MYOZ2 - Gene browser | 3billion

MYOZ2

MYOZ2

myozenin 2

HCNC Approved Symbol: MYOZ2 (HGNC:1330)
Genomic Coordinates: 4:119,135,832 - 119,187,789 (4q26)
Synonyms: CS-1, FATZ-2, C4orf5
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the MYOZ2 gene.

Frequently observed phenotypes(Top 5 only)

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

01
Patient count

Hypertension: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Hypertensive retinopathy: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Left ventricular hypertrophy: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)

Last updated: 2024-06-30

MYOZ2 - Gene browser | 3billion