2024-04-26 07:26:09, GGRNA : RefSeq release 60 (20130726)
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
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