccggagcgcaggcatgtatatgcagtctgggagtgacttcaattgcggggtgatgaggggctgcgggctcgcgccctcgctctccaagagggacgagggcagcagccccagcctcgccctcaacacctatccgtcctacctctcgcagctggactcctggggcgaccccaaagccgcctatcgcctggaacaacctgttggcaggccgctgtcctcctgctcctacccacctagtgtcaaggaggagaatgtctgctgcatgtacagcgcagagaagcgggcgaaaagtggccccgaggcagctctctactcccaccccttgccggagtcctgccttggggagcacgaggtacccgtgcccagctactaccgcgccagcccgagctactccgcgctggacaagacgccccactgttctggggccaacgacttcgaagcccctttcgagcagcgggccagtctcaacccgcgcgccgaacatctggaatcgcctcagctggggggcaaagtgagtttccctgagacccccaagtccgacagccagacccccagccccaatgaaatcaagacggagcagagcctggcgggccctaaagggagcccctcggagagcgaaaaggagagggccaaagctgccgactccagcccagacacctcggataacgaagcgaaagaggagataaaggcagaaaacaccacaggaaattggctgacagcaaagagcggaaggaagaagaggtgcccctatactaaacaccagacgctggaattggagaaagaatttctgttcaatatgtatttgacgcgagagcgccgcctggagattagcaagaccattaaccttacagacagacaagtcaaaatctggtttcaaaatcgcagaatgaaactcaagaaaatgaaccgagagaatcggatccgggaactgacctccaattttaatttcacctgagagcgcggcctctcctcctcccttcccgctccttcctctccccgcccctcctccctttgtgcctggtgatatatttttttttcctccctgagtataaatgcaatgcgactgcaaaaaaggcaaagacctcagactctccttccaagggacctgtggttcgtgctgcgaagatgcttccacttaaagcatgagaaatggggtgccgggatgtggggtgtggtgtgtgccctcatagatgggggtgggagtgtggctggtgtgtgtgtcaagccctcactcacccacgcactcacacacagcattctgttctccatgcaaagttaagatcgaatccatccgcttgtaggggaaaaaaaggaaaaaaattaaccagagagggtctgtaatctcgcagagcacaggcagaatcgttccttccttgctgcatttcctccttagactaatagacgttttggaaagttcggctagtgttcgtgtgtttgtcgtagcacccagagcctccaccaaaccctctccatgtctttacctcccagtcgctctaagaatctgcttgaagtctcgtatttgtactgctttctgcttttctcccacccctcctagcacccccacatcccccatctagtaacatctcagaaatttcatccagaggaacaaaaaaattaaaaatagaacatagcaaagcaaagacagaatgcccccccccccaaatattgtcctgtccctgtctgggagttgtgttatttaaagatattctgtatgttgtatcttttgcatgtagcttccttaatggagaaaaaaaaacctaataaatttccagaatcataatcctcaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaa

//

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:3226 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: IEA
            GeneID:3226 -> Molecular function: GO:0043565 [sequence-specific DNA binding] evidence: IEA
            GeneID:3226 -> Biological process: GO:0001501 [skeletal system development] evidence: IEA
            GeneID:3226 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IEA
            GeneID:3226 -> Biological process: GO:0008284 [positive regulation of cell proliferation] evidence: TAS
            GeneID:3226 -> Biological process: GO:0009952 [anterior/posterior pattern specification] evidence: IEA
            GeneID:3226 -> Biological process: GO:0009954 [proximal/distal pattern formation] evidence: IEA
            GeneID:3226 -> Biological process: GO:0021520 [spinal cord motor neuron cell fate specification] evidence: IEA
            GeneID:3226 -> Biological process: GO:0030326 [embryonic limb morphogenesis] evidence: IEA
            GeneID:3226 -> Biological process: GO:0050905 [neuromuscular process] evidence: IEA
            GeneID:3226 -> Cellular component: GO:0019907 [cyclin-dependent protein kinase activating kinase holoenzyme complex] evidence: IDA