MYH14 - Gene browser

MYH14

myosin heavy chain 14

HCNC Approved Symbol: MYH14 (HGNC:23212)
Genomic Coordinates: 19:50,203,622 - 50,310,540 (19q13.33)
Synonyms: FLJ13881, KIAA2034, MHC16, MYH17, DFNA4
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

14Patients

In total, 14 patients were diagnosed with a variant in the MYH14 gene.

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

014
Patient count

Hearing loss: 6 (42.9%)
Patient Count: 6 (42.9%)
% of total patients presenting each phenotype is shown in parentheses.
6 (42.9%)
Distal limb muscle weakness: 1 (7.1%)
Patient Count: 1 (7.1%)
% of total patients presenting each phenotype is shown in parentheses.
1 (7.1%)
Foot drop: 1 (7.1%)
Patient Count: 1 (7.1%)
% of total patients presenting each phenotype is shown in parentheses.
1 (7.1%)
Lower limb muscle hypotrophy: 1 (7.1%)
Patient Count: 1 (7.1%)
% of total patients presenting each phenotype is shown in parentheses.
1 (7.1%)
Pain in extremities: 1 (7.1%)
Patient Count: 1 (7.1%)
% of total patients presenting each phenotype is shown in parentheses.
1 (7.1%)