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Gene entry

MCEE

methylmalonyl-CoA epimerase

Chromosome
2
Cytoband
2p13.3
Variants (rsID)
7

MCEE is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2p13.3). Its official name is “methylmalonyl-CoA epimerase”. The reference table lists 7 variants (rsID) for this gene.

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Clinically classified variants

5 reference-table entries with clinical significance.

  • rs115175255Benignsingle nucleotide variantMethylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency
  • rs11541017Benignsingle nucleotide variantMethylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency
  • rs6748672Benignsingle nucleotide variantMethylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency
  • rs138436961Conflicting interpretationssingle nucleotide variantMethylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency
  • rs147401037Conflicting interpretationssingle nucleotide variantMethylmalonic acidemia due to methylmalonyl-CoA epimerase 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.