MYF5 - Gene browser | 3billion

MYF5

MYF5

myogenic factor 5

HCNC Approved Symbol: MYF5 (HGNC:7565)
Genomic Coordinates: 12:80,716,912 - 80,719,671 (12q21.31)
Synonyms: bHLHc2
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

2Patients

In total, 2 patients were diagnosed with a variant in the MYF5 gene.

Frequently observed phenotypes(Top 5 only)

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

02
Patient count

Cfeom: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)
Congenital fibrosis of extraocular muscles: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)

Last updated: 2024-06-30

MYF5 - Gene browser | 3billion