Involved in D-lactate, but not L-lactate catabolic process.
D-lactic aciduria with gout
DLACD
An autosomal recessive metabolic disorder characterized by D-lactic aciduria in the presence of normal plasma lactic acid.
None
The disease is caused by variants affecting the gene represented in this entry.
Belongs to the FAD-binding oxidoreductase/transferase type 4 family.
Expressed moderately in heart and liver and at lower levels in skeletal muscle and kidney.
DLD, Lactate dehydrogenase D, LDHD
Proteins
Metabolism
54871Da
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