Gene entry
DLAT
dihydrolipoamide S-acetyltransferase
- Chromosome
- 11
- Cytoband
- 11q23.1
- Variants (rsID)
- 11
DLAT is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11q23.1). Its official name is “dihydrolipoamide S-acetyltransferase”. The reference table lists 11 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs10891314Benignsingle nucleotide variantPyruvate dehydrogenase E2 deficiency
- rs2303436Benignsingle nucleotide variantPyruvate dehydrogenase E2 deficiency
- rs61757217Benignsingle nucleotide variantPyruvate dehydrogenase E2 deficiency
- rs77846695Benignsingle nucleotide variantPyruvate dehydrogenase E2 deficiency
- rs200500508Conflicting interpretationssingle nucleotide variantPyruvate dehydrogenase E2 deficiency
- rs199835215Likely benignsingle nucleotide variantPyruvate dehydrogenase E2 deficiency
- rs372355218Likely benignsingle nucleotide variantPyruvate dehydrogenase E2 deficiency
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.