LOCUS       NM_001256114            1784 bp    mRNA    linear   PRI 07-JUL-2013
DEFINITION  Homo sapiens LIM homeobox 8 (LHX8), transcript variant 2, mRNA.
ACCESSION   NM_001256114
VERSION     NM_001256114.1  GI:368711325
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 1784)
  AUTHORS   Jagarlamudi,K. and Rajkovic,A.
  TITLE     Oogenesis: transcriptional regulators and mouse models
  JOURNAL   Mol. Cell. Endocrinol. 356 (1-2), 31-39 (2012)
   PUBMED   21856374
  REMARK    Review article
REFERENCE   2  (bases 1 to 1784)
  AUTHORS   Paschou P, Stylianopoulou E, Karagiannidis I, Rizzo R, Tarnok Z,
            Wolanczyk T, Hebebrand J, Nothen MM, Lehmkuhl G, Farkas L, Nagy P,
            Szymanska U, Lykidis D, Androutsos C, Tsironi V, Koumoula A, Barta
            C, Klidonas S, Ypsilantis P, Simopoulos C, Skavdis G and Grigoriou
            M.
  CONSRTM   TSGeneSEE Consortium
  TITLE     Evaluation of the LIM homeobox genes LHX6 and LHX8 as candidates
            for Tourette syndrome
  JOURNAL   Genes Brain Behav. 11 (4), 444-451 (2012)
   PUBMED   22435649
  REMARK    GeneRIF: Our tagging-single nucleotide polymorphism (tSNP)-based
            association analysis was negative for Tourette syndrome association
            with LHX8.
REFERENCE   3  (bases 1 to 1784)
  AUTHORS   Nat,R., Salti,A., Suciu,L., Strom,S. and Dechant,G.
  TITLE     Pharmacological modulation of the Hedgehog pathway differentially
            affects dorsal/ventral patterning in mouse and human embryonic stem
            cell models of telencephalic development
  JOURNAL   Stem Cells Dev. 21 (7), 1016-1046 (2012)
   PUBMED   22204396
REFERENCE   4  (bases 1 to 1784)
  AUTHORS   Nikopensius,T., Kempa,I., Ambrozaityte,L., Jagomagi,T., Saag,M.,
            Matuleviciene,A., Utkus,A., Krjutskov,K., Tammekivi,V., Piekuse,L.,
            Akota,I., Barkane,B., Krumina,A., Klovins,J., Lace,B., Kucinskas,V.
            and Metspalu,A.
  TITLE     Variation in FGF1, FOXE1, and TIMP2 genes is associated with
            nonsyndromic cleft lip with or without cleft palate
  JOURNAL   Birth Defects Res. Part A Clin. Mol. Teratol. 91 (4), 218-225
            (2011)
   PUBMED   21462296
REFERENCE   5  (bases 1 to 1784)
  AUTHORS   Kim,J.Y., Jeon,S.H., Park,J.Y., Suh,J.D. and Choung,P.H.
  TITLE     Comparative study of LHX8 expression between odontoma and dental
            tissue-derived stem cells
  JOURNAL   J. Oral Pathol. Med. 40 (3), 250-256 (2011)
   PUBMED   21143530
  REMARK    GeneRIF: LHX8 might play an important role in odontoma formation.
            This is 1st report on comparison of LHX8 expression between human
            odontoma-derived mesenchymal cells and normal adult dental
            mesenchymal stem cells and its overexpression in human samples.
REFERENCE   6  (bases 1 to 1784)
  AUTHORS   Qin,Y., Zhao,H., Kovanci,E., Simpson,J.L., Chen,Z.J. and
            Rajkovic,A.
  TITLE     Analysis of LHX8 mutation in premature ovarian failure
  JOURNAL   Fertil. Steril. 89 (4), 1012-1014 (2008)
   PUBMED   17624344
  REMARK    GeneRIF: Mutations in the LHX8 exons are uncommon in Caucasian
            women with premature ovarian failure.
            GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   7  (bases 1 to 1784)
  AUTHORS   Suzumori,N., Pangas,S.A. and Rajkovic,A.
  TITLE     Candidate genes for premature ovarian failure
  JOURNAL   Curr. Med. Chem. 14 (3), 353-357 (2007)
   PUBMED   17305537
  REMARK    Review article
REFERENCE   8  (bases 1 to 1784)
  AUTHORS   Pangas,S.A., Choi,Y., Ballow,D.J., Zhao,Y., Westphal,H.,
            Matzuk,M.M. and Rajkovic,A.
  TITLE     Oogenesis requires germ cell-specific transcriptional regulators
            Sohlh1 and Lhx8
  JOURNAL   Proc. Natl. Acad. Sci. U.S.A. 103 (21), 8090-8095 (2006)
   PUBMED   16690745
  REMARK    GeneRIF: Sohlh1 and Lhx8 are two germ cell-specific, critical
            regulators of oogenesis
REFERENCE   9  (bases 1 to 1784)
  AUTHORS   Vieira,A.R., Avila,J.R., Daack-Hirsch,S., Dragan,E., Felix,T.M.,
            Rahimov,F., Harrington,J., Schultz,R.R., Watanabe,Y., Johnson,M.,
            Fang,J., O'Brien,S.E., Orioli,I.M., Castilla,E.E.,
            Fitzpatrick,D.R., Jiang,R., Marazita,M.L. and Murray,J.C.
  TITLE     Medical sequencing of candidate genes for nonsyndromic cleft lip
            and palate
  JOURNAL   PLoS Genet. 1 (6), E64 (2005)
   PUBMED   16327884
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   10 (bases 1 to 1784)
  AUTHORS   Zhao,Y., Guo,Y.J., Tomac,A.C., Taylor,N.R., Grinberg,A., Lee,E.J.,
            Huang,S. and Westphal,H.
  TITLE     Isolated cleft palate in mice with a targeted mutation of the LIM
            homeobox gene lhx8
  JOURNAL   Proc. Natl. Acad. Sci. U.S.A. 96 (26), 15002-15006 (1999)
   PUBMED   10611327
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from BC036423.1, AC099786.2 and
            BC040321.1.
            
            Summary: The protein encoded by this gene is a member of the LIM
            homeobox family of proteins, which are involved in patterning and
            differentiation of various tissue types. These proteins contain two
            tandemly repeated cysteine-rich double-zinc finger motifs known as
            LIM domains, in addition to a DNA-binding homeodomain. This family
            member is a transcription factor that plays a role in tooth
            morphogenesis. It is also involved in oogenesis and in neuronal
            differentiation. This gene is a candidate gene for cleft palate,
            and it is also associated with odontoma formation. Alternative
            splicing of this gene results in multiple transcript variants.
            [provided by RefSeq, Jan 2012].
            
            Transcript Variant: This variant (2) differs in the 5' UTR, lacks a
            portion of the 5' coding region, and uses a downstream
            translational start codon, compared to variant 1. The encoded
            isoform (2) is shorter at the N-terminus, compared to isoform 1.
            
            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 :: BC036423.1 [ECO:0000332]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-161               BC036423.1         7-167
            162-229             AC099786.2         145902-145969
            230-344             BC036423.1         234-348
            345-345             AC099786.2         149808-149808
            346-510             BC036423.1         350-514
            511-511             AC099786.2         151985-151985
            512-1395            BC036423.1         516-1399
            1396-1784           BC040321.1         2005-2393
FEATURES             Location/Qualifiers
     source          1..1784
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="1"
                     /map="1p31.1"
     gene            1..1784
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /note="LIM homeobox 8"
                     /db_xref="GeneID:431707"
                     /db_xref="HGNC:28838"
                     /db_xref="MIM:604425"
     exon            1..73
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /inference="alignment:Splign:1.39.8"
     exon            74..160
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /inference="alignment:Splign:1.39.8"
     CDS             86..1126
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /note="isoform 2 is encoded by transcript variant 2;
                     LIM-homeodomain protein Lhx8; LIM/homeobox protein Lhx8"
                     /codon_start=1
                     /product="LIM/homeobox protein Lhx8 isoform 2"
                     /protein_id="NP_001243043.1"
                     /db_xref="GI:368711326"
                     /db_xref="CCDS:CCDS58008.1"
                     /db_xref="GeneID:431707"
                     /db_xref="HGNC:28838"
                     /db_xref="MIM:604425"
                     /translation="

MSEECGRTTALAAGRTRKGAGEEGLVSPEGAGDEDSCSSSAPLSPSSSPRSMASGSGCPPGKCVCNSCGLEIVDKYLLKVNDLCWHVRCLSCSVCRTSLGRHTSCYIKDKDIFCKLDYFRRYGTRCSRCGRHIHSTDWVRRAKGNVYHLACFACFSCKRQLSTGEEFALVEEKVLCRVHYDCMLDNLKREVENGNGISVEGALLTEQDVNHPKPAKRARTSFTADQLQVMQAQFAQDNNPDAQTLQKLAERTGLSRRVIQVWFQNCRARHKKHVSPNHSSSTPVTAVPPSRLSPPMLEEMAYSAYVPQDGTMLTALHSYMDAHSPTTLGLQPLLPHSMTQLPISHT

"
     misc_feature    275..442
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /note="The first LIM domain of Lhx7 and Lhx8; Region:
                     LIM1_Lhx7_Lhx8; cd09381"
                     /db_xref="CDD:188767"
     misc_feature    order(278..280,287..289,341..343,350..352,359..361,
                     368..370,425..427,434..436)
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /note="Zn binding site [ion binding]; other site"
                     /db_xref="CDD:188767"
     misc_feature    461..625
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /note="The second LIM domain of Lhx7 and Lhx8; Region:
                     LIM2_Lhx7_Lhx8; cd09383"
                     /db_xref="CDD:188769"
     misc_feature    order(461..463,470..472,527..529,536..538,545..547,
                     554..556,611..613,620..622)
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /note="Zn binding site [ion binding]; other site"
                     /db_xref="CDD:188769"
     misc_feature    731..904
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /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(731..745,749..751,800..802,818..820,857..859,
                     863..868,875..880,884..892,896..901)
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /note="DNA binding site [nucleotide binding]"
                     /db_xref="CDD:28970"
     misc_feature    order(737..739,746..748,866..868,875..880,887..889)
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /note="specific DNA base contacts [nucleotide binding];
                     other site"
                     /db_xref="CDD:28970"
     variation       86
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:116590034"
     variation       104
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376772505"
     variation       135
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:143612358"
     variation       145
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140847718"
     variation       156
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369761078"
     exon            161..322
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /inference="alignment:Splign:1.39.8"
     variation       166
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369347146"
     variation       177
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141641179"
     variation       183
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373338242"
     variation       202
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371247581"
     variation       205
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:145195318"
     variation       208
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371111953"
     variation       233
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:376300206"
     variation       298
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149422695"
     exon            323..444
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /inference="alignment:Splign:1.39.8"
     variation       327
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:373880349"
     variation       392
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:199843823"
     exon            445..665
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /inference="alignment:Splign:1.39.8"
     variation       459
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367958622"
     variation       475
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148556375"
     variation       481
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376834338"
     variation       491
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371719492"
     variation       496
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:12084309"
     variation       499
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:374741343"
     variation       655
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372110957"
     exon            666..769
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /inference="alignment:Splign:1.39.8"
     variation       667
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:376728766"
     variation       691
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147867930"
     exon            770..865
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /inference="alignment:Splign:1.39.8"
     exon            866..1049
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /inference="alignment:Splign:1.39.8"
     variation       868
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:79714503"
     variation       904
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:941032"
     variation       912
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200810970"
     variation       950
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:201945188"
     variation       955
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144728419"
     variation       958
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:375095039"
     variation       982
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:368509617"
     variation       1000
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370428970"
     variation       1001
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374046822"
     variation       1018
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145367581"
     variation       1029
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:34889650"
     exon            1050..1764
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /inference="alignment:Splign:1.39.8"
     variation       1097
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368782371"
     variation       1105
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:377005651"
     variation       1160
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:41306167"
     variation       1175
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199821156"
     variation       1177
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:41301265"
     variation       1224
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:184821578"
     variation       1321
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:187614610"
     variation       1399
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374351080"
     variation       1436
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:192190181"
     variation       1490
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142785057"
     variation       1543
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184182933"
     variation       1604
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147403016"
     variation       1690
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:190197837"
     variation       1702
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:4949795"
     polyA_signal    1732..1737
                     /gene="LHX8"
                     /gene_synonym="LHX7"
     variation       1743
                     /gene="LHX8"
                     /gene_synonym="LHX7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377666437"
     polyA_site      1764
                     /gene="LHX8"
                     /gene_synonym="LHX7"
ORIGIN      

ctcacttaacctgagacatggagactgtaatttgggagatgaagcctcgagcctaaggcgctctcaggtccattgtcaggggctcatgtcagaggagtgcgggcggactacagccctggcggccgggaggactcgcaaaggcgccggggaagagggactggtgagccccgagggagcgggggacgaggactcgtgctcctcctcggccccgctgtccccgtcgtcctcgccccggtccatggcctcgggctccggctgccctcctggcaagtgtgtgtgcaacagttgcggcctggagatcgtggacaaataccttctcaaggtgaatgacctatgctggcatgtccggtgtctctcctgcagtgtttgcagaacctccctaggaaggcacaccagctgttatattaaagacaaagacattttctgcaaacttgattatttcagaaggtatggaactcgctgctctcgatgtgggagacacatccattctactgactgggtccggagagccaaggggaatgtctatcacttggcatgctttgcctgcttttcctgcaaaaggcaactttccacaggagaggagtttgctttggtggaagagaaagtcctctgcagagtacattatgactgcatgctggataatttaaaaagagaagtagaaaatgggaatgggattagtgtggaaggtgccctcctcacagagcaagatgttaaccatccaaaaccagcaaaaagagctcggaccagctttacagcagatcagcttcaggttatgcaagcacaatttgctcaggacaacaacccagatgcacagacactccagaaattggcagaaaggacaggcttgagcagacgtgtgatacaggtgtggtttcagaattgtagagcacgccacaagaaacacgtcagtcctaatcactcatcctccaccccagtcacagcagtcccaccctccaggctgtctccacccatgttagaagaaatggcttattctgcctacgtgccccaagatggaacgatgttaactgcgctgcatagttatatggatgctcattcaccaacaactcttggactccagcccttgttaccccattcaatgacacaactgccaataagtcatacctaattcttttttcagggatagacttgattaaggatataaatttgtcatttattatgtataaaataccattgaaaagatattactgttaattttttatttaacacctaaagcatttccaacatcactttgctgcccaggtatgtatctatagttggcctgcaagacacttttattaattcttcattttttgtaaaacttatgtttacaagaagaaaacaaatcaaaacattttttgtattgtctggaaatagttcactctagtgtgtatctgttaatttatttgtcatcaaaagagcactttgcctaaaagaaaggactgacaagtgtgcaaaatgtttacaatcttttgtgaaattgtagtttatcattagtttgtatctgtaagttattgtaataaatattacctgtattttttgttatatacaactttatactttgaagcttgtatctgtgaatttgcaactgaaatttattttgccaatgttttctgaatgaactgaataaagcttctgttgtagcatgccatgcaaacacattattgtgtttgtggttgatgaattatggctgtaaataacactatagtttaataagcccaccattctgagtttattaaacattttccattcttgtgaaaatttcaaaaaaaaaaaaaaaaaaaaaa

//

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:431707 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: IEA
            GeneID:431707 -> Molecular function: GO:0008270 [zinc ion binding] evidence: IEA
            GeneID:431707 -> Molecular function: GO:0043565 [sequence-specific DNA binding] evidence: IEA
            GeneID:431707 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IEA
            GeneID:431707 -> Biological process: GO:0007611 [learning or memory] evidence: IEA
            GeneID:431707 -> Biological process: GO:0008585 [female gonad development] evidence: IEA
            GeneID:431707 -> Biological process: GO:0021884 [forebrain neuron development] evidence: IEA
            GeneID:431707 -> Biological process: GO:0042475 [odontogenesis of dentin-containing tooth] evidence: IEA
            GeneID:431707 -> Cellular component: GO:0005634 [nucleus] evidence: IEA