LOCUS       NM_001174146            5816 bp    mRNA    linear   PRI 15-JUN-2013
DEFINITION  Homo sapiens LIM homeobox transcription factor 1, beta (LMX1B),
            transcript variant 3, mRNA.
ACCESSION   NM_001174146
VERSION     NM_001174146.1  GI:292494912
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 5816)
  AUTHORS   Zhou,T.B. and Qin,Y.H.
  TITLE     The signaling pathways of LMX1B and its role in glomerulosclerosis
  JOURNAL   J. Recept. Signal Transduct. Res. 32 (6), 285-289 (2012)
   PUBMED   23046462
  REMARK    GeneRIF: LMX1B is important in regulating type IV collagen gene
            expression in the GBM of the developing kidney and also has a
            likely role in regulating additional genes important in podocyte
            function and maintenance
            Review article
REFERENCE   2  (bases 1 to 5816)
  AUTHORS   Thanseem,I., Nakamura,K., Anitha,A., Suda,S., Yamada,K.,
            Iwayama,Y., Toyota,T., Tsujii,M., Iwata,Y., Suzuki,K.,
            Matsuzaki,H., Iwata,K., Sugiyama,T., Yoshikawa,T. and Mori,N.
  TITLE     Association of transcription factor gene LMX1B with autism
  JOURNAL   PLoS ONE 6 (8), E23738 (2011)
   PUBMED   21901133
  REMARK    GeneRIF: Data report on the association of LMX1B with autism,
            though it should be viewed with some caution considering the modest
            associations we report.
REFERENCE   3  (bases 1 to 5816)
  AUTHORS   Romero,P., Sanhueza,F., Lopez,P., Reyes,L. and Herrera,L.
  TITLE     c.194 A>C (Q65P) mutation in the LMX1B gene in patients with
            nail-patella syndrome associated with glaucoma
  JOURNAL   Mol. Vis. 17, 1929-1939 (2011)
   PUBMED   21850167
  REMARK    GeneRIF: c.194 A>C (Q65P) mutation is present in the LMX1B gene of
            the Chilean patients with nail-patella syndrome associated with
            glaucoma.
REFERENCE   4  (bases 1 to 5816)
  AUTHORS   Song,N.N., Xiu,J.B., Huang,Y., Chen,J.Y., Zhang,L., Gutknecht,L.,
            Lesch,K.P., Li,H. and Ding,Y.Q.
  TITLE     Adult raphe-specific deletion of Lmx1b leads to central serotonin
            deficiency
  JOURNAL   PLoS ONE 6 (1), E15998 (2011)
   PUBMED   21246047
  REMARK    GeneRIF: effect of lmx1b on gene expression regulation in the brain
            Publication Status: Online-Only
REFERENCE   5  (bases 1 to 5816)
  AUTHORS   Dunston,J.A., Hamlington,J.D., Zaveri,J., Sweeney,E., Sibbring,J.,
            Tran,C., Malbroux,M., O'Neill,J.P., Mountford,R. and McIntosh,I.
  TITLE     The human LMX1B gene: transcription unit, promoter, and pathogenic
            mutations
  JOURNAL   Genomics 84 (3), 565-576 (2004)
   PUBMED   15498463
REFERENCE   6  (bases 1 to 5816)
  AUTHORS   Vollrath,D., Jaramillo-Babb,V.L., Clough,M.V., McIntosh,I.,
            Scott,K.M., Lichter,P.R. and Richards,J.E.
  TITLE     Loss-of-function mutations in the LIM-homeodomain gene, LMX1B, in
            nail-patella syndrome
  JOURNAL   Hum. Mol. Genet. 7 (7), 1091-1098 (1998)
   PUBMED   9618165
  REMARK    Erratum:[Hum Mol Genet 1998 Aug;7(8):1333]
REFERENCE   7  (bases 1 to 5816)
  AUTHORS   Chen,H., Lun,Y., Ovchinnikov,D., Kokubo,H., Oberg,K.C.,
            Pepicelli,C.V., Gan,L., Lee,B. and Johnson,R.L.
  TITLE     Limb and kidney defects in Lmx1b mutant mice suggest an involvement
            of LMX1B in human nail patella syndrome
  JOURNAL   Nat. Genet. 19 (1), 51-55 (1998)
   PUBMED   9590288
REFERENCE   8  (bases 1 to 5816)
  AUTHORS   Dreyer,S.D., Zhou,G., Baldini,A., Winterpacht,A., Zabel,B.,
            Cole,W., Johnson,R.L. and Lee,B.
  TITLE     Mutations in LMX1B cause abnormal skeletal patterning and renal
            dysplasia in nail patella syndrome
  JOURNAL   Nat. Genet. 19 (1), 47-50 (1998)
   PUBMED   9590287
REFERENCE   9  (bases 1 to 5816)
  AUTHORS   Iannotti,C.A., Inoue,H., Bernal,E., Aoki,M., Liu,L.,
            Donis-Keller,H., German,M.S. and Permutt,M.A.
  TITLE     Identification of a human LMX1 (LMX1.1)-related gene, LMX1.2:
            tissue-specific expression and linkage mapping on chromosome 9
  JOURNAL   Genomics 46 (3), 520-524 (1997)
   PUBMED   9441763
REFERENCE   10 (bases 1 to 5816)
  AUTHORS   Johnson,J.D., Zhang,W., Rudnick,A., Rutter,W.J. and German,M.S.
  TITLE     Transcriptional synergy between LIM-homeodomain proteins and basic
            helix-loop-helix proteins: the LIM2 domain determines specificity
  JOURNAL   Mol. Cell. Biol. 17 (7), 3488-3496 (1997)
   PUBMED   9199284
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from AL161908.13, BC143801.1,
            AL161731.20 and EL952935.1.
            
            Summary: This gene encodes a member of LIM-homeodomain family of
            proteins containing two N-terminal zinc-binding LIM domains, 1
            homeodomain, and a C-terminal glutamine-rich domain. It functions
            as a transcription factor, and is essential for the normal
            development of dorsal limb structures, the glomerular basement
            membrane, the anterior segment of the eye, and dopaminergic and
            serotonergic neurons. Mutations in this gene are associated with
            nail-patella syndrome. Alternatively spliced transcript variants
            encoding different isoforms have been found for this gene.
            [provided by RefSeq, Mar 2010].
            
            Transcript Variant: This variant (3) uses an alternate donor splice
            site at an internal coding exon compared to variant 1, resulting in
            a longer isoform (3) containing an additional 11 aa protein segment
            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 :: BC143801.1 [ECO:0000332]
            RNAseq introns              :: mixed/partial sample support
                                           ERS025088 [ECO:0000350]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-26                AL161908.13        64452-64477
            27-1326             BC143801.1         1-1300
            1327-5426           AL161731.20        40443-44542
            5427-5816           EL952935.1         44-433
FEATURES             Location/Qualifiers
     source          1..5816
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="9"
                     /map="9q33.3"
     gene            1..5816
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /note="LIM homeobox transcription factor 1, beta"
                     /db_xref="GeneID:4010"
                     /db_xref="HGNC:6654"
                     /db_xref="MIM:602575"
     exon            1..146
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /inference="alignment:Splign:1.39.8"
     CDS             8..1228
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /note="isoform 3 is encoded by transcript variant 3;
                     LMX-1.2; LIM/homeobox protein 1.2; LIM/homeobox protein
                     LMX1B"
                     /codon_start=1
                     /product="LIM homeobox transcription factor 1-beta isoform
                     3"
                     /protein_id="NP_001167617.1"
                     /db_xref="GI:292494913"
                     /db_xref="CCDS:CCDS55343.1"
                     /db_xref="GeneID:4010"
                     /db_xref="HGNC:6654"
                     /db_xref="MIM:602575"
                     /translation="

MDIATGPESLERCFPRGQTDCAKMLDGIKMEEHALRPGPATLGVLLGSDCPHPAVCEGCQRPISDRFLMRVNESSWHEECLQCAACQQALTTSCYFRDRKLYCKQDYQQLFAAKCSGCMEKIAPTEFVMRALECVYHLGCFCCCVCERQLRKGDEFVLKEGQLLCKGDYEKEKDLLSSVSPDESDSVKSEDEDGDMKPAKGQGSQSKGSGDDGKDPRRPKRPRTILTTQQRRAFKASFEVSSKPCRKVRETLAAETGLSVRVVQVWFQNQRAKMKKLARRHQQQQEQQNSQRLGQGEPGPGQGLGQEVLSSRMEGMMASYTPLAPPQQQIVAMEQSPYGSSDPFQQGLTPPQMPGNDSIFHDIDSDTSLTSLSDCFLGSSDVGSLQARVGNPIDRLYSMQSSYFAS

"
     misc_feature    173..331
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /note="The first LIM domain of Lmx1b; Region: LIM1_Lmx1b;
                     cd09371"
                     /db_xref="CDD:188757"
     misc_feature    order(173..175,182..184,236..238,245..247,254..256,
                     263..265,314..316,323..325)
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /note="Zn binding site [ion binding]; other site"
                     /db_xref="CDD:188757"
     misc_feature    350..514
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /note="The second LIM domain of Lmx1a and Lmx1b; Region:
                     LIM2_Lmx1a_Lmx1b; cd09378"
                     /db_xref="CDD:188764"
     misc_feature    order(350..352,359..361,416..418,425..427,434..436,
                     443..445,500..502,509..511)
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /note="Zn binding site [ion binding]; other site"
                     /db_xref="CDD:188764"
     misc_feature    677..835
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /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(677..679,683..685,734..736,752..754,791..793,
                     797..802,809..814,818..826,830..835)
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /note="DNA binding site [nucleotide binding]"
                     /db_xref="CDD:28970"
     misc_feature    order(680..682,800..802,809..814,821..823)
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /note="specific DNA base contacts [nucleotide binding];
                     other site"
                     /db_xref="CDD:28970"
     STS             27..1326
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /db_xref="UniSTS:483257"
     variation       64
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376265443"
     STS             77..1228
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /db_xref="UniSTS:480873"
     variation       108
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:375095510"
     variation       123
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367661538"
     exon            147..333
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /inference="alignment:Splign:1.39.8"
     variation       157
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148305192"
     variation       168
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371819068"
     variation       191
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371293980"
     variation       217
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:374685767"
     variation       231
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:2235058"
     variation       251
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:121909489"
     variation       258
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377436751"
     variation       259
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:2235059"
     variation       302
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:141391682"
     exon            334..566
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /inference="alignment:Splign:1.39.8"
     variation       340
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138385790"
     variation       342
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370537843"
     variation       343
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144043214"
     variation       360
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:121909488"
     variation       373
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200350302"
     variation       376
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:147293594"
     variation       379
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374078636"
     variation       399
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373429181"
     variation       400
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:190161633"
     variation       439
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375657880"
     variation       448
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2277158"
     variation       458
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149434820"
     variation       514
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368298608"
     variation       515
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199738980"
     variation       541
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:116316477"
     variation       542
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:181422024"
     variation       549
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:148403563"
     variation       550
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375486982"
     variation       553
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:34434402"
     variation       559
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142488434"
     variation       565
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370299750"
     exon            567..748
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /inference="alignment:Splign:1.39.8"
     variation       598
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146465341"
     variation       601
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139862413"
     variation       668
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:121909487"
     variation       673
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143407067"
     variation       675
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:121909491"
     variation       676
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146720578"
     variation       688
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147071667"
     variation       698
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:121909490"
     variation       730
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368736494"
     variation       733
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:13295990"
     exon            749..826
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /inference="alignment:Splign:1.39.8"
     variation       752
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:121909492"
     variation       790
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371560611"
     variation       814
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:121909486"
     exon            827..926
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /inference="alignment:Splign:1.39.8"
     variation       921
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150656317"
     exon            927..1070
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /inference="alignment:Splign:1.39.8"
     variation       934
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373033856"
     variation       941
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376497496"
     variation       969
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369831428"
     variation       970
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112171815"
     variation       973
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:145052881"
     variation       1022
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373336352"
     variation       1054
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199580468"
     exon            1071..5809
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /inference="alignment:Splign:1.39.8"
     variation       1078
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148940265"
     variation       1080
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147035553"
     variation       1125
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:76277667"
     variation       1126
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:10115304"
     variation       1127
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:78770531"
     variation       1151
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375881049"
     variation       1169
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367916653"
     variation       1170
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143906016"
     variation       1171
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146476348"
     variation       1183
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148356178"
     variation       1190
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141496559"
     variation       1192
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200484654"
     variation       1219
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372183654"
     variation       1241
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375458623"
     variation       1249
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369706326"
     variation       1255
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:10115373"
     variation       1266
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201442685"
     variation       1267
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:376851692"
     variation       1268
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374778848"
     variation       1279
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:10121481"
     variation       1307
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:10115393"
     variation       1355
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:113846301"
     variation       1383
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:151191848"
     variation       1401
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:181701033"
     variation       1482
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371380792"
     variation       1508
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:111648919"
     variation       1666
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:140325479"
     variation       1679
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:71497630"
     variation       1705
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374016635"
     variation       1743
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112375232"
     variation       1812
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:34200683"
     variation       1861..1864
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace=""
                     /replace="acac"
                     /db_xref="dbSNP:147813553"
     variation       1909
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138360048"
     variation       1936
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:10987413"
     variation       1976
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:10987414"
     variation       2013
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143919006"
     variation       2112
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146268507"
     variation       2126
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:10760450"
     variation       2160
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:28687510"
     variation       2163
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:186360995"
     variation       2228
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:189691069"
     variation       2334..2335
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace=""
                     /replace="tt"
                     /db_xref="dbSNP:201556524"
     variation       2359
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138749439"
     variation       2378
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:181187127"
     variation       2418
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374742119"
     variation       2468..2469
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace=""
                     /replace="tg"
                     /db_xref="dbSNP:368812241"
     variation       2468
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:368887101"
     variation       2483
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:16929236"
     variation       2532
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:73596779"
     variation       2556
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:185183718"
     variation       2615..2619
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace=""
                     /replace="tgttt"
                     /db_xref="dbSNP:67078890"
     variation       2615..2616
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace=""
                     /replace="g"
                     /replace="tgttt"
                     /db_xref="dbSNP:72111206"
     variation       2617
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:13300385"
     variation       2617
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="gtttt"
                     /replace="ttttg"
                     /db_xref="dbSNP:71493852"
     variation       2620..2644
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace=""
                     /replace="tgttttgttttgttttgttttgttt"
                     /db_xref="dbSNP:370075271"
     variation       2621
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:200514771"
     variation       2621
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:13299451"
     variation       2665
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace=""
                     /replace="tgttt"
                     /db_xref="dbSNP:10581734"
     variation       2669..2670
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace=""
                     /replace="tgttt"
                     /db_xref="dbSNP:59836255"
     variation       2701
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:13299609"
     STS             2719..2928
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /standard_name="RH80030"
                     /db_xref="UniSTS:87680"
     variation       2722
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370649232"
     variation       2738
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:189648333"
     variation       2747
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:183329572"
     variation       2766
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:144857145"
     variation       2802
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:148173186"
     variation       2810
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:10987415"
     variation       2832
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146126278"
     variation       2866..2886
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace=""
                     /replace="ggtctccaacccccgacctca"
                     /db_xref="dbSNP:199608526"
     variation       2872
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:187256465"
     variation       2894
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:10987416"
     variation       2895
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375078942"
     variation       2901
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:191584459"
     variation       2931
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144070517"
     variation       2944
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:116411474"
     variation       2988
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:183486611"
     variation       3015
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372210078"
     variation       3220..3225
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="ccccaa"
                     /replace="tcccag"
                     /db_xref="dbSNP:71494050"
     variation       3220
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:34776870"
     variation       3223
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:74498940"
     variation       3225
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:35632228"
     variation       3388
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145937520"
     variation       3412
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:10733682"
     variation       3422..3423
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:149174535"
     variation       3573
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:74429080"
     variation       3613
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:35712948"
     variation       3621
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:10120414"
     variation       3622
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:10760451"
     variation       3659
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:114971128"
     variation       3685
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:188331536"
     variation       3691
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:373410299"
     variation       3761
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376612764"
     variation       3809
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:370880644"
     variation       3815
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374778359"
     variation       3817..3818
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace=""
                     /replace="tt"
                     /db_xref="dbSNP:35559677"
     variation       3818
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:77350418"
     variation       3819
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace=""
                     /replace="tt"
                     /db_xref="dbSNP:57949927"
     variation       3941
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139482215"
     variation       3942
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149740102"
     variation       3967
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:145602359"
     variation       4059
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148906444"
     variation       4194
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:191951894"
     variation       4212
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:4083644"
     variation       4410
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:3861878"
     variation       4476
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:145190620"
     variation       4570
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:4083645"
     variation       4574
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:7023938"
     variation       4782
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:182607285"
     variation       4787
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376141195"
     variation       4944
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:147614955"
     variation       4999
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:10987417"
     variation       5061
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:10987418"
     variation       5092
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:10987419"
     variation       5093
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:10987420"
     variation       5109
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:10987421"
     variation       5185
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:10987422"
     variation       5208
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:186932324"
     variation       5355
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146636393"
     variation       5357
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148294658"
     variation       5358
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140459665"
     variation       5385
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:185290341"
     variation       5393
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:111940190"
     variation       5399
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:3814119"
     variation       5438
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:374547564"
     variation       5516
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150407176"
     variation       5601
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:78565800"
     variation       5765
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:78799000"
     polyA_signal    5789..5794
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
     variation       5798..5799
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:35956748"
     polyA_site      5809
                     /gene="LMX1B"
                     /gene_synonym="LMX1.2; NPS1"
ORIGIN      

gcgtcccatggatatagcaacaggtcccgagtcgctggagaggtgcttccctcgcgggcagacggactgcgccaagatgttggacggcatcaagatggaggagcacgccctgcgccccgggcccgccactctgggggtgctgctgggctccgactgcccgcatcccgccgtctgcgagggctgccagcggcccatctccgaccgcttcctgatgcgagtcaacgagtcgtcctggcacgaggagtgtttgcagtgcgcggcgtgtcagcaagccctcaccaccagctgctacttccgggatcggaaactgtactgcaaacaagactaccaacagctcttcgcggccaagtgcagcggctgcatggagaagatcgcccccaccgagttcgtgatgcgggcgctggagtgcgtgtaccacctgggctgcttctgctgctgcgtgtgtgaacggcagctacgcaagggcgacgaattcgtgctcaaggagggccagctgctgtgcaagggtgactacgagaaggagaaggacctgctcagctccgtgagccccgacgagtccgactccgtgaagagcgaggatgaagatggggacatgaagccggccaaggggcagggcagtcagagcaagggcagcggggatgacgggaaggacccgcggaggcccaagcgaccccggaccatcctcaccacgcagcagcgaagagccttcaaggcctccttcgaggtctcgtcgaagccttgccgaaaggtccgagagacactggcagctgagacgggcctcagtgtgcgcgtggtccaggtctggtttcagaaccaaagagcaaagatgaagaagctggcgcggcggcaccagcagcagcaggagcagcagaactcccagcggctgggccagggtgagccggggccggggcagggcctgggccaggaggtcctgtccagccgcatggagggcatgatggcttcctacacgccgctggccccaccacagcagcagatcgtggccatggaacagagcccctacggcagcagcgaccccttccagcagggcctcacgccgccccaaatgccagggaacgactccatcttccatgacatcgacagcgatacctccttaaccagcctcagcgactgcttcctcggctcctcagacgtgggctccctgcaggcccgcgtggggaaccccatcgaccggctctactccatgcagagttcctacttcgcctcctgagagccagccaggcgcacggacgcttgggcaggggcctgggggggactgccagcctctgcggccagcctggccacccccgccctgctctccgcacagactacagacagccatacggtgccctcccctcggccagctgggcctgaccactgtgcccgttgggtacagccagaccggtagatgggcacagcctgggcaggggctgtgtcctgcccacagagaccttgtcatccccagggacccagagctctcggacggccactcgcctcccagccccacctcggcctccatcgcctcctccccatctcttttttgggaagcttaaattctctctatttttttaaatgtcctctctgtgtccatggccctccatgcaagccccaggacaatggtgtcatgaggcggtgacctgagaagcgtgtgtacctgtgccccagcaagggcaggggtggcctctgggggcaggcccactgcctggaaccgcacacccctcagcctgagtctggagcagcagtggagaggggcctgaggggaggcactgtcaggaggcgggctcggagcctgagcctgggcaggcgcaaagggacagagaggcacgtgcagacacatgcacacttgcagacaaacccacgcaaacacacacacagctgtatggggacaccagaagggacagggatgctcagcgggtctgtcctgccttgtcagaaagagaaaaggaggccaggcaggggaccccccagttcttaagagcgattggaaagggaggaaggggagaggaagaggcgaacttgaagcatcggacccagttgtatcccagcctgggcccaaatgggggcagcctgggcagggagggcagccccaggccccaccaactctagaggcagatggagcccccagaaccaggtagcatcagaccagacaacagagcctccaggggtcagggacttcagaagcacctgctgggcaccccatctgcaatgtggtcctctccccagccacctctgcctcccctcacatacctccagtgacaaggagctcactaggtcagcgagcccacagcagctgtgctgtcctgcatcccagagccaggcttccccagctctccctcttaacactgtcccccagcaggcctccggctgtccctctaaaggtgtggggcaggtatcacttcaccttcccactgatgtcagccggccagaagtgagcaggcacatcacctctcctgctgtggcacccttcctctgttaatttggcccaaaagacaatgatttggccacatgaccttagagattcaccctgccctgctgtagctaaatccctgggccccacacgcaagtgacagctaagccacatctgttttctgtgtatatgcaggatgggggcacctactgttttgttttgttttgttttgttttgttttgttttgttttgttttgttttgtttgagacggagtttcgctcttgttgcccaggctggagtgcaatggcgcgatctcggctcaccacaacctccgcctcccaggttcaagtgattctgatgcctcagcctccctagtagctgagattacaggcatgcgccaccacacccagctaattttgtatttttagtagcaacggggtttctccatgttggtcaggctggtctccaacccccgacctcaggtgatccgcctgcctcggcctcccaaagtgctgggattacaggcgtgagccaccgcacccagtctgcacttactgtttagactgaatgagggaccgtgacctctttccttttccattccttcttactcgattcattccagcctgtggaatttctctgcaccctgattcagtgaccactgctctcctctctcccagcacatctgcccagtgaggagttggccctgggtctcacctgaggtgtgtggaccgggctggcctctccctgtttgacattggcccattaatgcatcctctttgggggacacattccaattgcatttcctgcccccttctcccagggcaattgcagaagattgtgtcaggcgccctgctggaagtcaggtgcactagatccatccccagccccagtctgctcaactctatccctgtcagagcaaggaggctgggctgctggggcctgactggtgagcccaccctgtcccctggtgatcactgtgtccccttgttcaggtgctcacaaccctacctttaactctgaggtcaagccctaggccaccaccctaaagtctgcctggtccaacctttgagcaagtaaggataatgaatgtcccttttccacctttggggccctctgcctggatctctggaatcctctaagttcaacctgttctgtggttttgctcccgtttgctgggaaattcagtccccccagaatgtcctgggccaacctccttgcctgacatgtggcctcgtgtcacccattgggccccagcagccagctagcccttctgcagctcttcttacaaacagagcctctccaaggacctcagttgatgttctggtccttctgccgcctcagcccaccagggtccgtgccaccatgggtctcttgagcagcagctgcactggcttctggagagacacccctctttctccttttgcacatgcaccatctgaatcgtgccagggacatcctgggcagattcaggggcagatgccctatcccccaggagacctggcccttctctctcagacccaataagttggaagggacgtcagaagcggtcatctcatctgccccttattttatagttggaaaccctgaggcaagagagggaaagaggcctgtccaaggtccgggttagtgacagagctgagctgagaacagggacgttgtgccccactgtcccctgtggtttgtgaatgacctccaggtcagggggtcacaacttgttcttagtaaacttgccagctgttggggtcacatattcccattctggggcctcacaaacccccgaatccagccgggaccccatgccaggagctggtctagggacagcatgcttgtgacccacagactgttaaagccagaagggacctcagagagtcccttatgctggaggcgccctgtcagccgtggctaggggccccttgctctatgctgtgccttgctgcccacaggctcccagacaccagtgcccactctgcccagccccggactgggtgtggctcgcagatgaacaagatgcagggcctgccttgaggggtgtctcctagaaggaaagccagactctccggcccagccagagagtccagacatggcagggacccgtttctcagatgaggagcctgaggctcagagaagggaggcgatgtgttcagggccacccagcagaagcctgtggggctgggcaaccttctcccactttatgggaggagctgcagccttggctgggagctgggcggggagtagccaggaccaccccttgcccgtgccgtgacatggaaccttcatcactaagggggctggagtgggaagagggagataactgtgtggtctccagagcaaaagagaatgagaggtgggcagggggagtcttggcaaaagaccaagttccacttccctgctggggaagtcaaggctcagaaagaggaaataattgccccaggtaacacagggcagaggagggacaaaaagctgggcatggccccagccagagcctcatctgcctactccgtgaagcctcccaggtactctgctatcctgggaaacgcacagggaggccacacagagacactgctcacaagagtcagaccaaggtgccagcacagcctggaaagagctcagaaagggggttggtgcacgtggctgggcatcttaggaggcttcctgagggtgggtaaaggtgggaaggccctggcgctgcatcagatgagcagggcctggcagggacaagcctcttctcctttgggaagccctgcagcctcctagcaagaggctgattccccactctgcccccatctgaatgtccttttcatgttgcacgcagggaacctcaggaaggaggattgcctgatgcctgcctggctccatccttgagctctgggcaccacctagggtgagggagagcctgcagctctggggctaagtctgccctggggggaaagggctccacgctcacacgcacgcgctcgcacacacacactcacacctggacgcacacggaggcttgcggacccatactcacaggcacatgtggcctggggactgggggagcaggaaagacccctccaacatttggcccttggaaggcaccattgccaatgagcctctttgctggttcccccgaccccacctgggggtcccatgggagcccagcccagccaggtgtggggatgggccaccggccattcctgttttccttgtacagacagattctcactacccacccgccatccccagacacattttatttaataacttgtcattgttaaattatttattagcgtttaccacaccaccacccccaccctgccctccactctcaccttccacctcttcccacaacagcagaaaatggaaacaacaacaaaaaaagatgagacatcagtatatttgtaaataaaccgacctgtacactcaaaaaaa

//

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:4010 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: IDA
            GeneID:4010 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
            GeneID:4010 -> Molecular function: GO:0008270 [zinc ion binding] evidence: IEA
            GeneID:4010 -> Molecular function: GO:0043565 [sequence-specific DNA binding] evidence: IEA
            GeneID:4010 -> Biological process: GO:0001701 [in utero embryonic development] evidence: NAS
            GeneID:4010 -> Biological process: GO:0001764 [neuron migration] evidence: IEA
            GeneID:4010 -> Biological process: GO:0002930 [trabecular meshwork development] evidence: IEA
            GeneID:4010 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IEA
            GeneID:4010 -> Biological process: GO:0006355 [regulation of transcription, DNA-dependent] evidence: IDA
            GeneID:4010 -> Biological process: GO:0007275 [multicellular organismal development] evidence: NAS
            GeneID:4010 -> Biological process: GO:0008219 [cell death] evidence: IEA
            GeneID:4010 -> Biological process: GO:0008283 [cell proliferation] evidence: IEA
            GeneID:4010 -> Biological process: GO:0009953 [dorsal/ventral pattern formation] evidence: ISS
            GeneID:4010 -> Biological process: GO:0021587 [cerebellum morphogenesis] evidence: IEA
            GeneID:4010 -> Biological process: GO:0021954 [central nervous system neuron development] evidence: IEA
            GeneID:4010 -> Biological process: GO:0030182 [neuron differentiation] evidence: ISS
            GeneID:4010 -> Biological process: GO:0030199 [collagen fibril organization] evidence: IEA
            GeneID:4010 -> Biological process: GO:0030901 [midbrain development] evidence: IEA
            GeneID:4010 -> Biological process: GO:0035108 [limb morphogenesis] evidence: IEA
            GeneID:4010 -> Biological process: GO:0035265 [organ growth] evidence: IEA
            GeneID:4010 -> Biological process: GO:0045944 [positive regulation of transcription from RNA polymerase II promoter] evidence: IEA
            GeneID:4010 -> Biological process: GO:0071542 [dopaminergic neuron differentiation] evidence: IEA
            GeneID:4010 -> Cellular component: GO:0005634 [nucleus] evidence: IDA