Gene: TNNT3 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7140
Gene Symbol: TNNT3
TNNT3 		0.010 GeneticVariation disease BEFREE We establish a homozygous splice variant in TNNT3 as the likely cause of severe congenital NM with distal arthrogryposis, characterized by specific involvement of Type-2 fibers and deficiency of troponin-T<sub>fast</sub> . 29266598 2018