RecName: Full=Solute carrier family 22 member 12; AltName: Full=Organi - Protein

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New SLC22A12 (URAT1) Variant Associated with Renal Hypouricemia Identified by Whole-Exome Sequencing Analysis and Bioinformatics Predictions. [Genes (Basel). 2023]
New SLC22A12 (URAT1) Variant Associated with Renal Hypouricemia Identified by Whole-Exome Sequencing Analysis and Bioinformatics Predictions.
Perdomo-Ramírez A, Ramos-Trujillo E, Claverie-Martín F, RenalTube Group. Genes (Basel). 2023 Sep 20; 14(9). Epub 2023 Sep 20.
The impact of an URAT1 polymorphism on the losartan treatment of hypertension and hyperuricemia. [J Clin Lab Anal. 2021]
The impact of an URAT1 polymorphism on the losartan treatment of hypertension and hyperuricemia.
Wu L, Fan Y, Wang Y, Li Z, Mao D, Zhuang W. J Clin Lab Anal. 2021 Oct; 35(10):e23949. Epub 2021 Sep 8.
Genetic epidemiological analysis of hypouricaemia from 4993 Japanese on non-functional variants of URAT1/SLC22A12 gene. [Rheumatology (Oxford). 2022]
Genetic epidemiological analysis of hypouricaemia from 4993 Japanese on non-functional variants of URAT1/SLC22A12 gene.
Nakayama A, Kawamura Y, Toyoda Y, Shimizu S, Kawaguchi M, Aoki Y, Takeuchi K, Okada R, Kubo Y, Imakiire T, et al. Rheumatology (Oxford). 2022 Mar 2; 61(3):1276-1281.

RefSeq protein isoforms
See 8 reference sequence protein isoforms for the SLC22A12 gene.

PubMed
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Q96S37 [Domain Mapping of Disease Mut...]
Q96S37
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
Reactome [Reactome]
Reactome
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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Protein