Homo sapiens ATP binding cassette subfamily A member 4 (ABCA4), RefSeq - Nucleotide

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Protein modeling and in silico analysis to assess pathogenicity of ABCA4 variants in patients with inherited retinal disease. [Mol Vis. 2023]
Protein modeling and in silico analysis to assess pathogenicity of ABCA4 variants in patients with inherited retinal disease.
Cevik S, Wangtiraumnuay N, Van Schelvergem K, Tsukikawa M, Capasso J, Biswas SB, Bodt B, Levin AV, Biswas-Fiss E. Mol Vis. 2023; 29:217-233. Epub 2023 Oct 25.
Major Contribution of c.[1622T>C;3113C>T] Complex Allele and c.5882G>A Variant in ABCA4-Related Retinal Dystrophy in an Eastern European Population. [Int J Mol Sci. 2023]
Major Contribution of c.[1622T>C;3113C>T] Complex Allele and c.5882G>A Variant in ABCA4-Related Retinal Dystrophy in an Eastern European Population.
Kadyshev VV, Alekseeva EA, Strelnikov VV, Stepanova AA, Polyakov AV, Marakhonov AV, Kutsev SI, Zinchenko RA. Int J Mol Sci. 2023 Nov 12; 24(22). Epub 2023 Nov 12.
Comprehensive genetic analysis reveals the mutational landscape of ABCA4-associated retinal dystrophy in a Chinese cohort. [Gene. 2024]
Comprehensive genetic analysis reveals the mutational landscape of ABCA4-associated retinal dystrophy in a Chinese cohort.
Tian L, Chen CJ, Song YN, Xu K, Li NE, Zhang XH, Xie Y, Jin ZB, Li Y. Gene. 2024 Jan 15; 891:147832. Epub 2023 Sep 27.

RefSeq alternative splicing
See 3 reference mRNA sequence splice variants for the ABCA4 gene.

Protein
Protein sequence from Nucleotide coding region
PubMed
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Taxonomy
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RNA
RNA sequence records that are annotated on the current genomic nucleotide sequences. The RNA records represent aligned or predicted transcripts of the current records.

Order Abca4 cDNA clone/Protein/Antibody/RNAi [OriGene]
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Nucleotide