LOCUS       NM_001199746            2596 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens homeobox D8 (HOXD8), transcript variant 2, mRNA.
ACCESSION   NM_001199746
VERSION     NM_001199746.1  GI:315075339
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 2596)
  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   2  (bases 1 to 2596)
  AUTHORS   Harada,K., Yamazaki,T., Iwata,C., Yoshimatsu,Y., Sase,H.,
            Mishima,K., Morishita,Y., Hirashima,M., Oike,Y., Suda,T., Miura,N.,
            Watabe,T. and Miyazono,K.
  TITLE     Identification of targets of Prox1 during in vitro vascular
            differentiation from embryonic stem cells: functional roles of
            HoxD8 in lymphangiogenesis
  JOURNAL   J. Cell. Sci. 122 (PT 21), 3923-3930 (2009)
   PUBMED   19825936
  REMARK    GeneRIF: Prox1 and HoxD8 play important roles in the maturation and
            maintenance of lymphatic vessels.
REFERENCE   3  (bases 1 to 2596)
  AUTHORS   Goodman,F.R.
  TITLE     Limb malformations and the human HOX genes
  JOURNAL   Am. J. Med. Genet. 112 (3), 256-265 (2002)
   PUBMED   12357469
  REMARK    Review article
REFERENCE   4  (bases 1 to 2596)
  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 2596)
  AUTHORS   Limongi,M.Z., Pelliccia,F., Gaddini,L. and Rocchi,A.
  TITLE     Clustering of two fragile sites and seven homeobox genes in human
            chromosome region 2q31-->q32.1
  JOURNAL   Cytogenet. Cell Genet. 90 (1-2), 151-153 (2000)
   PUBMED   11060466
REFERENCE   6  (bases 1 to 2596)
  AUTHORS   Manohar,C.F., Salwen,H.R., Furtado,M.R. and Cohn,S.L.
  TITLE     Up-regulation of HOXC6, HOXD1, and HOXD8 homeobox gene expression
            in human neuroblastoma cells following chemical induction of
            differentiation
  JOURNAL   Tumour Biol. 17 (1), 34-47 (1996)
   PUBMED   7501971
REFERENCE   7  (bases 1 to 2596)
  AUTHORS   Guazzi,S., Lonigro,R., Pintonello,L., Boncinelli,E., Di Lauro,R.
            and Mavilio,F.
  TITLE     The thyroid transcription factor-1 gene is a candidate target for
            regulation by Hox proteins
  JOURNAL   EMBO J. 13 (14), 3339-3347 (1994)
   PUBMED   7913891
REFERENCE   8  (bases 1 to 2596)
  AUTHORS   Rosen,D.R. and Brown,R.H. Jr.
  TITLE     Dinucleotide repeat polymorphism in the HOX4E locus
  JOURNAL   Hum. Mol. Genet. 2 (5), 617 (1993)
   PUBMED   8100165
REFERENCE   9  (bases 1 to 2596)
  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   10 (bases 1 to 2596)
  AUTHORS   Oliver,G., Sidell,N., Fiske,W., Heinzmann,C., Mohandas,T.,
            Sparkes,R.S. and De Robertis,E.M.
  TITLE     Complementary homeo protein gradients in developing limb buds
  JOURNAL   Genes Dev. 3 (5), 641-650 (1989)
   PUBMED   2568311
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from AC009336.13, BC038709.1 and
            AW140108.1.
            
            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 in a cluster on
            chromosome 2. Deletions that remove the entire HOXD gene cluster or
            the 5' end of this cluster have been associated with severe limb
            and genital abnormalities. In addition to effects during
            embryogenesis, this particular gene may also play a role in adult
            urogenital tract function. Alternate splicing results in multiple
            transcript variants.[provided by RefSeq, Dec 2010].
            
            Transcript Variant: This variant (2) uses an alternate in-frame
            splice site in the 3' coding region, compared to variant 1. This
            results in a shorter protein (isoform 2), compared to isoform 1.
            
            Sequence Note: This RefSeq record was created from transcript and
            genomic sequence data to make the sequence consistent with the
            reference genome assembly. The genomic coordinates used for the
            transcript record were based on transcript alignments.
            
            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 :: BC038709.1, BI764317.1 [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
            1-150               AC009336.13        113729-113878
            151-1904            BC038709.1         1-1754
            1905-2122           AC009336.13        116009-116226
            2123-2596           AW140108.1         1-474               c
FEATURES             Location/Qualifiers
     source          1..2596
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="2"
                     /map="2q31.1"
     gene            1..2596
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /note="homeobox D8"
                     /db_xref="GeneID:3234"
                     /db_xref="HGNC:5139"
                     /db_xref="MIM:142985"
     exon            1..1204
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /inference="alignment:Splign:1.39.8"
     variation       125
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:13033005"
     variation       156
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:847163"
     variation       261
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141068157"
     variation       272
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:847162"
     variation       323
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:7580355"
     misc_feature    499..501
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /note="upstream in-frame stop codon"
     CDS             628..1497
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /note="isoform 2 is encoded by transcript variant 2; homeo
                     box D8; homeobox protein 5.4; homeo box 4E; homeobox
                     protein Hox-D8; Hox-4.5; homeobox protein Hox-4E; homeobox
                     protein Hox-5.4"
                     /codon_start=1
                     /product="homeobox protein Hox-D8 isoform 2"
                     /protein_id="NP_001186675.1"
                     /db_xref="GI:315075340"
                     /db_xref="CCDS:CCDS56148.1"
                     /db_xref="GeneID:3234"
                     /db_xref="HGNC:5139"
                     /db_xref="MIM:142985"
                     /translation="

MSSYFVNPLYSKYKAAAAAAAAAGEAINPTYYDCHFAPEVGGRHAAAAAALQLYGNSAAGFPHAPPQAHAHPHPSPPPSGTGCGGREGRGQEYFHPGGGSPAAAYQAAPPPPPHPPPPPPPPPCGGIACHGEPAKFYGYDNLQRQPIFTTQQEAELVQYPDCKSSSGNIGEDPDHLNQSSSPSQMFPWMRPQAPGRRRGRQTYSRFQTLELEKEFLFNPYLTRKRRIEVSHALALTERQVKIWFQNRRMKWKKENNKDKFPVSRQEVKDGETKKEAQELEEDRAEGLTN

"
     misc_feature    1231..1392
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /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(1231..1233,1351..1353,1360..1365,1372..1374)
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /note="specific DNA base contacts [nucleotide binding];
                     other site"
                     /db_xref="CDD:28970"
     misc_feature    order(1234..1236,1285..1287,1303..1305,1342..1344,
                     1348..1353,1360..1365,1369..1377,1381..1386)
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /note="DNA binding site [nucleotide binding]"
                     /db_xref="CDD:28970"
     variation       679
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:192755857"
     variation       697
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace=""
                     /replace="cgg"
                     /db_xref="dbSNP:76009715"
     variation       795
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:7580746"
     variation       918
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150245338"
     variation       923
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:372539818"
     variation       938
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375776277"
     variation       954
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:369342903"
     variation       966
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:200396175"
     variation       985
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376804387"
     variation       995
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:371353708"
     variation       1011
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201371125"
     variation       1017
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:138844525"
     STS             1019..1126
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /standard_name="Hoxd8"
                     /db_xref="UniSTS:536673"
     variation       1023
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:149731656"
     variation       1038
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145566116"
     variation       1045
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:370947951"
     variation       1092
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147014120"
     variation       1108
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:374010247"
     variation       1119
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377728786"
     variation       1140
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:3765049"
     variation       1152
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148123943"
     variation       1167
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:138972805"
     variation       1187
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142220242"
     variation       1194
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371171284"
     STS             1201..1326
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /standard_name="RH18089"
                     /db_xref="UniSTS:47553"
     exon            1205..2580
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /inference="alignment:Splign:1.39.8"
     variation       1216
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:199871239"
     variation       1294
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375411869"
     variation       1306
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139078975"
     variation       1309
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199631106"
     variation       1349
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:200630630"
     variation       1357
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201900185"
     variation       1366
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201072995"
     variation       1400
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:143950622"
     variation       1431
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371256205"
     variation       1432
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:147814791"
     variation       1435
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:113257910"
     variation       1438
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201690967"
     variation       1449
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:375876165"
     STS             1485..2026
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /standard_name="HOXD8_4104"
                     /db_xref="UniSTS:462900"
     variation       1491
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:191736932"
     variation       1493
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:75818878"
     variation       1516
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:184720506"
     variation       1554
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:145623178"
     variation       1664
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:138242849"
     variation       1721
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:189097507"
     variation       1733
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149532657"
     variation       1789
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:181506551"
     variation       1907
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:201637028"
     variation       1945
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:144187682"
     STS             1991..2154
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /standard_name="SHGC-52388"
                     /db_xref="UniSTS:64729"
     polyA_signal    2210..2215
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
     polyA_site      2236
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
     variation       2344
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:111760092"
     variation       2432
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112559843"
     variation       2511
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:148663631"
     polyA_signal    2559..2564
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
     variation       2571
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:190277759"
     polyA_site      2580
                     /gene="HOXD8"
                     /gene_synonym="HOX4; HOX4E; HOX5.4"
ORIGIN      

tccgtgcagtgctgtggtgcgaaaatgcctcgccggtgcgcaccgggtcggcagcctcggcggcgggggcgagattggcgggaggggggcgcggggggggcgcggtaagaggtggcggcgggcagagggtgttttttttcttttccctccagagccggggtttgtaaaccgaggccagagtgtccccgtgggccgagcgcacttttttcttgtccgggtgcgctcagtcactggtgcctgagaggaaacagtggaggcagcggggcaggtcgcctggggcgtcggcgattatattgcggccgagccggggcgcgccgggaaaggccgggagggcggcggcgcgcgggggctgggcgaggccccgcgacccgcgagggaggcggcgcgaagccgaggcggcgggcgcaagagccgggcatgagcgcccagtagctgagcgcccgcggctgcctggcctcagaagcgacgcgcgagcgcgggcgggcggcagcagcgacgtagcccggcggtcccggcggcgagagcagccgccccacaggcccccgcggcagtgcggccgagtcgaggctcgctctctggctgcttagcgccgcccgcccgcccggggccgccgccgctgacgccccaatgagttcgtacttcgtgaacccgctgtactccaagtacaaggcggcggctgcggcggcggcggcggcgggcgaggccatcaatcccacttactacgactgtcacttcgcgcccgaggtcggcggccgtcacgccgccgccgcagcagccctgcagctctatggcaacagcgccgccggcttcccgcacgcgcccccgcaggcgcacgcgcacccgcacccgtccccgccgccctccgggactgggtgcggcggtagggaaggccggggccaggagtacttccaccccggcgggggcagcccggccgctgcctaccaggccgccccccctcctcctccgcatcctccgcctccgccgccacctcccccctgcggcgggattgcctgtcacggggagcccgcgaagttttacggatacgataacttacagagacagccgatttttacgacccagcaagaggccgagctggtacaatatcctgactgtaaatcgtccagtggtaatattggcgaggacccagaccacttaaatcagagctcgtctccttctcaaatgtttccgtggatgagaccacaagctcctggtagacgaagaggaagacaaacctacagtcgcttccaaactctagagttggaaaaggaatttctttttaacccctatctgaccaggaaaagaagaatcgaggtttcccacgccctagccctcaccgagagacaggtaaaaatctggttccagaacaggagaatgaaatggaaaaaggaaaacaacaaggacaaatttcccgtttcccggcaggaggtgaaggacggggaaacgaaaaaggaagcccaagagctggaggaagacagagccgaaggcctgacaaattaacttctacctttaaaatttaccacagactattaaaactaataatcaccatatgctgtggacaccacctattttctttgttggaaaggaccttacctgtgtttcaagctaccttcatgtcactgctcttgaggttttctgtgctttgagagggatttgggtgtttaaaaaagtttctagtatcacatagaagctgtccttgagctgtcctatggaagggtaatttgatactgaccttgtagctatatttttataatggtttttaatgtctgagctagtgatttgcctcaacaacgtaaacttcctaatgattagcacttaataattgcatataaaatgctttattaattaaacaagtgcacttgaacattttaatatttgtggtgagtaaattaaaaggagtttattaattaaaaaaaattatgtctgcagaatactttatattatttgattacaatgtattatttatggattttttattctttcctttataatgaatagttcgggtgcgttttgtttactcctaaaaggtttctttgcgtattttctaaatgtaatatctcggggaaaatattagaaaagcacgtattagctgaagaatgtaacttgtagtccagctctgcagcttccttaaacttaagaaaaagattgggccagtgacaagaatttaaagacaatgtccaagttgacaattatttttctatagtccatacaaattaaataatctggcaactctggcaaatcgccttgtaaaatgcgtctcattttttaacttgctttcgttttgaaccgcccttgtaatcgcctgaaatcgctagttctttatgcggtggctgccgctgtgttccgttattttcagtaggtgtcatatttatttgtattgcctttgttctgttcgccgctggttttaaaccagcttgctgtgtgcatctcagacgtcggttggtacgtcctccgctgttcttcaggaaagcgatagcctcacctatttgaaacaagccctgagaggaaacgcagaaaaacctgagtgtaaacaactccggaatgtcgctagctccttagtaaataaatgaatctctttctggaaaaaaaaaaaaaaaaa

//

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:3234 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: NAS
            GeneID:3234 -> Molecular function: GO:0043565 [sequence-specific DNA binding] evidence: IEA
            GeneID:3234 -> Biological process: GO:0000122 [negative regulation of transcription from RNA polymerase II promoter] evidence: IEA
            GeneID:3234 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IEA
            GeneID:3234 -> Biological process: GO:0006355 [regulation of transcription, DNA-dependent] evidence: NAS
            GeneID:3234 -> Biological process: GO:0008595 [anterior/posterior axis specification, embryo] evidence: NAS
            GeneID:3234 -> Biological process: GO:0048705 [skeletal system morphogenesis] evidence: IEA
            GeneID:3234 -> Cellular component: GO:0005634 [nucleus] evidence: NAS