rs375541349
This variant is located in the DHTKD1 gene.
▶ClinVar annotation
About DHTKD1
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]
View all DHTKD1 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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