Dehydrogenase E1 and transketolase domain containing 1 is a protein that in humans is encoded by the DHTKD1 gene. 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.^[5]

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DHTKD1
Identifiers
Aliases	DHTKD1, AMOXAD, CMT2Q, dehydrogenase E1 and transketolase domain containing 1, AAKAD
External IDs	OMIM: 614984; MGI: 2445096; HomoloGene: 10278; GeneCards: DHTKD1; OMA:DHTKD1 - orthologs
Gene location (Human) Chr. Chromosome 10 (human)[1] Band 10p14 Start 12,068,954 bp[1] End 12,123,221 bp[1]
Gene location (Mouse) Chr. Chromosome 2 (mouse)[2] Band 2|2 A1 Start 5,896,115 bp[2] End 5,942,792 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in liver right lobe of liver secondary oocyte parotid gland renal medulla ganglionic eminence kidney tubule kidney biceps brachii gastrocnemius muscle Top expressed in liver secondary oocyte left lobe of liver kidney spermatocyte proximal tubule parotid gland morula cumulus cell substantia nigra More reference expression data BioGPS n/a
Gene ontology Molecular function thiamine pyrophosphate binding oxidoreductase activity oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor oxoglutarate dehydrogenase (succinyl-transferring) activity Cellular component oxoglutarate dehydrogenase complex cytosol mitochondrial matrix mitochondrion Biological process metabolism tricarboxylic acid cycle glycolytic process generation of precursor metabolites and energy hematopoietic progenitor cell differentiation Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 55526 209692 Ensembl ENSG00000181192 ENSMUSG00000025815 UniProt Q96HY7 A2ATU0 RefSeq (mRNA) NM_018706 NM_001081131 RefSeq (protein) NP_061176 NP_001074600 Location (UCSC) Chr 10: 12.07 – 12.12 Mb Chr 2: 5.9 – 5.94 Mb PubMed search [3] [4]
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The DHTKD1 gene encodes a protein that has 919 amino acids, and is one of two isoforms within the 2-oxoglutarate-dehydrogenase complex.^[5]

DHTKD1 is part of an OGDHc-like supercomplex that is responsible for a crucial step in the degradation pathways of L-lysine, L-hydroxylysine, and L-tryptophan. Specifically, this enzyme catalyzes the decarboxylation of 2-oxoadipate to glutaryl-CoA.^[6] There is a strong correlation between DHTKD1 expression levels and ATP production, which signifies that DHTKD1 plays a critical role in energy production in mitochondria. Moreover, suppression of DHTKD1 results in decreased levels of biogenesis and increased levels of reactive oxygen species (ROS) within the mitochondria. Globally, this impairs cell growth and enhances cell apoptosis.^[7]

Mutations in the DHTKD1 gene are associated with alpha-aminoadipic and alpha-ketoadipic aciduria, an autosomal recessive inborn error of lysine, hydroxylysine, and tryptophan degradation. Only a handful of mutations have been observed in patients, including three missense mutations, two nonsense mutations, two splice donor mutations, one duplication, and one deletion and insertion. Two missense mutations are the most common cause of the deficiency. The clinical presentation of this disease in inconsistent.^[6][8]

Mutations in this gene could also cause neurological abnormalities.^[7] Indeed, one form of Charcot-Marie-Tooth (CMT) disease has been associated with DHTKD1, although the disease encompasses a wide spectrum of clinical neuropathies. Specifically, a hyterozygous nonsense mutation within the gene leads to decreased levels of DHTKD1 mRNA and proteins, and impaired ATP generation. This implicates this mutation as a causative agent for CMT-2 Disease.^[6]