Official Full Name
DnaJ (Hsp40) homolog, subfamily C, member 19
The protein encoded by this gene is thought to be part of a complex involved in the ATP-dependent transport of transit peptide-containing proteins from the inner cell membrane to the mitochondrial matrix. Defects in this gene are a cause of 3-methylglutaconic aciduria type 5 (MGA5), also known as dilated cardiomyopathy with ataxia (DCMA). Several transcript variants, some protein-coding and some not, have been found for this gene.
DNAJC19; DnaJ (Hsp40) homolog, subfamily C, member 19; mitochondrial import inner membrane translocase subunit TIM14; Pam18; Tim14; TIMM14; DnaJ homolog subfamily C member 19; homolog of yeast TIM14; TIM 14; TIMM 14; translocase of the inner mitochondrial membrane 14; FLJ99060; zgc:73251