MYO6 - Gene browser

MYO6

myosin VI

HCNC Approved Symbol: MYO6 (HGNC:7605)
Genomic Coordinates: 6:75,749,239 - 75,919,537 (6q14.1)
Synonyms: KIAA0389, DFNA22, DFNB37
Disease Associations: This gene is associated with the following 3 diseases in OMIM.

Diagnosed Cases

21Patients

In total, 21 patients were diagnosed with a variant in the MYO6 gene.

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

021
Patient count

Hearing loss: 9 (42.9%)
Patient Count: 9 (42.9%)
% of total patients presenting each phenotype is shown in parentheses.
9 (42.9%)
Hearing impairment: 2 (9.5%)
Patient Count: 2 (9.5%)
% of total patients presenting each phenotype is shown in parentheses.
2 (9.5%)
Congenital deafness: 2 (9.5%)
Patient Count: 2 (9.5%)
% of total patients presenting each phenotype is shown in parentheses.
2 (9.5%)
Developmental delay: 2 (9.5%)
Patient Count: 2 (9.5%)
% of total patients presenting each phenotype is shown in parentheses.
2 (9.5%)
High frequency hearing loss: 1 (4.8%)
Patient Count: 1 (4.8%)
% of total patients presenting each phenotype is shown in parentheses.
1 (4.8%)