MYO3A - Gene browser | 3billion

MYO3A

MYO3A

myosin IIIA

HCNC Approved Symbol: MYO3A (HGNC:7601)
Genomic Coordinates: 10:25,934,229 - 26,212,532 (10p12.1)
Synonyms: DFNB30
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

5Patients

In total, 5 patients were diagnosed with a variant in the MYO3A gene.

Frequently observed phenotypes(Top 5 only)

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

05
Patient count

Hearing loss: 5 (100.0%)
Patient Count: 5 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
5 (100.0%)
Retinal dystrophy: 1 (20.0%)
Patient Count: 1 (20.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (20.0%)

Last updated: 2024-06-30

MYO3A - Gene browser | 3billion