Homo sapiens transient receptor potential cation channel subfamily M m - Nucleotide

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A Cataract-Causing Mutation in the TRPM3 Cation Channel Disrupts Calcium Dynamics in the Lens. [Cells. 2024]
A Cataract-Causing Mutation in the TRPM3 Cation Channel Disrupts Calcium Dynamics in the Lens.
Zhou Y, Bennett TM, Ruzycki PA, Guo Z, Cao YQ, Shahidullah M, Delamere NA, Shiels A. Cells. 2024 Jan 30; 13(3). Epub 2024 Jan 30.
TRPM3-Related Neurodevelopmental Disorder. [GeneReviews(®). 1993]
TRPM3-Related Neurodevelopmental Disorder.
Dyment D, Lines M, Innes AM. GeneReviews(®). 1993-2024. 2023 Feb 23
Role of novel de novo gain-of-function TRPM3 mutations in a spectrum of neurodevelopmental disorders. [Cell Calcium. 2023]
Role of novel de novo gain-of-function TRPM3 mutations in a spectrum of neurodevelopmental disorders.
Kashio M, Tominaga M. Cell Calcium. 2023 Mar; 110:102704. Epub 2023 Feb 13.

RefSeq alternative splicing
See 23 reference mRNA sequence splice variants for the TRPM3 gene.
RefSeq protein product
See the reference protein sequence for transient receptor potential cation channel subfamily M member 3 isoform m (NP_001353074.1).

Protein
Protein sequence from Nucleotide coding region
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Nucleotide