TRPM4
From SNPedia
| is a | gene |
| is | mentioned by |
| Full name | transient receptor potential cation channel subfamily M member 4 |
| EntrezGene | 54795 |
| PheGenI | 54795 |
| VariationViewer | 54795 |
| ClinVar | TRPM4 |
| GeneCards | TRPM4 |
| dbSNP | 54795 |
| Diseases | TRPM4 |
| SADR | 54795 |
| HugeNav | 54795 |
| wikipedia | TRPM4 |
| TRPM4 | |
| gopubmed | TRPM4 |
| EVS | TRPM4 |
| HEFalMp | TRPM4 |
| MyGene2 | TRPM4 |
| 23andMe | TRPM4 |
| UniProt | Q8TD43 |
| Ensembl | ENSG00000130529 |
| OMIM | 606936 |
| # SNPs | 7 |
| Max Magnitude | Chromosome position | Summary | |
|---|---|---|---|
| rs172149856 | 5 | 49,188,641 | |
| rs172151858 | 7 | 49,200,395 | |
| rs200038418 | 7 | 49,196,760 | |
| rs201907325 | 7 | 49,182,608 | |
| rs267607142 | 7 | 49,157,885 | |
| rs387907216 | 7 | 49,168,301 | |
| rs71352737 | 0 | 49,182,889 |
The TRPM4 gene on chromosome 19 encodes the transient receptor potential cation channel subfamily M member 4 (hTRPM4), also known as melastatin-4.Wikipedia
Heterozygous (and therefore dominantly inherited) gain-of-function mutations in the TRPM4 gene have been linked to Progressive familial heart block type 1B (typically considered a form of Brugada syndrome).
