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DHTKD1 - dehydrogenase E1 and transketolase domain containing 1

This gene encodes a component of a mitochondrial 2-oxoglutarate-dehydrogenase-complex-like protein involved in the degradation pathways of several amino acids, including lysine. Mutations in this gene are associated with 2-aminoadipic 2-oxoadipic aciduria and Charcot-Marie-Tooth Disease Type 2Q. [provided by RefSeq, May 2013]

Genes similar to DHTKD1

NCBI Orthologs

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Species Gene Architecture aa