Gene entry
FOXRED1
FAD dependent oxidoreductase domain containing 1
- Chromosome
- 11
- Cytoband
- 11q24.2
- Variants (rsID)
- 15
FOXRED1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11q24.2). Its official name is “FAD dependent oxidoreductase domain containing 1”. The reference table lists 15 variants (rsID) for this gene.
Clinically classified variants
13 reference-table entries with clinical significance.
- rs11220434Benignsingle nucleotide variant
- rs147235743Conflicting interpretationssingle nucleotide variantMitochondrial complex I deficiency, nuclear type 1
- rs148346044Conflicting interpretationssingle nucleotide variantMitochondrial complex I deficiency, nuclear type 1
- rs28372779Conflicting interpretationssingle nucleotide variantMitochondrial complex I deficiency, nuclear type 1
- rs34542988Conflicting interpretationssingle nucleotide variantMitochondrial complex I deficiency, nuclear type 1
- rs368307265Conflicting interpretationssingle nucleotide variantMitochondrial complex I deficiency, nuclear type 1
- rs398124308Conflicting interpretationsDuplicationMitochondrial complex I deficiency|Leigh syndrome|Mitochondrial complex I deficiency, nuclear type 1|Mitochondrial complex 1 deficiency, nuclear type 19
- rs7116126Conflicting interpretationssingle nucleotide variantMitochondrial complex I deficiency, nuclear type 1
- rs77785510Conflicting interpretationssingle nucleotide variantMitochondrial complex I deficiency, nuclear type 1
- rs267606830Pathogenicsingle nucleotide variantMitochondrial complex 1 deficiency, nuclear type 19
- rs373075574Pathogenicsingle nucleotide variantMitochondrial complex I deficiency|Mitochondrial complex 1 deficiency, nuclear type 19
- rs149883459Uncertain significancesingle nucleotide variantMitochondrial complex I deficiency, nuclear type 1
- rs191604046Uncertain significancesingle nucleotide variantMitochondrial complex I deficiency, nuclear type 1
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.