Homo sapiens facilitative glucose transporter family member GLUT9 (SLC - Nucleotide

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Raised CK and acute kidney injury following intense exercise in three patients with a history of exercise intolerance due to homozygous mutations in SLC2A9. [Neuromuscul Disord. 2024]
Raised CK and acute kidney injury following intense exercise in three patients with a history of exercise intolerance due to homozygous mutations in SLC2A9.
Quinlivan R, Murphy E, Pula S, Pain A, Brain H, Scopes G, Gjika F, Ahmadouk N, Manole A, Houlden H. Neuromuscul Disord. 2024 Jan; 34:49-53. Epub 2023 Dec 6.
GLUT9 as a potential drug target for chronic kidney disease: Drug target validation by a Mendelian randomization study. [J Hum Genet. 2023]
GLUT9 as a potential drug target for chronic kidney disease: Drug target validation by a Mendelian randomization study.
Ueda M, Fukui K, Kamatani N, Kamitsuji S, Matsuo A, Sasase T, Nishiu J, Matsushita M. J Hum Genet. 2023 Oct; 68(10):699-704. Epub 2023 Jun 13.
Pathogenic Variants of SLC22A12 (URAT1) and SLC2A9 (GLUT9) in Spanish Patients with Renal Hypouricemia: Founder Effect of SLC2A9 Variant c.374C>T; p.(T125M). [Int J Mol Sci. 2023]
Pathogenic Variants of SLC22A12 (URAT1) and SLC2A9 (GLUT9) in Spanish Patients with Renal Hypouricemia: Founder Effect of SLC2A9 Variant c.374C>T; p.(T125M).
Perdomo-Ramirez A, Cordoba-Lanus E, Trujillo-Frias CJ, Gonzalez-Navasa C, Ramos-Trujillo E, Luis-Yanes MI, Garcia-Nieto V, Claverie-Martin F, RenalTube. Int J Mol Sci. 2023 May 8; 24(9). Epub 2023 May 8.

RefSeq alternative splicing
See 53 reference mRNA sequence splice variants for the SLC2A9 gene.

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myosin regulatory light polypeptide 9 isoform a [Homo sapiens]
myosin regulatory light polypeptide 9 isoform a [Homo sapiens]
gi|29568111|ref|NP_006088.2|

Protein

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Nucleotide