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Gene entry

ACAD8

acyl-CoA dehydrogenase family member 8

Chromosome
11
Cytoband
11q25
Variants (rsID)
13

ACAD8 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11q25). Its official name is “acyl-CoA dehydrogenase family member 8”. The reference table lists 13 variants (rsID) for this gene.

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Clinically classified variants

7 reference-table entries with clinical significance.

  • rs121908419Conflicting interpretationssingle nucleotide variantDeficiency of isobutyryl-CoA dehydrogenase
  • rs121908420Conflicting interpretationssingle nucleotide variantDeficiency of isobutyryl-CoA dehydrogenase
  • rs374317179Conflicting interpretationssingle nucleotide variantDeficiency of isobutyryl-CoA dehydrogenase
  • rs121908418Uncertain significancesingle nucleotide variantDeficiency of isobutyryl-CoA dehydrogenase
  • rs121908422Uncertain significancesingle nucleotide variantDeficiency of isobutyryl-CoA dehydrogenase
  • rs186756646Uncertain significancesingle nucleotide variantDeficiency of isobutyryl-CoA dehydrogenase
  • rs751633406Uncertain significancesingle nucleotide variantDeficiency of isobutyryl-CoA dehydrogenase

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.