Homo sapiens solute carrier family 4 member 3 (SLC4A3), RefSeqGene on - Nucleotide

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Genetic analysis identifies the SLC4A3 anion exchanger as a major gene for short QT syndrome. [Heart Rhythm. 2023]
Genetic analysis identifies the SLC4A3 anion exchanger as a major gene for short QT syndrome.
Christiansen MK, Kjær-Sørensen K, Clavsen NC, Dittmann S, Jensen MF, Guldbrandsen HØ, Pedersen LN, Sørensen RH, Lildballe DL, Müller K, et al. Heart Rhythm. 2023 Aug; 20(8):1136-1143. Epub 2023 Feb 15.
Chr21 protein-protein interactions: enrichment in proteins involved in intellectual disability, autism, and late-onset Alzheimer's disease. [Life Sci Alliance. 2022]
Chr21 protein-protein interactions: enrichment in proteins involved in intellectual disability, autism, and late-onset Alzheimer's disease.
Viard J, Loe-Mie Y, Daudin R, Khelfaoui M, Plancon C, Boland A, Tejedor F, Huganir RL, Kim E, Kinoshita M, et al. Life Sci Alliance. 2022 Aug 1; 5(12). Epub 2022 Aug 1.
RIG-I regulates myeloid differentiation by promoting TRIM25-mediated ISGylation. [Proc Natl Acad Sci U S A. 2020]
RIG-I regulates myeloid differentiation by promoting TRIM25-mediated ISGylation.
Wu SF, Xia L, Shi XD, Dai YJ, Zhang WN, Zhao JM, Zhang W, Weng XQ, Lu J, Le HY, et al. Proc Natl Acad Sci U S A. 2020 Jun 23; 117(25):14395-14404. Epub 2020 Jun 8.