MYL3 - Gene browser

MYL3

myosin light chain 3

HCNC Approved Symbol: MYL3 (HGNC:7584)
Genomic Coordinates: 3:46,857,872 - 46,882,182 (3p21.31)
Synonyms: CMH8, VLC1, MLC1V, MLC1SB
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

52Patients

In total, 52 patients were diagnosed with a variant in the MYL3 gene.

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

052
Patient count

Left ventricular hypertrophy: 38 (73.1%)
Patient Count: 38 (73.1%)
% of total patients presenting each phenotype is shown in parentheses.
38 (73.1%)
Heart failure: 11 (21.2%)
Patient Count: 11 (21.2%)
% of total patients presenting each phenotype is shown in parentheses.
11 (21.2%)
Pain: 5 (9.6%)
Patient Count: 5 (9.6%)
% of total patients presenting each phenotype is shown in parentheses.
5 (9.6%)
Arrhythmias: 4 (7.7%)
Patient Count: 4 (7.7%)
% of total patients presenting each phenotype is shown in parentheses.
4 (7.7%)
Proteinuria: 3 (5.8%)
Patient Count: 3 (5.8%)
% of total patients presenting each phenotype is shown in parentheses.
3 (5.8%)