LDHD
Function
Involved in D-lactate, but not L-lactate catabolic process.
Involvement in disease
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.
Sequence Similarities
Belongs to the FAD-binding oxidoreductase/transferase type 4 family.
Tissue Specificity
Expressed moderately in heart and liver and at lower levels in skeletal muscle and kidney.
Cellular localization
- Mitochondrion
Alternative names
DLD, Lactate dehydrogenase D, LDHD