Homo sapiens ATP-binding cassette sub-family A member 2 (ABCA2) mRNA, - 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 alternative splicing
See 5 reference mRNA sequence splice variants for the ABCA2 gene.

C-type lectin domain family 14 member A [Loxodonta africana]
C-type lectin domain family 14 member A [Loxodonta africana]
gi|2710891799|ref|XP_003408510.2|

Protein
Homo sapiens general transcription factor IIIC, polypeptide 1, alpha 220kDa (GTF...
Homo sapiens general transcription factor IIIC, polypeptide 1, alpha 220kDa (GTF3C1), mRNA
gi|4753160|ref|NM_001520.1|

Nucleotide
trnA(ugc) [Diopatra cuprea]
trnA(ugc) [Diopatra cuprea]
Gene ID:68625160

Gene
0007-4640[ISSN] (1)
NLM Catalog
Puccinia oxalidis (1)
Taxonomy

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Nucleotide