Homo sapiens cDNA FLJ43063 fis, clone BRTHA3008310, moderately similar - Nucleotide

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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.

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Nucleotide