Homo sapiens retina and anterior neural fold homeobox 2 (RAX2), transc - Nucleotide

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Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease. [Genet Med. 2019]
Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease.
Van de Sompele S, Smith C, Karali M, Corton M, Van Schil K, Peelman F, Cherry T, Rosseel T, Verdin H, Derolez J, et al. Genet Med. 2019 Jun; 21(6):1319-1329. Epub 2018 Oct 31.
TreeGrafter: phylogenetic tree-based annotation of proteins with Gene Ontology terms and other annotations. [Bioinformatics. 2019]
TreeGrafter: phylogenetic tree-based annotation of proteins with Gene Ontology terms and other annotations.
Tang H, Finn RD, Thomas PD. Bioinformatics. 2019 Feb 1; 35(3):518-520.
Autosomal Dominant Retinal Dystrophy With Electronegative Waveform Associated With a Novel RAX2 Mutation. [JAMA Ophthalmol. 2015]
Autosomal Dominant Retinal Dystrophy With Electronegative Waveform Associated With a Novel RAX2 Mutation.
Yang P, Chiang PW, Weleber RG, Pennesi ME. JAMA Ophthalmol. 2015 Jun; 133(6):653-61.

RefSeq alternative splicing
See the other reference mRNA sequence splice variant for the RAX2 gene (NM_001319074.4).
RefSeq protein product
See the reference protein sequence for retina and anterior neural fold homeobox protein 2 (NP_116142.1).

Protein
Protein sequence from Nucleotide coding region
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GenScript latest version of gene cDNA ORF Clone [GenScript latest version of g...]
GenScript latest version of gene cDNA ORF Clone
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Homo sapiens retina and anterior neural fold homeobox 2 (RAX2), transcript varia...
Homo sapiens retina and anterior neural fold homeobox 2 (RAX2), transcript variant 2, mRNA
gi|1677530400|ref|NM_032753.4|

Nucleotide

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Nucleotide