Homo sapiens ATP binding cassette subfamily A member 2 (ABCA2), transc - Nucleotide

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Novel compound heterozygous ABCA2 variants cause IDPOGSA, a variable phenotypic syndrome with intellectual disability. [J Hum Genet. 2024]
Novel compound heterozygous ABCA2 variants cause IDPOGSA, a variable phenotypic syndrome with intellectual disability.
Inoue Y, Tsuchida N, Kim CA, de Oliveira Stephan B, Castro MAA, Honjo RS, Bertola DR, Uchiyama Y, Hamanaka K, Fujita A, et al. J Hum Genet. 2024 Apr; 69(3-4):163-167. Epub 2024 Jan 17.
A polymorphism in ABCA2 is associated with neutropenia induced by capecitabine in Japanese patients with colorectal cancer. [Cancer Chemother Pharmacol. 2023]
A polymorphism in ABCA2 is associated with neutropenia induced by capecitabine in Japanese patients with colorectal cancer.
Shibata Y, Matsumoto N, Murase R, Kubota Y, Ishida H, Shimada K, Fujita KI. Cancer Chemother Pharmacol. 2023 Dec; 92(6):465-474. Epub 2023 Aug 31.
Role of ABCA2 and its single nucleotide polymorphisms (4873T>A and 4879G>C) in the regulation of multi-drug resistance in oral squamous carcinoma cells. [Biochem Biophys Res Commun. 2023]
Role of ABCA2 and its single nucleotide polymorphisms (4873T>A and 4879G>C) in the regulation of multi-drug resistance in oral squamous carcinoma cells.
Kim MS, Yang SH, Kim MS. Biochem Biophys Res Commun. 2023 Jul 23; 666:1-9. Epub 2023 May 5.

RefSeq protein product
See the reference protein sequence for ATP-binding cassette sub-family A member 2 isoform b (NP_997698.1).

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Protein sequence from Nucleotide coding region
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Nucleotide