The protein encoded by this gene is a member of the AAA family of adenosine triphosphatases (ATPases), is related to the Clp protease/heat shock family and is expressed prominently in the substantia nigra pars compacta. Mutations in this gene result in the autosomal dominant disorder, torsion dystonia 1.
A synthesized peptide derived from human Torc1/Crtc1, corresponding to a region within the internal amino acids.
A synthesized peptide derived from human TORC2, corresponding to a region within N-terminal amino acids.
A synthesized peptide derived from human TORC2.
A synthesized peptide derived from human TOX4.
A synthesized peptide derived from human TOX.
This gene is specifically expressed in the thymus, and encodes a protein that is localized to the mitochondrion. The expression of this gene is inducible by p53, and it is thought to play an important role in mediating p53-dependent apoptosis. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.
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