TNNT3 - Gene browser

TNNT3

troponin T3, fast skeletal type

HCNC Approved Symbol: TNNT3 (HGNC:11950)
Genomic Coordinates: 11:1,919,552 - 1,938,702 (11p15.5)
Synonyms: AMCD2B, DA2B, FSSV, DKFZp779M2348
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

1Patient

In total, 1 patient was diagnosed with a variant in the TNNT3 gene.

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

01
Patient count

Arthrogryposis multiplex congenita: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Bilateral talipes equinovarus: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Distal arthrogryposis: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Interphalangeal joint contracture of finger: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Interphalangeal joint flexion contractures: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)