Homo sapiens solute carrier family 37 member 4 (SLC37A4), transcript v - Nucleotide

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Treatment recommendations for glycogen storage disease type IB- associated neutropenia and neutrophil dysfunction with empagliflozin: Consensus from an international workshop. [Mol Genet Metab. 2024]
Treatment recommendations for glycogen storage disease type IB- associated neutropenia and neutrophil dysfunction with empagliflozin: Consensus from an international workshop.
Grünert SC, Derks TGJ, Mundy H, Dalton RN, Donadieu J, Hofbauer P, Jones N, Uçar SK, LaFreniere J, Contreras EL, et al. Mol Genet Metab. 2024 Mar; 141(3):108144. Epub 2024 Jan 17.
Multisite phosphorylation dictates selective E2-E3 pairing as revealed by Ubc8/UBE2H-GID/CTLH assemblies. [Mol Cell. 2024]
Multisite phosphorylation dictates selective E2-E3 pairing as revealed by Ubc8/UBE2H-GID/CTLH assemblies.
Chrustowicz J, Sherpa D, Li J, Langlois CR, Papadopoulou EC, Vu DT, Hehl LA, Karayel Ö, Beier V, von Gronau S, et al. Mol Cell. 2024 Jan 18; 84(2):293-308.e14. Epub 2023 Dec 18.
Three novel SLC37A4 variants in glycogen storage disease type 1b and a literature review. [J Int Med Res. 2023]
Three novel SLC37A4 variants in glycogen storage disease type 1b and a literature review.
Wang Z, Zhao R, Jia X, Li X, Ma L, Fu H. J Int Med Res. 2023 Dec; 51(12):3000605231216633.

RefSeq alternative splicing
See 5 reference mRNA sequence splice variants for the SLC37A4 gene.
RefSeq protein product
See the reference protein sequence for glucose-6-phosphate exchanger SLC37A4 isoform 1 (NP_001157749.1).

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Nucleotide