2025-05-09 20:09:38, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001174069 3366 bp mRNA linear PRI 21-APR-2013 DEFINITION Homo sapiens LIM homeobox transcription factor 1, alpha (LMX1A), transcript variant 4, mRNA. ACCESSION NM_001174069 VERSION NM_001174069.1 GI:291327512 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 3366) AUTHORS Tsai,W.C., Lee,H.S., Lin,C.K., Chen,A., Nieh,S. and Ma,H.I. TITLE The association of osteopontin and LMX1A expression with World Health Organization grade in meningiomas and gliomas JOURNAL Histopathology 61 (5), 844-856 (2012) PUBMED 22882568 REMARK GeneRIF: Higher immunostaining intensity for OPN and LMX1A correlated with WHO grades for meningiomas and some gliomas. Contrary to our expectations, LMX1A staining in WHO grade IV gliomas was shown to be weaker than in WHO grade III tumours. REFERENCE 2 (bases 1 to 3366) AUTHORS Panman,L., Andersson,E., Alekseenko,Z., Hedlund,E., Kee,N., Mong,J., Uhde,C.W., Deng,Q., Sandberg,R., Stanton,L.W., Ericson,J. and Perlmann,T. TITLE Transcription factor-induced lineage selection of stem-cell-derived neural progenitor cells JOURNAL Cell Stem Cell 8 (6), 663-675 (2011) PUBMED 21624811 REMARK GeneRIF: The Lmx1a can induce desired neuronal lineages from most expressing neural progenitor cells by a mechanism resembling developmental binary cell-fate switching. REFERENCE 3 (bases 1 to 3366) AUTHORS Bellander,M., Brehmer,Y., Westerberg,H., Karlsson,S., Furth,D., Bergman,O., Eriksson,E. and Backman,L. TITLE Preliminary evidence that allelic variation in the LMX1A gene influences training-related working memory improvement JOURNAL Neuropsychologia 49 (7), 1938-1942 (2011) PUBMED 21435346 REMARK GeneRIF: One single nucleotide polymorphisms of lmx1a was strongly associated with the magnitude of training-related gains in verbal working memory REFERENCE 4 (bases 1 to 3366) AUTHORS Moyer,A.M., Fridley,B.L., Jenkins,G.D., Batzler,A.J., Pelleymounter,L.L., Kalari,K.R., Ji,Y., Chai,Y., Nordgren,K.K. and Weinshilboum,R.M. TITLE Acetaminophen-NAPQI hepatotoxicity: a cell line model system genome-wide association study JOURNAL Toxicol. Sci. 120 (1), 33-41 (2011) PUBMED 21177773 REFERENCE 5 (bases 1 to 3366) AUTHORS Thameem,F., Wolford,J.K., Wang,J., German,M.S., Bogardus,C. and Prochazka,M. TITLE Cloning, expression and genomic structure of human LMX1A, and variant screening in Pima Indians JOURNAL Gene 290 (1-2), 217-225 (2002) PUBMED 12062816 REMARK GeneRIF: Did not find evidence for association of any LMX1A SNPs with type 2 diabetes mellitus (T2DM) and conclude that LMX1A does not contribute significantly to T2DM etiology in Pima Indians. GeneRIF: Observational study of gene-disease association. (HuGE Navigator) REFERENCE 6 (bases 1 to 3366) AUTHORS Jurata,L.W., Pfaff,S.L. and Gill,G.N. TITLE The nuclear LIM domain interactor NLI mediates homo- and heterodimerization of LIM domain transcription factors JOURNAL J. Biol. Chem. 273 (6), 3152-3157 (1998) PUBMED 9452425 REFERENCE 7 (bases 1 to 3366) 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 8 (bases 1 to 3366) AUTHORS Jurata,L.W. and Gill,G.N. TITLE Functional analysis of the nuclear LIM domain interactor NLI JOURNAL Mol. Cell. Biol. 17 (10), 5688-5698 (1997) PUBMED 9315627 REFERENCE 9 (bases 1 to 3366) AUTHORS German,M.S., Wang,J., Fernald,A.A., Espinosa,R. III, Le Beau,M.M. and Bell,G.I. TITLE Localization of the genes encoding two transcription factors, LMX1 and CDX3, regulating insulin gene expression to human chromosomes 1 and 13 JOURNAL Genomics 24 (2), 403-404 (1994) PUBMED 7698771 REFERENCE 10 (bases 1 to 3366) AUTHORS German,M.S., Wang,J., Chadwick,R.B. and Rutter,W.J. TITLE Synergistic activation of the insulin gene by a LIM-homeo domain protein and a basic helix-loop-helix protein: building a functional insulin minienhancer complex JOURNAL Genes Dev. 6 (11), 2165-2176 (1992) PUBMED 1358758 COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AL160058.8, AK122800.1, AK127724.1, AL390730.12 and BM678780.1. Summary: This gene encodes a homeodomain and LIM-domain containing protein. The encoded protein is a transcription factor that acts as a positive regulator of insulin gene transcription. This gene also plays a role in the development of dopamine producing neurons during embryogenesis. Mutations in this gene are associated with an increased risk of developing Parkinson's disease. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2012]. Transcript Variant: This variant (4) differs in the 5' UTR compared to variant 1. Both variants 1 and 4 encode the same protein. 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 :: AK122800.1 [ECO:0000332] RNAseq introns :: mixed/partial sample support ERS025085 [ECO:0000350] ##Evidence-Data-END## PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-3 AL160058.8 14906-14908 c 4-452 AK122800.1 4-452 453-1243 AK127724.1 642-1432 1244-1244 AL390730.12 11526-11526 c 1245-2420 AK127724.1 1434-2609 2421-2421 AK122800.1 2421-2421 2422-2785 AK127724.1 2610-2973 2786-3366 BM678780.1 8-588 c FEATURES Location/Qualifiers source 1..3366 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="1" /map="1q24.1" gene 1..3366 /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /note="LIM homeobox transcription factor 1, alpha" /db_xref="GeneID:4009" /db_xref="HGNC:6653" /db_xref="MIM:600298" exon 1..172 /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /inference="alignment:Splign:1.39.8" variation complement(88) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:72687734" exon 173..270 /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /inference="alignment:Splign:1.39.8" variation complement(179) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="g" /db_xref="dbSNP:368923297" variation complement(190) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:375965709" CDS 195..1343 /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /note="LIM/homeobox protein 1.1" /codon_start=1 /product="LIM homeobox transcription factor 1-alpha" /protein_id="NP_001167540.1" /db_xref="GI:291327513" /db_xref="CCDS:CCDS1247.1" /db_xref="GeneID:4009" /db_xref="HGNC:6653" /db_xref="MIM:600298" /translation="
MLDGLKMEENFQSAIDTSASFSSLLGRAVSPKSVCEGCQRVILDRFLLRLNDSFWHEQCVQCASCKEPLETTCFYRDKKLYCKYDYEKLFAVKCGGCFEAIAPNEFVMRAQKSVYHLSCFCCCVCERQLQKGDEFVLKEGQLLCKGDYEKERELLSLVSPAASDSGKSDDEESLCKSAHGAGKGTAEEGKDHKRPKRPRTILTTQQRRAFKASFEVSSKPCRKVRETLAAETGLSVRVVQVWFQNQRAKMKKLARRQQQQQQDQQNTQRLSSAQTNGGGSAGMEGIMNPYTALPTPQQLLAIEQSVYSSDPFRQGLTPPQMPGDHMHPYGAEPLFHDLDSDDTSLSNLGDCFLATSEAGPLQSRVGNPIDHLYSMQNSYFTS
" misc_feature 297..452 /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /note="The first LIM domain of Lmx1a; Region: LIM1_Lmx1a; cd09370" /db_xref="CDD:188756" misc_feature order(297..299,306..308,360..362,369..371,378..380, 387..389,438..440,447..449) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /note="Zn binding site [ion binding]; other site" /db_xref="CDD:188756" misc_feature 474..638 /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /note="The second LIM domain of Lmx1a and Lmx1b; Region: LIM2_Lmx1a_Lmx1b; cd09378" /db_xref="CDD:188764" misc_feature order(474..476,483..485,540..542,549..551,558..560, 567..569,624..626,633..635) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /note="Zn binding site [ion binding]; other site" /db_xref="CDD:188764" misc_feature 780..950 /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /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(780..794,798..800,849..851,867..869,906..908, 912..917,924..929,933..941,945..950) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /note="DNA binding site [nucleotide binding]" /db_xref="CDD:28970" misc_feature order(786..788,795..797,915..917,924..929,936..938) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /note="specific DNA base contacts [nucleotide binding]; other site" /db_xref="CDD:28970" variation complement(200) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:372269250" variation complement(203) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:144980188" variation complement(205) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="g" /db_xref="dbSNP:200643176" variation complement(227) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:377095215" variation complement(239) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="g" /db_xref="dbSNP:369951809" exon 271..457 /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /inference="alignment:Splign:1.39.8" variation complement(312) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="c" /db_xref="dbSNP:139738225" variation complement(313) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:199877582" variation complement(340) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:376967723" variation complement(365) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:144186336" variation complement(453) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="g" /db_xref="dbSNP:141657804" exon 458..690 /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /inference="alignment:Splign:1.39.8" variation complement(480) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:375082642" variation complement(489) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:202040732" variation complement(505) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:144319410" variation complement(533) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:35943978" variation complement(543) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:10753668" variation complement(545) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:370894937" variation complement(570) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:376042184" variation complement(574) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:150222420" variation complement(614) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="g" /replace="t" /db_xref="dbSNP:369819729" variation complement(638) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:145214876" variation complement(656) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:9970062" exon 691..863 /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /inference="alignment:Splign:1.39.8" variation complement(703) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:201194517" variation complement(719) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:141454506" variation complement(751..753) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="" /replace="ctg" /db_xref="dbSNP:376588006" variation complement(765) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:144871103" variation complement(774) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:149908681" variation complement(788) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:200303223" variation complement(833) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="c" /db_xref="dbSNP:34587265" variation complement(857) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:199831288" exon 864..941 /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /inference="alignment:Splign:1.39.8" variation complement(935) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:374849037" variation complement(938) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:146395249" exon 942..1011 /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /inference="alignment:Splign:1.39.8" variation complement(942) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="t" /db_xref="dbSNP:148303583" variation complement(957) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="t" /db_xref="dbSNP:367562812" variation complement(978..979) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="" /replace="agc" /db_xref="dbSNP:201457558" variation complement(979..980) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="" /replace="gca" /db_xref="dbSNP:144665555" variation complement(985) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:200350574" exon 1012..1182 /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /inference="alignment:Splign:1.39.8" variation complement(1041) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="t" /db_xref="dbSNP:146994534" variation complement(1043) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:373067545" variation complement(1051) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:202032483" variation complement(1066) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:370226701" variation complement(1067) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="g" /replace="t" /db_xref="dbSNP:200784612" variation complement(1077) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="c" /db_xref="dbSNP:148227502" variation complement(1080) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="c" /db_xref="dbSNP:140864022" variation complement(1092) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="c" /db_xref="dbSNP:377473482" variation complement(1098) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:150936773" variation complement(1125) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="g" /db_xref="dbSNP:186074862" variation complement(1145) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:35130714" variation complement(1151) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:374428255" variation complement(1170) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:369953981" variation complement(1175) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:116535186" variation complement(1179) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:200209751" exon 1183..3356 /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /inference="alignment:Splign:1.39.8" variation complement(1187) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:199560186" variation complement(1188) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:200583099" variation complement(1217) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:186807467" variation complement(1219) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:142270152" STS 1230..1720 /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /standard_name="LMX1A_7814" /db_xref="UniSTS:468079" variation complement(1244) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:1354509" variation complement(1246) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="g" /db_xref="dbSNP:148126113" variation complement(1254) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="" /replace="g" /db_xref="dbSNP:5778428" variation complement(1283) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:138842147" variation complement(1285) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:376073290" variation complement(1291) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:145918505" variation complement(1302) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="g" /replace="t" /db_xref="dbSNP:182575654" variation complement(1358) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:191246907" variation complement(1390) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:150977107" variation complement(1544) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:370020304" variation complement(1664) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:144312815" variation complement(1698) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:139580641" variation complement(1748..1749) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="" /replace="tg" /db_xref="dbSNP:150276008" variation complement(1764) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:41266638" variation complement(1922) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="t" /db_xref="dbSNP:74118516" variation complement(2024) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="t" /db_xref="dbSNP:143586869" variation complement(2029..2030) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="" /replace="ct" /db_xref="dbSNP:202181805" variation complement(2040) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:369994362" variation complement(2180) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:1936370" variation complement(2207) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:1936369" variation complement(2247) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:114236288" variation complement(2265) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="c" /db_xref="dbSNP:188596495" variation complement(2282) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:183552842" variation complement(2302) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="t" /db_xref="dbSNP:35479059" variation complement(2320..2321) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="" /replace="c" /db_xref="dbSNP:34736945" variation complement(2327) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="g" /db_xref="dbSNP:148808219" variation complement(2396) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="g" /db_xref="dbSNP:79244563" variation complement(2455) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="g" /replace="t" /db_xref="dbSNP:16840972" variation complement(2499) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:11579653" variation complement(2507) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="g" /db_xref="dbSNP:79493894" variation complement(2528) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:144378497" variation complement(2641) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:114160792" variation complement(2647) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="t" /db_xref="dbSNP:1553512" variation complement(2748) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:41266636" variation complement(2783) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:17402900" variation complement(2918) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:139366621" variation complement(2942) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:192272810" variation complement(2958) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:73027265" variation complement(2990) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="g" /replace="t" /db_xref="dbSNP:150866695" variation complement(3020) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:143525854" variation complement(3022) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:181899172" variation complement(3045) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="g" /replace="t" /db_xref="dbSNP:78693315" variation complement(3066) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:138006925" variation complement(3074) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:189523643" variation complement(3159) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:185154126" variation complement(3221) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="t" /db_xref="dbSNP:114221335" variation complement(3253) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="c" /replace="t" /db_xref="dbSNP:181151782" variation complement(3342) /gene="LMX1A" /gene_synonym="LMX1; LMX1.1" /replace="a" /replace="g" /db_xref="dbSNP:146940954" ORIGIN
ctcttttgcttctgcagacattcccggcactggccgactggcgggaggacctccccgcgcgccccgcacaccggctcctgcgcgcaccccaacagagcgcagcgccaggagtccagaagcgggcgggacgccctccgggtcccttacagtgccccttctcgacctggggcaggtcctcccggcccggcccgaacatgctggacggcctaaagatggaggagaacttccaaagcgcgatcgacacctcggcctccttctcctcgctgctgggcagagcggtgagccccaagtctgtctgcgagggctgtcagcgggtcatcttggacaggtttctgctgcggctcaacgacagcttctggcatgagcagtgcgtgcagtgcgcctcctgcaaagagcccctggagaccacctgcttctaccgggacaagaagctgtactgcaagtatgactacgagaagctgtttgctgttaaatgtgggggctgcttcgaggccatcgctcccaatgagtttgttatgcgggcccagaagagtgtataccacctgagctgcttctgctgctgtgtctgcgagcgacagcttcagaagggtgatgagtttgtcctgaaggaggggcagctgctctgcaaaggggactatgagaaggagcgggagctgctcagcctggtgagcccagcagcctcagactcaggtaaaagtgatgatgaagaaagtctctgcaagtcagcccatggggcagggaaaggaactgctgaggaaggcaaggaccataagcgccccaaacgtccgagaaccatcttgacaactcaacagaggcgagcattcaaggcctcatttgaagtatcctccaagccctgcaggaaggtgagagagactctggctgcagagacagggctgagtgtccgtgtcgtccaggtgtggttccaaaaccagagagcgaagatgaagaagctggccaggcgacagcagcagcagcagcaagatcagcagaacacccagaggctgagctctgctcagacaaacggtggtgggagtgctgggatggaaggaatcatgaacccctacacggctctgcccaccccacagcagctcctggccatcgagcagagtgtctacagctcagatcccttccgacagggtctcaccccaccccagatgcctggagaccacatgcacccttatggtgccgagccccttttccatgacctggatagcgacgacacctccctcagtaacctgggtgattgtttcctagcaacctcagaagctgggcctctgcagtccagagtgggaaaccccattgaccatctgtactccatgcagaattcttacttcacatcttgagtcttcccctagagttctgtgactaggctcccatatggaacaaccatattctttgaggggtcactggctttaggacagggaggccagggaagaggtgggttggggagggagttttgttggggatgctgttgtataatgatatggtgtagctcagcatttccaaagactgaatacattatggattgcatagtttaatgtttctaataagagtcttagcattagatatgaagacgtgtttatcattaaggacagagacttttaatatagacattctcatgcaaactagatacttagggactcctaacaacttcccaccatgtcggggaagctcttgtcaagaggtgcatatgtctatccatctacacaccaatagacagaaggacagatagatagatgtgtgtgtgtgagtgtgtaacctttcgtattttaccctcaaagtttattcctaattataacagacaccaactgtacagcaaaagtaactttattttcagtgtgaactatatttaaggaaatgcttgatgcacttaagttataaaatgagataatttacttttataaactttatttttagcttgacaagacttgtcagcagggcagagagggctgctccacctagccccatagctttgagtgctggggttcattctgttttcagagtgtctttcagatctggaaagaaattctgtgtggctgatggtgttctctcttgcattcttgctctctttggggttgaatcactgggcaggggtgggacagaataatctctgatcatgttctgagaaaatgtaaagcccagactcctgggctttcttttaaattctgacaagtggttgttgggcagtgctaggatgattggttcagctcttgagcttcagcatctgcaaatgtggatgaggctaatagtatgtacctacctcactgggaaacaccaaggcttaattcattcccaggacacatgagcagggctgagactaatatctgatatttgtttaagatacaaccaggccactcacttggcaaaggagggtacatagggttgcagagcaggagggctcctgaactccagagggcagttctgcctgctgaagtccctctgcaaagcctgtgctgaaggagacaccagctcagagcagttcagagggatcccagagtcccagagtggggaggaggtgaaggctgaggggatagaggagggcctggtggtgttctagagcagggttgggcaaactcctgcttgcgggcctgctttctatggcttgccagcaaagaatggtttttactttttttttgaggtcattaaaaaaaaggagaagaagaatatataacaggctgtctgtggcctggaaagcctgaaatatttgctatctgtattgtctggcccttacagaaaaagtttggggccccttgttttagagggtctgtttctaaagaacctcatggcgctcatagaggcagaaggttccagtggaaacccttggctcttccttccaactcactcctctgatcctcggcacagaagacccagcagccattgtacatggggacagttccacaccctggtctccagttgcggtgctaggatggtattgttctgtgctaggaagtctcctgggaacccagaatgagttggtggggaagacagcgggtcactgtggacccatccaggaggggccaggataggcttggcctcatttctggggacatcattggagacttgaacacagagacacgtccctatcactctggcaaggccagagggaacatgtccccttatggtagagtctatgttgtgtgatttttgtgctcttgtttataatttatgcaaaccaccaagaaacccaaaccagtctgatgagtgaaaattatgcagatgctgtatggccccacaggtttctgtggtaaagaccagttggagaatgtaggagatactatgtgagtgaaaatgaatagagatccttattccactccttaatggcataccaagatgaaattaaaatctcttacaaatgaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:4009 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: IEA GeneID:4009 -> Molecular function: GO:0008270 [zinc ion binding] evidence: IEA GeneID:4009 -> Molecular function: GO:0043565 [sequence-specific DNA binding] evidence: IEA GeneID:4009 -> Biological process: GO:0001558 [regulation of cell growth] evidence: IEA GeneID:4009 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IEA GeneID:4009 -> Biological process: GO:0007411 [axon guidance] evidence: IEA GeneID:4009 -> Biological process: GO:0021542 [dentate gyrus development] evidence: IEA GeneID:4009 -> Biological process: GO:0021549 [cerebellum development] evidence: IEA GeneID:4009 -> Biological process: GO:0021953 [central nervous system neuron differentiation] evidence: IEA GeneID:4009 -> Biological process: GO:0030901 [midbrain development] evidence: IEA GeneID:4009 -> Biological process: GO:0045665 [negative regulation of neuron differentiation] evidence: IEA GeneID:4009 -> Biological process: GO:0071542 [dopaminergic neuron differentiation] evidence: IEA GeneID:4009 -> Cellular component: GO:0005634 [nucleus] evidence: IEA
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