DNAJC19, DnaJ heat shock protein family (Hsp40) member C19

DNAJC19, DnaJ heat shock protein family (Hsp40) member C19

• 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). Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 1, 2, 6, 10, 14 and 19. [provided by RefSeq, Jan 2012]

• Gene Synonyms (PAM18, TIM14, TIMM14, mitochondrial import inner membrane translocase subunit TIM14, DnaJ (Hsp40) homolog, subfamily C, member 19, DnaJ-like protein subfamily C member 19, homolog of yeast TIM14,)
• NCBI Gene ID: 131118
• Species: Homo sapiens (Human)
• UNIPROT ID#>>A0A0S2Z5X1
  UNIPROT ID#>>Q96DA6
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

DnaJ heat shock protein family (Hsp40) member C19 interacts with:

• major facilitator superfamily domain containing 8
  solute carrier family 2 member 12
  solute carrier family 39 member 12

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.