MYH7B - Gene browser

MYH7B

myosin heavy chain 7B

HCNC Approved Symbol: MYH7B (HGNC:15906)
Genomic Coordinates: 20:34,955,868 - 35,002,437 (20q11.22)
Synonyms: KIAA1512, dJ756N5.1, MYH14, MHC14, lncMYH7b
Disease Associations: Currently, this gene is not associated with any human disease in OMIM.
However, the following publication(s) suggest a possible gene disease association.

Diagnosed Cases

8Patients

In total, 8 patients were diagnosed with a variant in the MYH7B gene.

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

08
Patient count

Left ventricular hypertrophy: 8 (100.0%)
Patient Count: 8 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
8 (100.0%)
Hypertrophic cardiomyopathy: 1 (12.5%)
Patient Count: 1 (12.5%)
% of total patients presenting each phenotype is shown in parentheses.
1 (12.5%)
Palpitations: 1 (12.5%)
Patient Count: 1 (12.5%)
% of total patients presenting each phenotype is shown in parentheses.
1 (12.5%)
Presyncope: 1 (12.5%)
Patient Count: 1 (12.5%)
% of total patients presenting each phenotype is shown in parentheses.
1 (12.5%)
Right ventricular hypertrophy: 1 (12.5%)
Patient Count: 1 (12.5%)
% of total patients presenting each phenotype is shown in parentheses.
1 (12.5%)