MYO7A - Gene browser

MYO7A

myosin VIIA

HCNC Approved Symbol: MYO7A (HGNC:7606)
Genomic Coordinates: 11:77,128,246 - 77,215,241 (11q13.5)
Synonyms: NSRD2, USH1B, DFNB2, DFNA11
Disease Associations: This gene is associated with the following 3 diseases in OMIM.

Diagnosed Cases

112Patients

In total, 112 patients were diagnosed with a variant in the MYO7A gene.

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

0112
Patient count

Hearing loss: 45 (40.2%)
Patient Count: 45 (40.2%)
% of total patients presenting each phenotype is shown in parentheses.
45 (40.2%)
Retinitis pigmentosa: 14 (12.5%)
Patient Count: 14 (12.5%)
% of total patients presenting each phenotype is shown in parentheses.
14 (12.5%)
Retinal dystrophy: 13 (11.6%)
Patient Count: 13 (11.6%)
% of total patients presenting each phenotype is shown in parentheses.
13 (11.6%)
Hearing impairment: 13 (11.6%)
Patient Count: 13 (11.6%)
% of total patients presenting each phenotype is shown in parentheses.
13 (11.6%)
Decreased visual acuity: 9 (8.0%)
Patient Count: 9 (8.0%)
% of total patients presenting each phenotype is shown in parentheses.
9 (8.0%)