Homo sapiens ATP binding cassette subfamily C member 8 (ABCC8), transc - Nucleotide

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Congenital Hyperinsulinism Caused by Mutations in ABCC8 Gene Associated with Early-Onset Neonatal Hypoglycemia: Genetic Heterogeneity Correlated with Phenotypic Variability. [Int J Mol Sci. 2024]
Congenital Hyperinsulinism Caused by Mutations in ABCC8 Gene Associated with Early-Onset Neonatal Hypoglycemia: Genetic Heterogeneity Correlated with Phenotypic Variability.
Butnariu LI, Bizim DA, Păduraru G, Păduraru L, Moisă ȘM, Popa S, Gimiga N, Ghiga G, Bădescu MC, Lupu A, et al. Int J Mol Sci. 2024 May 19; 25(10). Epub 2024 May 19.
Dynamic duo: Kir6 and SUR in K(ATP) channel structure and function. [Channels (Austin). 2024]
Dynamic duo: Kir6 and SUR in K(ATP) channel structure and function.
Patton BL, Zhu P, ElSheikh A, Driggers CM, Shyng SL. Channels (Austin). 2024 Dec; 18(1):2327708. Epub 2024 Mar 15.
An analysis of the relationship between ABCC8 and KCNJ11 gene polymorphisms and diabetic retinopathy in Turkish population. [Ophthalmic Genet. 2024]
An analysis of the relationship between ABCC8 and KCNJ11 gene polymorphisms and diabetic retinopathy in Turkish population.
Alp E, Doguizi S, Mutlu Icduygu F, Akgun E, Sekeroglu MA, Ozer MA. Ophthalmic Genet. 2024 Apr; 45(2):126-132. Epub 2024 Feb 27.

RefSeq protein product
See the reference protein sequence for ATP-binding cassette sub-family C member 8 isoform 5 (NP_001338226.1).

Protein
Protein sequence from Nucleotide coding region
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Homo sapiens ATP binding cassette subfamily C member 8 (ABCC8), transcript varia...
Homo sapiens ATP binding cassette subfamily C member 8 (ABCC8), transcript variant 5, mRNA
gi|1677501940|ref|NM_001351297.2|

Nucleotide

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Nucleotide