Identity
HGNC
LOCATION
9q21.12
LOCUSID
ALIAS
GON-2,LTRPC3,MLSN2
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 80036
MIM: 608961
HGNC: 17992
Ensembl: ENSG00000083067
Variants:
dbSNP: 80036
ClinVar: 80036
TCGA: ENSG00000083067
COSMIC: TRPM3
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38334649 | 2024 | A Cataract-Causing Mutation in the TRPM3 Cation Channel Disrupts Calcium Dynamics in the Lens. | 1 |
| 38917121 | 2024 | Novel characterization of endogenous transient receptor potential melastatin 3 ion channels from Gulf War Illness participants. | 0 |
| 38334649 | 2024 | A Cataract-Causing Mutation in the TRPM3 Cation Channel Disrupts Calcium Dynamics in the Lens. | 1 |
| 38917121 | 2024 | Novel characterization of endogenous transient receptor potential melastatin 3 ion channels from Gulf War Illness participants. | 0 |
| 36283409 | 2023 | Structural and functional analyses of a GPCR-inhibited ion channel TRPM3. | 13 |
| 36648066 | 2023 | Gain-of-function variants in the ion channel gene TRPM3 underlie a spectrum of neurodevelopmental disorders. | 8 |
| 36804759 | 2023 | Role of novel de novo gain-of-function TRPM3 mutations in a spectrum of neurodevelopmental disorders. | 0 |
| 36283409 | 2023 | Structural and functional analyses of a GPCR-inhibited ion channel TRPM3. | 13 |
| 36648066 | 2023 | Gain-of-function variants in the ion channel gene TRPM3 underlie a spectrum of neurodevelopmental disorders. | 8 |
| 36804759 | 2023 | Role of novel de novo gain-of-function TRPM3 mutations in a spectrum of neurodevelopmental disorders. | 0 |
| 34386996 | 2022 | A novel candidate gene in autosomal dominant facial pruritus. | 1 |
| 35146895 | 2022 | Phenotypic spectrum of the recurrent TRPM3 p.(Val837Met) substitution in seven individuals with global developmental delay and hypotonia. | 4 |
| 35240732 | 2022 | TRPM3 in the eye and in the nervous system - from new findings to novel mechanisms. | 3 |
| 36181791 | 2022 | Computational and functional studies of the PI(4,5)P(2) binding site of the TRPM3 ion channel reveal interactions with other regulators. | 3 |
| 34386996 | 2022 | A novel candidate gene in autosomal dominant facial pruritus. | 1 |
Citation
Dessen P
TRPM3 (transient receptor potential cation channel subfamily M member 3)
Atlas Genet Cytogenet Oncol Haematol. 2015-02-01
Online version: http://atlasgeneticsoncology.org/gene/55070/tumors-explorer/submit-meetings/
