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Gene entry

ACADM

acyl-CoA dehydrogenase medium chain

Chromosome
1
Cytoband
1p31.1
Variants (rsID)
32

ACADM is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p31.1). Its official name is “acyl-CoA dehydrogenase medium chain”. The reference table lists 32 variants (rsID) for this gene.

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Clinically classified variants

27 reference-table entries with clinical significance.

  • rs1061337Benignsingle nucleotide variantMedium-chain acyl-coenzyme A dehydrogenase deficiency
  • rs143911981Benignsingle nucleotide variantMedium-chain acyl-coenzyme A dehydrogenase deficiency
  • rs2229249Benignsingle nucleotide variantMedium-chain acyl-coenzyme A dehydrogenase deficiency
  • rs74090726Benignsingle nucleotide variantMCAD deficiency, modifier of|Medium-chain acyl-coenzyme A dehydrogenase deficiency
  • rs121434283Conflicting interpretationssingle nucleotide variantMedium-chain acyl-coenzyme A dehydrogenase deficiency
  • rs138098371Conflicting interpretationssingle nucleotide variantMedium-chain acyl-coenzyme A dehydrogenase deficiency
  • rs147559466Conflicting interpretationssingle nucleotide variantMedium-chain acyl-coenzyme A dehydrogenase deficiency|See cases
  • rs149678400Conflicting interpretationssingle nucleotide variantMedium-chain acyl-coenzyme A dehydrogenase deficiency
  • rs200754053Conflicting interpretationssingle nucleotide variantMedium-chain acyl-coenzyme A dehydrogenase deficiency
  • rs201375579Conflicting interpretationssingle nucleotide variantMedium-chain acyl-coenzyme A dehydrogenase deficiency|Epileptic spasm
  • rs745844469Conflicting interpretationssingle nucleotide variantMedium-chain acyl-coenzyme A dehydrogenase deficiency
  • rs747268471Conflicting interpretationssingle nucleotide variantMedium-chain acyl-coenzyme A dehydrogenase deficiency
  • rs754359356Conflicting interpretationssingle nucleotide variantMedium-chain acyl-coenzyme A dehydrogenase deficiency
  • rs77931234Conflicting interpretationssingle nucleotide variantMedium-chain acyl-coenzyme A dehydrogenase deficiency|Epileptic spasm|Abnormal circulating lipid concentration|Medium chain dicarboxylic aciduria|See cases
  • rs121434274Pathogenicsingle nucleotide variantMedium-chain acyl-coenzyme A dehydrogenase deficiency
  • rs121434277Pathogenicsingle nucleotide variantMedium-chain acyl-coenzyme A dehydrogenase deficiency
  • rs121434278Pathogenicsingle nucleotide variantMedium-chain acyl-coenzyme A dehydrogenase deficiency
  • rs121434280Pathogenicsingle nucleotide variantMedium-chain acyl-coenzyme A dehydrogenase deficiency
  • rs121434281Pathogenicsingle nucleotide variantMedium-chain acyl-coenzyme A dehydrogenase deficiency
  • rs148207467Pathogenicsingle nucleotide variantMedium-chain acyl-coenzyme A dehydrogenase deficiency
  • rs200724875Pathogenicsingle nucleotide variantMedium-chain acyl-coenzyme A dehydrogenase deficiency
  • rs373715782Pathogenicsingle nucleotide variantMedium-chain acyl-coenzyme A dehydrogenase deficiency
  • rs762114560Pathogenicsingle nucleotide variantMedium-chain acyl-coenzyme A dehydrogenase deficiency
  • rs779759347Pathogenicsingle nucleotide variantMedium-chain acyl-coenzyme A dehydrogenase deficiency
  • rs786204566PathogenicDuplicationMedium-chain acyl-coenzyme A dehydrogenase deficiency
  • rs866388216Pathogenicsingle nucleotide variantMedium-chain acyl-coenzyme A dehydrogenase deficiency
  • rs875989875PathogenicDuplicationMedium-chain acyl-coenzyme A dehydrogenase 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.