LOCUS       NM_138281               2012 bp    mRNA    linear   PRI 13-APR-2013
DEFINITION  Homo sapiens distal-less homeobox 4 (DLX4), transcript variant 1,
            mRNA.
ACCESSION   NM_138281
VERSION     NM_138281.2  GI:221316719
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 2012)
  AUTHORS   Zhang,L., Yang,M., Gan,L., He,T., Xiao,X., Stewart,M.D., Liu,X.,
            Yang,L., Zhang,T., Zhao,Y. and Fu,J.
  TITLE     DLX4 upregulates TWIST and enhances tumor migration, invasion and
            metastasis
  JOURNAL   Int. J. Biol. Sci. 8 (8), 1178-1187 (2012)
   PUBMED   23091415
  REMARK    GeneRIF: DLX4 induces cancer cells to undergo epithelial to
            mesenchymal transition through TWIST, enhancing tumor migration,
            invasion and metastasis.
REFERENCE   2  (bases 1 to 2012)
  AUTHORS   Sun,Y.Y., Lu,M., Xi,X.W., Qiao,Q.Q., Chen,L.L., Xu,X.M. and
            Feng,Y.J.
  TITLE     Regulation of epithelial-mesenchymal transition by homeobox gene
            DLX4 in JEG-3 trophoblast cells: a role in preeclampsia
  JOURNAL   Reprod Sci 18 (11), 1138-1145 (2011)
   PUBMED   21602546
  REMARK    GeneRIF: findings suggest that decreased expression of homeobox
            protein DLX-4 leads to the pathogenesis of preeclampsia by
            inhibiting epithelial-mesenchymal transition in trophoblasts
REFERENCE   3  (bases 1 to 2012)
  AUTHORS   Trinh,B.Q., Barengo,N. and Naora,H.
  TITLE     Homeodomain protein DLX4 counteracts key transcriptional control
            mechanisms of the TGF-beta cytostatic program and blocks the
            antiproliferative effect of TGF-beta
  JOURNAL   Oncogene 30 (24), 2718-2729 (2011)
   PUBMED   21297662
  REMARK    GeneRIF: The ability of DLX4 to counteract key transcriptional
            control mechanisms of the TGF-beta cytostatic program could
            explain, in part, the resistance of tumors to the antiproliferative
            effect of TGF-beta.
REFERENCE   4  (bases 1 to 2012)
  AUTHORS   Jugessur,A., Shi,M., Gjessing,H.K., Lie,R.T., Wilcox,A.J.,
            Weinberg,C.R., Christensen,K., Boyles,A.L., Daack-Hirsch,S.,
            Nguyen,T.T., Christiansen,L., Lidral,A.C. and Murray,J.C.
  TITLE     Maternal genes and facial clefts in offspring: a comprehensive
            search for genetic associations in two population-based cleft
            studies from Scandinavia
  JOURNAL   PLoS ONE 5 (7), E11493 (2010)
   PUBMED   20634891
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
            Publication Status: Online-Only
REFERENCE   5  (bases 1 to 2012)
  AUTHORS   Man,Y.G., Schwartz,A., Levine,P.H., Teal,C. and Berg,P.E.
  TITLE     BP1, a putative signature marker for inflammatory breast cancer and
            tumor aggressiveness
  JOURNAL   Cancer Biomark 5 (1), 9-17 (2009)
   PUBMED   19242057
  REMARK    GeneRIF: High BP1 expression is associated with inflammatory breast
            cancer and tumor aggressiveness
REFERENCE   6  (bases 1 to 2012)
  AUTHORS   Price,J.A., Bowden,D.W., Wright,J.T., Pettenati,M.J. and Hart,T.C.
  TITLE     Identification of a mutation in DLX3 associated with
            tricho-dento-osseous (TDO) syndrome
  JOURNAL   Hum. Mol. Genet. 7 (3), 563-569 (1998)
   PUBMED   9467018
REFERENCE   7  (bases 1 to 2012)
  AUTHORS   Quinn,L.M., Latham,S.E. and Kalionis,B.
  TITLE     A distal-less class homeobox gene, DLX4, is a candidate for
            regulating epithelial-mesenchymal cell interactions in the human
            placenta
  JOURNAL   Placenta 19 (1), 87-93 (1998)
   PUBMED   9481790
REFERENCE   8  (bases 1 to 2012)
  AUTHORS   Morasso,M.I., Yonescu,R., Griffin,C.A. and Sargent,T.D.
  TITLE     Localization of human DLX8 to chromosome 17q21.3-q22 by
            fluorescence in situ hybridization
  JOURNAL   Mamm. Genome 8 (4), 302-303 (1997)
   PUBMED   9096128
REFERENCE   9  (bases 1 to 2012)
  AUTHORS   Quinn,L.M., Johnson,B.V., Nicholl,J., Sutherland,G.R. and
            Kalionis,B.
  TITLE     Isolation and identification of homeobox genes from the human
            placenta including a novel member of the Distal-less family, DLX4
  JOURNAL   Gene 187 (1), 55-61 (1997)
   PUBMED   9073066
REFERENCE   10 (bases 1 to 2012)
  AUTHORS   Nakamura,S., Stock,D.W., Wydner,K.L., Bollekens,J.A., Takeshita,K.,
            Nagai,B.M., Chiba,S., Kitamura,T., Freeland,T.M., Zhao,Z.,
            Minowada,J., Lawrence,J.B., Weiss,K.M. and Ruddle,F.H.
  TITLE     Genomic analysis of a new mammalian distal-less gene: Dlx7
  JOURNAL   Genomics 38 (3), 314-324 (1996)
   PUBMED   8975708
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from BC016145.1, DR004878.1,
            BX113580.1 and CB131875.1.
            This sequence is a reference standard in the RefSeqGene project.
            On Jan 24, 2009 this sequence version replaced gi:20143961.
            
            Summary: Many vertebrate homeo box-containing genes have been
            identified on the basis of their sequence similarity with
            Drosophila developmental genes. Members of the Dlx gene family
            contain a homeobox that is related to that of Distal-less (Dll), a
            gene expressed in the head and limbs of the developing fruit fly.
            The Distal-less (Dlx) family of genes comprises at least 6
            different members, DLX1-DLX6. The DLX proteins are postulated to
            play a role in forebrain and craniofacial development. Three
            transcript variants have been described for this gene, however, the
            full length nature of one variant has not been described. Studies
            of the two splice variants revealed that one encoded isoform
            functions as a repressor of the beta-globin gene while the other
            isoform lacks that function. [provided by RefSeq, Jul 2008].
            
            Transcript Variant: This variant (1) encodes the longer isoform (a,
            also known as BP1), which functions as a repressor of the
            beta-globin gene.
            
            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 :: BC016145.1, AF254115.1 [ECO:0000332]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-71                BC016145.1         1-71
            72-213              BC016145.1         73-214
            214-554             DR004878.1         92-432
            555-1350            BC016145.1         556-1351
            1351-1916           BX113580.1         134-699
            1917-2012           CB131875.1         1-96                c
FEATURES             Location/Qualifiers
     source          1..2012
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="17"
                     /map="17q21.33"
     gene            1..2012
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /note="distal-less homeobox 4"
                     /db_xref="GeneID:1748"
                     /db_xref="HGNC:2917"
                     /db_xref="HPRD:03553"
                     /db_xref="MIM:601911"
     exon            1..554
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /inference="alignment:Splign:1.39.8"
     misc_feature    44..46
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /note="upstream in-frame stop codon"
     variation       65..66
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:71146955"
     variation       87
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372907782"
     variation       214
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:58769681"
     variation       244
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202019671"
     variation       248
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371161696"
     variation       261
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367638945"
     CDS             272..994
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /note="isoform a is encoded by transcript variant 1;
                     distal-less homeo box 9; beta protein 1; homeobox protein
                     DLX-4; distal-less homeo box 7; homeobox protein DLX-7;
                     homeobox protein DLX-8"
                     /codon_start=1
                     /product="homeobox protein DLX-4 isoform a"
                     /protein_id="NP_612138.1"
                     /db_xref="GI:20143962"
                     /db_xref="CCDS:CCDS11555.1"
                     /db_xref="GeneID:1748"
                     /db_xref="HGNC:2917"
                     /db_xref="HPRD:03553"
                     /db_xref="MIM:601911"
                     /translation="

MTSLPCPLPGRDASKAVFPDLAPVPSVAAAYPLGLSPTTAASPNLSYSRPYGHLLSYPYTEPANPGDSYLSCQQPAALSQPLCGPAEHPQELEADSEKPRLSPEPSERRPQAPAKKLRKPRTIYSSLQLQHLNQRFQHTQYLALPERAQLAAQLGLTQTQVKIWFQNKRSKYKKLLKQNSGGQEGDFPGRTFSVSPCSPPLPSLWDLPKAGTLPTSGYGNSFGAWYQHHSSDVLASPQMM

"
     misc_feature    623..793
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /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(623..637,641..643,692..694,710..712,749..751,
                     755..760,767..772,776..784,788..793)
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /note="DNA binding site [nucleotide binding]"
                     /db_xref="CDD:28970"
     misc_feature    order(629..631,638..640,758..760,767..772,779..781)
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /note="specific DNA base contacts [nucleotide binding];
                     other site"
                     /db_xref="CDD:28970"
     variation       303
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200991862"
     variation       345
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:145781048"
     variation       356
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:148979255"
     variation       366
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199532173"
     variation       380
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:376092706"
     variation       381
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:376997322"
     variation       389
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:370379441"
     variation       394
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372780650"
     variation       399
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:143763914"
     variation       402
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:61749026"
     variation       451
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:377467088"
     variation       466
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370951089"
     variation       475
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200579401"
     variation       502
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:200168432"
     variation       511
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368222487"
     variation       548
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:145736583"
     variation       553
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:138634383"
     exon            555..751
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /inference="alignment:Splign:1.39.8"
     variation       613..614
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:370138317"
     variation       624
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372156240"
     STS             643..939
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /standard_name="PMC20354P1"
                     /db_xref="UniSTS:271934"
     variation       675
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:151318731"
     variation       730
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:370377249"
     variation       733
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:150742579"
     STS             736..789
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /standard_name="ksks321"
                     /db_xref="UniSTS:514366"
     variation       742
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:139118373"
     exon            752..2010
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /inference="alignment:Splign:1.39.8"
     variation       776
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149498057"
     variation       778
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200916126"
     variation       796
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:146002721"
     variation       817
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:368164202"
     variation       827
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:139954414"
     variation       867
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150024578"
     variation       875
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372590740"
     variation       878
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:201875580"
     variation       889
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146281851"
     variation       941
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:1058559"
     variation       978
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202154782"
     variation       979
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369561537"
     variation       1008
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:192533761"
     variation       1009
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371538328"
     variation       1034..1035
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace=""
                     /replace="agcccaggacccaggcagtccacctgcac"
                     /db_xref="dbSNP:60243053"
     variation       1041
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:201620636"
     variation       1134
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1058560"
     variation       1167
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1058561"
     variation       1316
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:75953192"
     variation       1321
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142428478"
     variation       1351
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1058562"
     variation       1421..1422
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:201251660"
     variation       1453
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146419987"
     variation       1459
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1058564"
     STS             1510..1618
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /standard_name="RH36424"
                     /db_xref="UniSTS:9030"
     variation       1556
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184512405"
     variation       1636..1637
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:375951477"
     variation       1636
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:143029210"
     variation       1637..1638
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:11429140"
     variation       1651..1652
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace=""
                     /replace="a"
                     /replace="aaa"
                     /replace="aaaa"
                     /replace="aaaaa"
                     /db_xref="dbSNP:10677419"
     variation       1652..1653
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace=""
                     /replace="aa"
                     /replace="aaaaa"
                     /db_xref="dbSNP:36061264"
     variation       1682..1683
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:34108300"
     variation       1781
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:4793623"
     variation       1804
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147873124"
     STS             1812..1963
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /standard_name="RH12668"
                     /db_xref="UniSTS:49797"
     variation       1819
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:8066341"
     variation       1960
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:373728187"
     polyA_signal    1986..1991
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
     polyA_site      2010
                     /gene="DLX4"
                     /gene_synonym="BP1; DLX7; DLX8; DLX9"
ORIGIN      

ccgggaaccgaacccgatggagaggagggggcccccatggatttagggggggaggggaaagtcatggggggcacccccccggaacccctttcccaggcgcgcgttctccgctgaaagaggctcagagagacactttctccgggatcttaagtgtgggggctgctggctggggggcccgtccggcccaacgccggaggcttggaaaagagagttggcagcgggagcggactacgtgccgggccatggcccttctgcccgggccctggccacaatgacctctttgccctgccccctccccggccgggacgcctccaaagctgtcttcccagacctcgcccctgtcccgtcggtagcggctgcctacccgcttggcttgtcccctacaaccgcagcctcccccaatttgtcctactccaggccgtatggccacctcctgtcttacccctacaccgagccagcgaaccccggagactcctacctgtcctgccagcaacccgcggcgctctctcagcccctctgcggacctgcagagcaccctcaggaactcgaggcagactcggagaagccgcggctgtccccggaaccctccgagcggcgccctcaggcccccgccaaaaagctccgcaagccgaggaccatctactccagcctgcagctgcagcacctaaaccagcgtttccagcacacgcagtacctggcgctgcccgagagggcccagctggcagcgcagctcggcctcacccagacccaggtaaagatctggtttcagaacaaacgctccaagtataagaagctcctgaagcagaattctggggggcaggaaggggacttccctgggaggaccttctctgtgtctccctgctccccacccctcccctccctctgggatctacccaaggcagggaccctgcccaccagtggctatggcaacagctttggagcctggtatcagcatcactcctcagatgtcctggcttcgcctcagatgatgtgaatctggggaagggcgggtcaggcccacagccttcctgcaaagcccaggacccaggcagtccacctgcaccccttctgggctgggaggaaaccagctccagatgggttttctctggaggacaagcagttagaggagaaaaaggaatggagcagagcctgtacccctaaccctaacagctaaatcaaggacctcagccttatataatcattgtccccaccactaccatggactggacaccttcactccagctggacaaagactctggagagagagccattggctggagttgagactgtccccagaacccttggtcttgccactcccccactccttcttccctctctccctttctcctctccctgctttcttgaaaaggactgaatcgccactacagcctgggtgcaaaatcagcaagaaacattgagtatttttttttctttgtatgcctttggccttgcacaacccatttgtgagcaaaagcagaagtggaccaccatcagctcccacccacccagcgatttttccttggaggtcagcccgttacccccataactgatttacctacttaccatactgggaggtagaagagatgcagagaaatgtggaatttgtggacctatgggtaatttatgctttcctcctaaaaaaaaaaaaaaagccctctttcccaccccctccccatctcccctttttgaatagataatggatccaattatccatataattcaataggtatttattgagaggctcccttctattccccatccctaatccctaacgaacccacgggcacacacttttggaaacctggtaaagtaacacttagggggaaatggggacaaactggctctctggattagtgcgggtatagacacccccaaataggtgggtaggcccattgattcagctccttgcagctgtctctgttcaaaggaactgtgcagatttagaacgaattggagcttgagcttcacaccaccagcttccagagattaaagtttgtacaaaacattgcaaa

//

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:1748 -> Molecular function: GO:0000976 [transcription regulatory region sequence-specific DNA binding] evidence: IEA
            GeneID:1748 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: NAS
            GeneID:1748 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
            GeneID:1748 -> Molecular function: GO:0043565 [sequence-specific DNA binding] evidence: IDA
            GeneID:1748 -> Biological process: GO:0006355 [regulation of transcription, DNA-dependent] evidence: NAS
            GeneID:1748 -> Biological process: GO:0007275 [multicellular organismal development] evidence: IEA
            GeneID:1748 -> Cellular component: GO:0005634 [nucleus] evidence: NAS