TRPC6 - Gene browser

TRPC6

transient receptor potential cation channel subfamily C member 6

HCNC Approved Symbol: TRPC6 (HGNC:12338)
Genomic Coordinates: 11:101,451,564 - 101,584,007 (11q22.1)
Synonyms: TRP6, FSGS2
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

8Patients

In total, 8 patients were diagnosed with a variant in the TRPC6 gene.

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

08
Patient count

Nephrotic syndrome: 4 (50.0%)
Patient Count: 4 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
4 (50.0%)
Proteinuria: 3 (37.5%)
Patient Count: 3 (37.5%)
% of total patients presenting each phenotype is shown in parentheses.
3 (37.5%)
Focal segmental glomerulosclerosis: 3 (37.5%)
Patient Count: 3 (37.5%)
% of total patients presenting each phenotype is shown in parentheses.
3 (37.5%)
Nephrotic syndrome, steroid-resistant: 2 (25.0%)
Patient Count: 2 (25.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (25.0%)
Steroid-resistant nephrotic syndrome: 2 (25.0%)
Patient Count: 2 (25.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (25.0%)