Homo sapiens iroquois homeobox 6 (IRX6), mRNA

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A duplication on chromosome 16q12 affecting the IRXB gene cluster is associated with autosomal dominant cone dystrophy with early tritanopic color vision defect. [Hum Mol Genet. 2021]
A duplication on chromosome 16q12 affecting the IRXB gene cluster is associated with autosomal dominant cone dystrophy with early tritanopic color vision defect.
Kohl S, Llavona P, Sauer A, Reuter P, Weisschuh N, Kempf M, Dehmelt FA, Arrenberg AB, Sliesoraityte I, Zrenner E, et al. Hum Mol Genet. 2021 Jun 17; 30(13):1218-1229.
A reference map of the human binary protein interactome. [Nature. 2020]
A reference map of the human binary protein interactome.
Luck K, Kim DK, Lambourne L, Spirohn K, Begg BE, Bian W, Brignall R, Cafarelli T, Campos-Laborie FJ, Charloteaux B, et al. Nature. 2020 Apr; 580(7803):402-408. Epub 2020 Apr 8.
Single Nucleotide Polymorphisms of HAAO and IRX6 Genes as Risk Factors for Hypospadias. [J Urol. 2019]
Single Nucleotide Polymorphisms of HAAO and IRX6 Genes as Risk Factors for Hypospadias.
Kojima Y, Koguchi T, Mizuno K, Sato Y, Hoshi S, Hata J, Nishio H, Hashimoto D, Matsushita S, Suzuki K, et al. J Urol. 2019 Feb; 201(2):386-392.

RefSeq alternative splicing
See 3 reference mRNA sequence splice variants for the IRX6 gene.
RefSeq protein product
See the reference protein sequence for iroquois-class homeodomain protein IRX-6 (NP_077311.2).

Protein
Protein sequence from Nucleotide coding region
PubMed
PubMed articles cited by Nucleotide sequence record
Taxonomy
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Annotated Genomic
Genomic sequence records that have the current RNA records as annotated features marking the exons of genes.
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Functional Class
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OMIM
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PubMed (RefSeq)
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PubMed (Weighted)
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GenScript latest version of gene cDNA ORF Clone [GenScript latest version of g...]
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Nucleotide