Symbol
| TRPM1
| contributors: mct/shn - updated : 14-06-2016
|
HGNC name
| transient receptor potential cation channel, subfamily M, member 1
|
HGNC id
| 7146
|
corresponding disease(s)
|
CSNB1C
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
tumoral
|  
|  
| --low
|  
|
in melanoma with high metastatic potential | |
Variant & Polymorphism
|
| |
Candidate gene
Marker
Therapy target
| potential target for pigmentation disorders |
| | |
| decreased expression of TRPM1 in the eye and the skin may alter bipolar cell signaling as well as melanocyte function, thus causing both congenital stationary night blindness and coat spotting patterns in horses | |
ON bipolar cell function was absent or severely impaired in a mouse model that lacked Trpm1 expression |