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TRPM4 - transient receptor potential cation channel subfamily M member 4
- Synonym(s) : FLJ20041
- Previous symbols and names : transient receptor potential cation channel, subfamily M, member 4
- Type : gene with protein product
- Chromosomal location : 19q13.33
- OMIM: 606936
- HGNC: 17993
- UniProtKB: Q8TD43
- Genatlas: TRPM4
- GenCC: TRPM4
- Ensembl: ENSG00000130529
- IUPHAR-DB: 496
- Reactome: Q8TD43
- LOVD: TRPM4
Diseases list
- Disease-causing germline mutation(s) (gain of function) in Familial progressive cardiac conduction defect
ORPHA:871 
- Disease-causing germline mutation(s) (gain of function) in Progressive symmetric erythrokeratodermia
ORPHA:316 - Candidate gene tested in Brugada syndrome
ORPHA:130
: AssessedAdditional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
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