TPM1 - Gene browser

TPM1

tropomyosin 1

HCNC Approved Symbol: TPM1 (HGNC:12010)
Genomic Coordinates: 15:63,042,747 - 63,071,915 (15q22.2)
Synonyms: C15orf13, CMH3
Disease Associations: This gene is associated with the following 3 diseases in OMIM.

53Patients

In total, 53 patients were diagnosed with a variant in the TPM1 gene.

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

053
Patient count

Left ventricular hypertrophy: 42 (79.2%)
Patient Count: 42 (79.2%)
% of total patients presenting each phenotype is shown in parentheses.
42 (79.2%)
Pain: 8 (15.1%)
Patient Count: 8 (15.1%)
% of total patients presenting each phenotype is shown in parentheses.
8 (15.1%)
Arrhythmias: 7 (13.2%)
Patient Count: 7 (13.2%)
% of total patients presenting each phenotype is shown in parentheses.
7 (13.2%)
Hypertrophic cardiomyopathy: 5 (9.4%)
Patient Count: 5 (9.4%)
% of total patients presenting each phenotype is shown in parentheses.
5 (9.4%)
Heart failure: 5 (9.4%)
Patient Count: 5 (9.4%)
% of total patients presenting each phenotype is shown in parentheses.
5 (9.4%)