STRC - Gene browser | 3billion

STRC

STRC

stereocilin

HCNC Approved Symbol: STRC (HGNC:16035)
Genomic Coordinates: 15:43,599,563 - 43,618,800 (15q15.3)
Synonyms: DFNB16
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

28Patients

In total, 28 patients were diagnosed with a variant in the STRC gene.

Frequently observed phenotypes(Top 5 only)

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

028
Patient count

Hearing loss: 9 (32.1%)
Patient Count: 9 (32.1%)
% of total patients presenting each phenotype is shown in parentheses.
9 (32.1%)
Mild hearing impairment: 2 (7.1%)
Patient Count: 2 (7.1%)
% of total patients presenting each phenotype is shown in parentheses.
2 (7.1%)
Hearing impairment: 1 (3.6%)
Patient Count: 1 (3.6%)
% of total patients presenting each phenotype is shown in parentheses.
1 (3.6%)

Last updated: 2024-06-30

STRC - Gene browser | 3billion