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2024-04-19 15:02:13, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_000523 2341 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens homeobox D13 (HOXD13), mRNA.
ACCESSION NM_000523
VERSION NM_000523.3 GI:116734701
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 2341)
AUTHORS Puthiyaveetil,A.G., Heid,B., Reilly,C.M., HogenEsch,H. and
Caudell,D.L.
TITLE A NUP98-HOXD13 leukemic fusion gene leads to impaired class switch
recombination and antibody production
JOURNAL Exp. Hematol. 40 (8), 622-633 (2012)
PUBMED 22613470
REMARK GeneRIF: findings show that expression of NUP98-HOXD13 impairs
class switch recombination and reduces the antibody-mediated immune
response, in addition to its role in leukemia
REFERENCE 2 (bases 1 to 2341)
AUTHORS Wang,B., Xu,B., Cheng,Z., Zhou,X., Wang,J., Yang,G., Cheng,L.,
Yang,J. and Ma,X.
TITLE A novel non-synonymous mutation in the homeodomain of HOXD13 causes
synpolydactyly in a Chinese family
JOURNAL Clin. Chim. Acta 413 (13-14), 1049-1052 (2012)
PUBMED 22374128
REMARK GeneRIF: This finding expands the phenotypic spectrum associated
with HOXD13 mutations and advances our understanding of human limb
development.
REFERENCE 3 (bases 1 to 2341)
AUTHORS Brison,N., Debeer,P., Fantini,S., Oley,C., Zappavigna,V.,
Luyten,F.P. and Tylzanowski,P.
TITLE An N-terminal G11A mutation in HOXD13 causes synpolydactyly and
interferes with Gli3R function during limb pre-patterning
JOURNAL Hum. Mol. Genet. 21 (11), 2464-2475 (2012)
PUBMED 22373878
REMARK GeneRIF: Misexpression of HOXD13(G11A) in the developing chick limb
phenocopied the human SPD phenotype
REFERENCE 4 (bases 1 to 2341)
AUTHORS Xin,Q., Li,L., Li,J., Qiu,R., Guo,C., Gong,Y. and Liu,Q.
TITLE Eight-alanine duplication in homeobox D13 in a Chinese family with
synpolydactyly
JOURNAL Gene 499 (1), 48-51 (2012)
PUBMED 22406499
REMARK GeneRIF: Correlation between Synpolydactyly and alanine expansion
in HOXD13.
REFERENCE 5 (bases 1 to 2341)
AUTHORS Jin,H., Lin,P.F., Wang,Q.M., Mao,F., Cai,Y. and Gong,Y.Q.
TITLE [Synpolydactyly in a Chinese kindred: mutation detection, prenatal
ultrasonographic and molecular diagnosis]
JOURNAL Zhonghua Yi Xue Yi Chuan Xue Za Zhi 28 (6), 601-605 (2011)
PUBMED 22161087
REMARK GeneRIF: HOXD13 gene mutation was responsible for the
synpolydactyly (SPD) phenotype in this family.
REFERENCE 6 (bases 1 to 2341)
AUTHORS Goodman,F., Giovannucci-Uzielli,M.L., Hall,C., Reardon,W.,
Winter,R. and Scambler,P.
TITLE Deletions in HOXD13 segregate with an identical, novel foot
malformation in two unrelated families
JOURNAL Am. J. Hum. Genet. 63 (4), 992-1000 (1998)
PUBMED 9758628
REFERENCE 7 (bases 1 to 2341)
AUTHORS Johnson,R.L. and Tabin,C.J.
TITLE Molecular models for vertebrate limb development
JOURNAL Cell 90 (6), 979-990 (1997)
PUBMED 9323126
REMARK Review article
REFERENCE 8 (bases 1 to 2341)
AUTHORS Akarsu,A.N., Stoilov,I., Yilmaz,E., Sayli,B.S. and Sarfarazi,M.
TITLE Genomic structure of HOXD13 gene: a nine polyalanine duplication
causes synpolydactyly in two unrelated families
JOURNAL Hum. Mol. Genet. 5 (7), 945-952 (1996)
PUBMED 8817328
REMARK GeneRIF: Gene Structure and Report of Nine Polyalanine Duplications
in Families with Synpolydactyly, Type II
REFERENCE 9 (bases 1 to 2341)
AUTHORS D'Esposito,M., Morelli,F., Acampora,D., Migliaccio,E., Simeone,A.
and Boncinelli,E.
TITLE EVX2, a human homeobox gene homologous to the even-skipped
segmentation gene, is localized at the 5' end of HOX4 locus on
chromosome 2
JOURNAL Genomics 10 (1), 43-50 (1991)
PUBMED 1675198
REFERENCE 10 (bases 1 to 2341)
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 AC009336.13 and BX100910.1.
This sequence is a reference standard in the RefSeqGene project.
On Oct 26, 2006 this sequence version replaced gi:23510371.
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. Mutations in this particular gene cause
synpolydactyly. [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 :: AI971733.1, AI858239.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025090, ERS025092 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-868 AC009336.13 76793-77660
869-2204 AC009336.13 78469-79804
2205-2341 BX100910.1 1-137 c
FEATURES Location/Qualifiers
source 1..2341
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="2"
/map="2q31.1"
gene 1..2341
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/note="homeobox D13"
/db_xref="GeneID:3239"
/db_xref="HGNC:5136"
/db_xref="MIM:142989"
exon 1..868
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/inference="alignment:Splign:1.39.8"
STS 3..1297
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/db_xref="UniSTS:483796"
STS 5..509
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/standard_name="PMC23843P1"
/db_xref="UniSTS:272211"
variation 49
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="c"
/replace="g"
/db_xref="dbSNP:144577020"
STS 62..1169
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/db_xref="UniSTS:481600"
CDS 88..1119
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/note="homeo box D13; homeo box 4I; homeobox protein
Hox-4I"
/codon_start=1
/product="homeobox protein Hox-D13"
/protein_id="NP_000514.2"
/db_xref="GI:116734702"
/db_xref="CCDS:CCDS2264.2"
/db_xref="GeneID:3239"
/db_xref="HGNC:5136"
/db_xref="MIM:142989"
/translation="
MSRAGSWDMDGLRADGGGAGGAPASSSSSSVAAAAASGQCRGFLSAPVFAGTHSGRAAAAAAAAAAAAAAASGFAYPGTSERTGSSSSSSSSAVVAARPEAPPAKECPAPTPAAAAAAPPSAPALGYGYHFGNGYYSCRMSHGVGLQQNALKSSPHASLGGFPVEKYMDVSGLASSSVPANEVPARAKEVSFYQGYTSPYQHVPGYIDMVSTFGSGEPRHEAYISMEGYQSWTLANGWNSQVYCTKDQPQGSHFWKSSFPGDVALNQPDMCVYRRGRKKRVPYTKLQLKELENEYAINKFINKDKRRRISAATNLSERQVTIWFQNRRVKDKKIVSKLKDTVS
"
misc_feature <469..627
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/note="Hox protein A13 N terminal; Region: HoxA13_N;
pfam12284"
/db_xref="CDD:152719"
misc_feature 916..1086
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/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(916..930,934..936,985..987,1003..1005,1042..1044,
1048..1053,1060..1065,1069..1077,1081..1086)
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/note="DNA binding site [nucleotide binding]"
/db_xref="CDD:28970"
misc_feature order(922..924,931..933,1051..1053,1060..1065,1072..1074)
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/note="specific DNA base contacts [nucleotide binding];
other site"
/db_xref="CDD:28970"
variation 256..267
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="(gcg(15_22))"
/db_xref="dbSNP:193922939"
variation 258..269
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace=""
/replace="ggcggcggcggc"
/db_xref="dbSNP:3832095"
variation 291
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="g"
/db_xref="dbSNP:2518053"
variation 335
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="c"
/replace="t"
/db_xref="dbSNP:369711414"
variation 347
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="c"
/replace="g"
/db_xref="dbSNP:139995491"
variation 383
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="c"
/replace="t"
/db_xref="dbSNP:143487752"
variation 384
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="g"
/replace="t"
/db_xref="dbSNP:373546423"
variation 391
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="c"
/db_xref="dbSNP:201821228"
variation 401
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="c"
/db_xref="dbSNP:200514497"
variation 428
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="c"
/db_xref="dbSNP:369717765"
variation 441
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="g"
/replace="t"
/db_xref="dbSNP:372534114"
variation 480
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="g"
/db_xref="dbSNP:847195"
variation 492
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="c"
/db_xref="dbSNP:201600075"
variation 513
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="c"
/replace="t"
/db_xref="dbSNP:140031618"
variation 556
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="g"
/db_xref="dbSNP:187698441"
variation 561
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:371806521"
variation 587
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="g"
/db_xref="dbSNP:200067774"
variation 620
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="c"
/replace="t"
/db_xref="dbSNP:201904809"
variation 628
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="g"
/db_xref="dbSNP:148979353"
variation 630
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="c"
/db_xref="dbSNP:13392701"
variation 676
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="t"
/db_xref="dbSNP:374086950"
variation 704
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="g"
/db_xref="dbSNP:147720746"
variation 716
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="c"
/replace="t"
/db_xref="dbSNP:200274374"
variation 761
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="c"
/replace="g"
/db_xref="dbSNP:367674921"
variation 770
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="g"
/replace="t"
/db_xref="dbSNP:121912541"
variation 777
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="c"
/replace="g"
/db_xref="dbSNP:142600246"
variation 841
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="c"
/db_xref="dbSNP:35290213"
variation 844
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="c"
/replace="t"
/db_xref="dbSNP:374920154"
exon 869..2327
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/inference="alignment:Splign:1.39.8"
variation 877
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="g"
/replace="t"
/db_xref="dbSNP:373737493"
STS 880..1113
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/standard_name="Hoxd13"
/db_xref="UniSTS:265598"
variation 897
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="g"
/db_xref="dbSNP:185454060"
variation 900
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="c"
/replace="t"
/db_xref="dbSNP:199982017"
variation 901
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="g"
/replace="t"
/db_xref="dbSNP:138630870"
variation 907
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="c"
/replace="t"
/db_xref="dbSNP:200750564"
variation 939
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="c"
/replace="g"
/db_xref="dbSNP:149097061"
STS 953..1569
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/standard_name="HOXD13_3043"
/db_xref="UniSTS:462256"
variation 976
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="g"
/db_xref="dbSNP:372343718"
variation 998
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="g"
/db_xref="dbSNP:376366804"
variation 1003
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="c"
/replace="t"
/db_xref="dbSNP:28933082"
variation 1026
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="g"
/db_xref="dbSNP:150319624"
variation 1034
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="c"
/replace="g"
/db_xref="dbSNP:28928892"
variation 1051
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="c"
/db_xref="dbSNP:28928891"
variation 1061
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="g"
/db_xref="dbSNP:104893635"
variation 1092
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="c"
/replace="t"
/db_xref="dbSNP:369216922"
variation 1138
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="c"
/replace="t"
/db_xref="dbSNP:111593893"
variation 1168
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:199549554"
variation 1285
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="c"
/replace="t"
/db_xref="dbSNP:188371903"
variation 1292
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="g"
/db_xref="dbSNP:138557314"
variation 1355
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="t"
/db_xref="dbSNP:141649575"
variation 1359
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="g"
/db_xref="dbSNP:114386082"
variation 1430
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="c"
/replace="t"
/db_xref="dbSNP:72923426"
variation 1471..1472
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace=""
/replace="t"
/db_xref="dbSNP:146564993"
variation 1479
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="t"
/db_xref="dbSNP:72923428"
variation 1516
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="g"
/db_xref="dbSNP:146173864"
variation 1627
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="g"
/db_xref="dbSNP:370850321"
variation 1822
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="g"
/db_xref="dbSNP:137896965"
variation 1856
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="g"
/db_xref="dbSNP:73029937"
variation 1883
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="g"
/replace="t"
/db_xref="dbSNP:12615946"
variation 1921
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="g"
/db_xref="dbSNP:112259280"
variation 1942
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="c"
/replace="t"
/db_xref="dbSNP:150914949"
variation 2108
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="g"
/replace="t"
/db_xref="dbSNP:184749616"
variation 2162
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="a"
/replace="g"
/db_xref="dbSNP:28661358"
variation 2181
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
/replace="c"
/replace="t"
/db_xref="dbSNP:189204555"
polyA_signal 2305..2310
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
polyA_site 2327
/gene="HOXD13"
/gene_synonym="BDE; BDSD; HOX4I; SPD"
ORIGIN
gagaaaggagaggagggaggaggcgcgccgcgccatggtgtcctgcgcggggccagggccagggccggggccgggccaggccgggccatgagccgcgccgggagctgggacatggacgggctgcgggcagacggcgggggcgccggtggcgccccggcctcttcctcctcctcatcggtggcggcggcggcggcgtcaggccagtgccgcggctttctctccgcgcctgtgttcgccgggacgcattcggggcgggcggcggcggcggcagcggcggctgcggcggcggcggcggcagcctccggctttgcgtaccccgggacctctgagcgcacgggctcttcctcgtcgtcgtcctcttctgccgttgtagcggcgcgcccggaggctcccccagccaaagagtgcccagcacccacgcctgcagcggccgctgcagcgcccccgagcgctccagcgctgggctacggctaccacttcggcaacggctactacagctgccgtatgtcgcacggcgtgggcttacagcagaatgcgctcaagtcatcgccgcacgcctcgctgggaggctttcccgtggagaagtacatggacgtgtcaggcctggcgagcagcagcgtaccggccaacgaggtgccagcgcgagccaaggaggtatccttctaccagggctatacgagcccttaccagcacgtgcccggctatatcgacatggtgtccactttcggctccggggagcctcggcacgaggcctacatctccatggaggggtaccagtcctggacgctggctaacgggtggaacagccaggtgtactgcaccaaggaccagccacaggggtcccacttttggaaatcttcctttccaggggatgtggctctaaatcagccggacatgtgcgtctaccgaagagggaggaagaagagagtgccttacaccaaactgcagcttaaagaactggagaacgagtatgccattaacaaattcattaacaaggacaagcggcggcgtatctcggctgctacgaacctatctgagagacaagtgaccatttggtttcagaaccgaagagtgaaggacaagaaaattgtctccaagctcaaagatactgtctcctgatgtggtccaggttggccacagacagcttagaagccattcggttgtctccaaaaggcctttggaaagacttgaatatgtatttaattccccccaccccctgccaatggtggcaaattttgtgaattgtttttctctcttccccttatctggctctaaaaccttctgctgcccaacctgactttgtagttctgatttttacttgtttattattggttttgttcttgcctagggtttttaaaatatctgtttttaatgttttgtttctccctccaggccagtataaagggacttgaagtattttttaataatccgccccccaatgaacttcagaagtgccattctgatttaagggtttttttaaaaaattactttatttgttcattcccagcactgattatcttcataatccattaggacagaatggttttcagtcgttcatatcctgtaattaggtaattgaatcattagctctcagcagttgccctgaggcaagtggaaaggcaggcagtgctctggggtcaccgagaaagtctaaaaacaggaggctgaaggtactgtgatggctttaaaaatggccaccttattaaatagggattgtatcaatattgaaatgaagacaatctttccaactttgggtgtttcacttgctgttttaattgtttgtttttaacactttgtaggtttgtgttttcataatctttaatttgaaactcatgtgtcctcatggatcgtggatgccttcatttcttgagctctcaatgcagacatttaaatggctgcaatcagtagagtgacccgcggatggcataaatgcacctccttttcttggccttggatctatgggtctgggattgtggtcatctcctcaatcctcaaaaagaggctgaatcaatgtggccgtgggtgggaacttacatacagaacccaatgaagaacttgactgtctaaacaagggggcctcgcatggagctgtaaagcatctaacaaatatgaaaaatgtgaagttccaaggtccaagaagaaaaataatgatgtttctgaaagtgatgataaataattacttttaaagtgctgcatatttatacaattgagagattatttttgtaaatgcaatgtctgtgagctgggatacatgggcagtgcttcagacatttaaaaatcactttttactcctagggagatgccaataaacagaactcttttgtttcaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:3239 -> Molecular function: GO:0003677 [DNA binding] evidence: TAS
GeneID:3239 -> Molecular function: GO:0003682 [chromatin binding] evidence: IEA
GeneID:3239 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: IEA
GeneID:3239 -> Molecular function: GO:0043565 [sequence-specific DNA binding] evidence: IEA
GeneID:3239 -> Biological process: GO:0001501 [skeletal system development] evidence: IEA
GeneID:3239 -> Biological process: GO:0006355 [regulation of transcription, DNA-dependent] evidence: TAS
GeneID:3239 -> Biological process: GO:0006366 [transcription from RNA polymerase II promoter] evidence: TAS
GeneID:3239 -> Biological process: GO:0007275 [multicellular organismal development] evidence: TAS
GeneID:3239 -> Biological process: GO:0009952 [anterior/posterior pattern specification] evidence: IEA
GeneID:3239 -> Biological process: GO:0030539 [male genitalia development] evidence: IEA
GeneID:3239 -> Biological process: GO:0042127 [regulation of cell proliferation] evidence: IEA
GeneID:3239 -> Biological process: GO:0042733 [embryonic digit morphogenesis] evidence: IEA
GeneID:3239 -> Biological process: GO:0045944 [positive regulation of transcription from RNA polymerase II promoter] evidence: IEA
GeneID:3239 -> Biological process: GO:0048619 [embryonic hindgut morphogenesis] evidence: IEA
GeneID:3239 -> Biological process: GO:0060527 [prostate epithelial cord arborization involved in prostate glandular acinus morphogenesis] evidence: IEA
GeneID:3239 -> Biological process: GO:0060571 [morphogenesis of an epithelial fold] evidence: IEA
GeneID:3239 -> Biological process: GO:0060602 [branch elongation of an epithelium] evidence: IEA
GeneID:3239 -> Biological process: GO:0060687 [regulation of branching involved in prostate gland morphogenesis] evidence: IEA
GeneID:3239 -> Cellular component: GO:0005634 [nucleus] evidence: IEA
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