Gene entry
PDHX
pyruvate dehydrogenase complex component X
- Chromosome
- 11
- Cytoband
- 11p13
- Variants (rsID)
- 27
PDHX is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11p13). Its official name is “pyruvate dehydrogenase complex component X”. The reference table lists 27 variants (rsID) for this gene.
Clinically classified variants
11 reference-table entries with clinical significance.
- rs113073242Benignsingle nucleotide variantPyruvate dehydrogenase E3-binding protein deficiency
- rs11539202Benignsingle nucleotide variantPyruvate dehydrogenase E3-binding protein deficiency
- rs148723565Benignsingle nucleotide variantPyruvate dehydrogenase E3-binding protein deficiency
- rs2767035Benignsingle nucleotide variantPyruvate dehydrogenase E3-binding protein deficiency
- rs2956114Benignsingle nucleotide variantPyruvate dehydrogenase E3-binding protein deficiency
- rs34398018Benignsingle nucleotide variantPyruvate dehydrogenase E3-binding protein deficiency
- rs61752925Benignsingle nucleotide variant
- rs139052284Conflicting interpretationssingle nucleotide variantPyruvate dehydrogenase E3-binding protein deficiency
- rs200438675Conflicting interpretationssingle nucleotide variantPyruvate dehydrogenase E3-binding protein deficiency
- rs35560997Conflicting interpretationssingle nucleotide variantPyruvate dehydrogenase E1-alpha deficiency|Pyruvate dehydrogenase E3-binding protein deficiency
- rs148645836Uncertain significancesingle nucleotide variantPyruvate dehydrogenase E3-binding protein 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.