TRPM1 - Gene browser

TRPM1

transient receptor potential cation channel subfamily M member 1

HCNC Approved Symbol: TRPM1 (HGNC:7146)
Genomic Coordinates: 15:31,001,065 - 31,161,160 (15q13.3)
Synonyms: LTRPC1, CSNB1C, MLSN1
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

13Patients

In total, 13 patients were diagnosed with a variant in the TRPM1 gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

013
Patient count

Congenital stationary night blindness: 11 (84.6%)
Patient Count: 11 (84.6%)
% of total patients presenting each phenotype is shown in parentheses.
11 (84.6%)
Night blindness: 2 (15.4%)
Patient Count: 2 (15.4%)
% of total patients presenting each phenotype is shown in parentheses.
2 (15.4%)
Abnormality of vision: 2 (15.4%)
Patient Count: 2 (15.4%)
% of total patients presenting each phenotype is shown in parentheses.
2 (15.4%)
Vision issue: 2 (15.4%)
Patient Count: 2 (15.4%)
% of total patients presenting each phenotype is shown in parentheses.
2 (15.4%)
Retinitis pigmentosa: 1 (7.7%)
Patient Count: 1 (7.7%)
% of total patients presenting each phenotype is shown in parentheses.
1 (7.7%)