transient receptor potential cation channel, subfamily M, member 1, is - Protein

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Clinical and genetic findings in TRPM1-related congenital stationary night blindness. [Acta Ophthalmol. 2022]
Clinical and genetic findings in TRPM1-related congenital stationary night blindness.
Iosifidis C, Liu J, Gale T, Ellingford JM, Campbell C, Ingram S, Chandler K, Parry NRA, Black GC, Sergouniotis PI. Acta Ophthalmol. 2022 Sep; 100(6):e1332-e1339. Epub 2022 May 28.
Association Analysis Between Common Variants of the TRPM1 Gene and Three Mental Disorders in the Han Chinese Population. [Genet Test Mol Biomarkers. 2020]
Association Analysis Between Common Variants of the TRPM1 Gene and Three Mental Disorders in the Han Chinese Population.
Ma C, Li X, Chen J, Li Z, Guan J, Li Y, Yin S, Shi Y. Genet Test Mol Biomarkers. 2020 Oct; 24(10):649-657. Epub 2020 Oct 1.
A case of melanoma-associated retinopathy with autoantibodies against TRPM1. [Doc Ophthalmol. 2020]
A case of melanoma-associated retinopathy with autoantibodies against TRPM1.
Kim MS, Hong HK, Ko YJ, Park KH, Ueno S, Okado S, Woo SJ, Joo K. Doc Ophthalmol. 2020 Dec; 141(3):313-318. Epub 2020 May 29.

RefSeq genomic sequence
See the genomic reference sequence for the TRPM1 gene (NG_016453.2).
RefSeq protein isoforms
See 10 reference sequence protein isoforms for the TRPM1 gene.