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).