2025-05-09 19:15:45, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_024336 2308 bp mRNA linear PRI 17-APR-2013 DEFINITION Homo sapiens iroquois homeobox 3 (IRX3), mRNA. ACCESSION NM_024336 XM_113857 VERSION NM_024336.2 GI:226371734 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 2308) AUTHORS Murea,M., Lu,L., Ma,L., Hicks,P.J., Divers,J., McDonough,C.W., Langefeld,C.D., Bowden,D.W. and Freedman,B.I. TITLE Genome-wide association scan for survival on dialysis in African-Americans with type 2 diabetes JOURNAL Am. J. Nephrol. 33 (6), 502-509 (2011) PUBMED 21546767 REFERENCE 2 (bases 1 to 2308) AUTHORS Ragvin,A., Moro,E., Fredman,D., Navratilova,P., Drivenes,O., Engstrom,P.G., Alonso,M.E., de la Calle Mustienes,E., Gomez Skarmeta,J.L., Tavares,M.J., Casares,F., Manzanares,M., van Heyningen,V., Molven,A., Njolstad,P.R., Argenton,F., Lenhard,B. and Becker,T.S. TITLE Long-range gene regulation links genomic type 2 diabetes and obesity risk regions to HHEX, SOX4, and IRX3 JOURNAL Proc. Natl. Acad. Sci. U.S.A. 107 (2), 775-780 (2010) PUBMED 20080751 REMARK GeneRIF: IRX3 function may have a direct functional relationship to both obesity and type 2 diabetes. Erratum:[Proc Natl Acad Sci U S A. 2011 Mar 8;108(10):4264] REFERENCE 3 (bases 1 to 2308) AUTHORS Trynka,G., Zhernakova,A., Romanos,J., Franke,L., Hunt,K.A., Turner,G., Bruinenberg,M., Heap,G.A., Platteel,M., Ryan,A.W., de Kovel,C., Holmes,G.K., Howdle,P.D., Walters,J.R., Sanders,D.S., Mulder,C.J., Mearin,M.L., Verbeek,W.H., Trimble,V., Stevens,F.M., Kelleher,D., Barisani,D., Bardella,M.T., McManus,R., van Heel,D.A. and Wijmenga,C. TITLE Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-kappaB signalling JOURNAL Gut 58 (8), 1078-1083 (2009) PUBMED 19240061 REMARK GeneRIF: Observational study of gene-disease association. (HuGE Navigator) REFERENCE 4 (bases 1 to 2308) AUTHORS Lewis,M.T., Ross,S., Strickland,P.A., Snyder,C.J. and Daniel,C.W. TITLE Regulated expression patterns of IRX-2, an Iroquois-class homeobox gene, in the human breast JOURNAL Cell Tissue Res. 296 (3), 549-554 (1999) PUBMED 10370142 REFERENCE 5 (bases 1 to 2308) AUTHORS Bellefroid,E.J., Kobbe,A., Gruss,P., Pieler,T., Gurdon,J.B. and Papalopulu,N. TITLE Xiro3 encodes a Xenopus homolog of the Drosophila Iroquois genes and functions in neural specification JOURNAL EMBO J. 17 (1), 191-203 (1998) PUBMED 9427753 COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AY335943.1 and BC023667.2. On Apr 4, 2009 this sequence version replaced gi:39930458. Summary: IRX3 is a member of the Iroquois homeobox gene family (see IRX1; MIM 606197) and plays a role in an early step of neural development (Bellefroid et al., 1998 [PubMed 9427753]). Members of this family appear to play multiple roles during pattern formation of vertebrate embryos (Lewis et al., 1999 [PubMed 10370142]).[supplied by OMIM, Aug 2009]. ##Evidence-Data-START## Transcript exon combination :: AY335943.1, BC023667.2 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025083, ERS025085 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-1079 AY335943.1 1-1079 1080-1680 BC023667.2 1047-1647 1681-2308 AY335943.1 1681-2308 FEATURES Location/Qualifiers source 1..2308 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="16" /map="16q12.2" gene 1..2308 /gene="IRX3" /gene_synonym="IRX-1; IRXB1" /note="iroquois homeobox 3" /db_xref="GeneID:79191" /db_xref="HGNC:14360" /db_xref="MIM:612985" exon 1..683 /gene="IRX3" /gene_synonym="IRX-1; IRXB1" /inference="alignment:Splign:1.39.8" misc_feature 15..17 /gene="IRX3" /gene_synonym="IRX-1; IRXB1" /note="upstream in-frame stop codon" variation 182 /gene="IRX3" /gene_synonym="IRX-1; IRXB1" /replace="a" /replace="c" /db_xref="dbSNP:3751723" variation 245..256 /gene="IRX3" /gene_synonym="IRX-1; IRXB1" /replace="" /replace="cgtcgccgccgc" /db_xref="dbSNP:3833834" variation 385 /gene="IRX3" /gene_synonym="IRX-1; IRXB1" /replace="c" /replace="g" /db_xref="dbSNP:1868691" CDS 417..1922 /gene="IRX3" /gene_synonym="IRX-1; IRXB1" /note="iroquois homeobox protein 3; iroquois-class homeodomain protein IRX-1; homeodomain protein IRXB1" /codon_start=1 /product="iroquois-class homeodomain protein IRX-3" /protein_id="NP_077312.2" /db_xref="GI:226371735" /db_xref="CCDS:CCDS10750.1" /db_xref="GeneID:79191" /db_xref="HGNC:14360" /db_xref="MIM:612985" /translation="
MSFPQLGYQYIRPLYPSERPGAAGGSGGSAGARGGLGAGASELNASGSLSNVLSSVYGAPYAAAAAAAAAQGYGAFLPYAAELPIFPQLGAQYELKDSPGVQHPAAAAAFPHPHPAFYPYGQYQFGDPSRPKNATRESTSTLKAWLNEHRKNPYPTKGEKIMLAIITKMTLTQVSTWFANARRRLKKENKMTWAPRSRTDEEGNAYGSEREEEDEEEDEEDGKRELELEEEELGGEEEDTGGEGLADDDEDEEIDLENLDGAATEPELSLAGAARRDGDLGLGPISDSKNSDSEDSSEGLEDRPLPVLSLAPAPPPVAVASPSLPSPPVSLDPCAPAPAPASALQKPKIWSLAETATSPDNPRRSPPGAGGSPPGAAVAPSALQLSPAAAAAAAHRLVSAPLGKFPAWTNRPFPGPPPGPRLHPLSLLGSAPPHLLGLPGAAGHPAAAAAFARPAEPEGGTDRCSALEVEKKLLKTAFQPVPRRPQNHLDAALVLSALSSS
" misc_feature 819..983 /gene="IRX3" /gene_synonym="IRX-1; IRXB1" /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(876..878,894..896,933..935,939..944,951..956, 960..968,972..977) /gene="IRX3" /gene_synonym="IRX-1; IRXB1" /note="DNA binding site [nucleotide binding]" /db_xref="CDD:28970" misc_feature order(942..944,951..956,963..965) /gene="IRX3" /gene_synonym="IRX-1; IRXB1" /note="specific DNA base contacts [nucleotide binding]; other site" /db_xref="CDD:28970" misc_feature 1446..1493 /gene="IRX3" /gene_synonym="IRX-1; IRXB1" /note="Motif in Iroquois-class homeodomain proteins (only). Unknown function; Region: IRO; smart00548" /db_xref="CDD:128821" exon 684..1800 /gene="IRX3" /gene_synonym="IRX-1; IRXB1" /inference="alignment:Splign:1.39.8" STS 854..918 /gene="IRX3" /gene_synonym="IRX-1; IRXB1" /standard_name="Irx3" /db_xref="UniSTS:498475" STS 966..1045 /gene="IRX3" /gene_synonym="IRX-1; IRXB1" /standard_name="Irx3" /db_xref="UniSTS:532300" variation 1681 /gene="IRX3" /gene_synonym="IRX-1; IRXB1" /replace="c" /replace="t" /db_xref="dbSNP:1450355" exon 1801..1867 /gene="IRX3" /gene_synonym="IRX-1; IRXB1" /inference="alignment:Splign:1.39.8" variation 1853 /gene="IRX3" /gene_synonym="IRX-1; IRXB1" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1126960" exon 1868..2308 /gene="IRX3" /gene_synonym="IRX-1; IRXB1" /inference="alignment:Splign:1.39.8" STS 2032..2186 /gene="IRX3" /gene_synonym="IRX-1; IRXB1" /standard_name="SHGC-61146" /db_xref="UniSTS:59616" variation 2111 /gene="IRX3" /gene_synonym="IRX-1; IRXB1" /replace="c" /replace="t" /db_xref="dbSNP:1042899" variation 2261 /gene="IRX3" /gene_synonym="IRX-1; IRXB1" /replace="a" /replace="c" /db_xref="dbSNP:2278810" ORIGIN
gcgaggagggggagtgaaaactagaggagggcgaaggaagcgaggcgcgacactgctggggagaggagggcagtgaggagcgaggagcgggcagaggcagctccggcggccgagaggagggagcgcggcgcagagaggaggggcttgcgccccgtagaaatgtcaatcagagcccggagccccgggaatctccgccaatctgttcggacctgacctggctcctcgccgccgccctcgccgccgccgtcgccgccgcggagcagatcaataggcgaacgcggagcacagcgcagcgcgggcggcagcgcggccccaagcccggcccagcccccgatgcgcgccggagcccgcgggcggcgctgagctgggcggcccgggggtcggcccccctctccgtccgtgccccgcgggccaccatgtccttcccccagctgggataccaatacatccgcccgctttacccgtccgagcgcccgggggccgctggcggcagcggcggcagcgcgggggcccggggcggcctgggtgccggagcctcggagctgaacgcctcggggtccctgtccaacgtgctctcgtccgtgtacggggcgccctacgccgcggccgctgcggccgccgccgcccaaggctacggcgccttcctgccctacgccgcggagctgcccatcttcccgcagctgggcgcgcagtatgagctgaaggacagccccggggtgcagcatccggccgcggctgccgcgtttccgcacccgcaccccgccttctacccgtatggccagtaccagttcggggacccgtcccgtcccaagaacgccaccagggagagcaccagcacgctgaaggcctggctcaacgagcaccgcaagaacccctaccccaccaagggcgagaagatcatgctggccatcatcaccaagatgaccctcacccaggtgtccacctggttcgccaacgcgcgccggcgcctcaagaaggagaataagatgacttgggcgcctcgcagccgcactgacgaggagggaaacgcttatgggagcgagcgcgaggaggaagacgaagaggaggacgaggaggacggcaaacgcgagctagagctggaggaggaggagctcgggggggaggaggaggacacggggggcgagggcctggctgacgacgacgaggacgaggagatcgatttggagaacttagacggcgcggccaccgagcctgagctgtccctggctggggcggcgcgcagggatggcgacctaggcctgggacccatttcggactccaaaaatagcgactcggaagatagctctgagggcttagaggaccggccactaccggtcctgagtctggctccagcgccaccaccagtggccgtggcctcgccgtctctgccgtcgccccccgtgagcctggacccctgcgctcccgcaccagcccccgcctccgccctgcagaagcccaagatctggtccctcgcggagactgccacaagcccggacaacccgcgccgctcgcctcccggcgcgggggggtctccaccgggggcagcggtcgcgccttccgccctgcagctctctccggccgccgccgccgccgccgctcacagactggtctcagcgccgctgggcaagttcccggcttggaccaaccggccgtttccaggcccaccgcccggcccccgcctgcacccgctctccctgctgggctctgcccctccgcacctgctgggacttcccggagccgcgggccacccggctgccgccgccgccttcgctcggccagcggagcccgaaggcggaacagatcgctgtagtgccttggaagtggagaaaaagttactcaagacagctttccagcccgtgcccaggcggccccagaaccatctggacgccgccctggtcttatcggctctctcctcatcctagttctttaaaaaaaacaaaaaaacaaaaaaaactttttttaatcgttgtaataattgtataaaaaaaatcgctctgtatagttacaacttgtaagcatgtccgtgtataaatacctaaaagcaaaactaaacaaagaaagtaagaaaaagaaataaaaccagtcctcctcagccctccccaagtcgcttctgtggcaccccgcattcgctgtgaggtttgtttgtccggttgattttggggggtggagtttcagtgagaataaacgtgtctgcctttgtgtgtgtgtatatatacagagaaatgtacatatgtgtgaaccaaattgtacgagaaagtatctatttttggctaaataaatgagctgctgccactttgactataacccg
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ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:79191 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: IEA GeneID:79191 -> Molecular function: GO:0043565 [sequence-specific DNA binding] evidence: IEA GeneID:79191 -> Biological process: GO:0001656 [metanephros development] evidence: IEA GeneID:79191 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IEA GeneID:79191 -> Biological process: GO:0007498 [mesoderm development] evidence: IEA GeneID:79191 -> Biological process: GO:0045665 [negative regulation of neuron differentiation] evidence: IEA GeneID:79191 -> Biological process: GO:0045666 [positive regulation of neuron differentiation] evidence: IEA GeneID:79191 -> Biological process: GO:0072086 [specification of loop of Henle identity] evidence: IEA GeneID:79191 -> Cellular component: GO:0005634 [nucleus] evidence: IEA GeneID:79191 -> Cellular component: GO:0005737 [cytoplasm] evidence: IEA GeneID:79191 -> Cellular component: GO:0030424 [axon] evidence: IEA
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