Gene entry
ACAD9
acyl-CoA dehydrogenase family member 9
- Chromosome
- 3
- Cytoband
- 3q21.3
- Variants (rsID)
- 16
ACAD9 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3q21.3). Its official name is “acyl-CoA dehydrogenase family member 9”. The reference table lists 16 variants (rsID) for this gene.
Clinically classified variants
11 reference-table entries with clinical significance.
- rs138871762Benignsingle nucleotide variantAcyl-CoA dehydrogenase 9 deficiency
- rs16852179Benignsingle nucleotide variant
- rs4494951Benignsingle nucleotide variantAcyl-CoA dehydrogenase 9 deficiency
- rs79530903Benignsingle nucleotide variantAcyl-CoA dehydrogenase 9 deficiency
- rs9830739Benignsingle nucleotide variantAcyl-CoA dehydrogenase 9 deficiency
- rs139145143Conflicting interpretationssingle nucleotide variantAcyl-CoA dehydrogenase 9 deficiency
- rs149753643Pathogenicsingle nucleotide variantAcyl-CoA dehydrogenase 9 deficiency|Mitochondrial complex I deficiency
- rs150283105Pathogenicsingle nucleotide variantAcyl-CoA dehydrogenase 9 deficiency|Mitochondrial complex I deficiency
- rs368949613Pathogenicsingle nucleotide variantAcyl-CoA dehydrogenase 9 deficiency
- rs377022708Pathogenicsingle nucleotide variantAcyl-CoA dehydrogenase 9 deficiency|Mitochondrial complex I deficiency
- rs370266841Uncertain significancesingle nucleotide variantAcyl-CoA dehydrogenase 9 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.