Gene entry
MOCS1
molybdenum cofactor synthesis 1
- Chromosome
- 6
- Cytoband
- 6p21.2
- Variants (rsID)
- 24
MOCS1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6p21.2). Its official name is “molybdenum cofactor synthesis 1”. The reference table lists 24 variants (rsID) for this gene.
Clinically classified variants
11 reference-table entries with clinical significance.
- rs11968529Benignsingle nucleotide variantSulfite oxidase deficiency due to molybdenum cofactor deficiency type A
- rs35825585Benignsingle nucleotide variantSulfite oxidase deficiency due to molybdenum cofactor deficiency type A
- rs41273140Benignsingle nucleotide variantSulfite oxidase deficiency due to molybdenum cofactor deficiency type A
- rs41273142Benignsingle nucleotide variantSulfite oxidase deficiency due to molybdenum cofactor deficiency type A
- rs7762875Benignsingle nucleotide variantSulfite oxidase deficiency due to molybdenum cofactor deficiency type A
- rs140243105Conflicting interpretationssingle nucleotide variantSulfite oxidase deficiency due to molybdenum cofactor deficiency type A|Intellectual disability
- rs104893970Likely pathogenicsingle nucleotide variantSulfite oxidase deficiency due to molybdenum cofactor deficiency type A
- rs104893969Pathogenicsingle nucleotide variantSulfite oxidase deficiency due to molybdenum cofactor deficiency type A
- rs142478972Uncertain significancesingle nucleotide variantSulfite oxidase deficiency due to molybdenum cofactor deficiency type A
- rs143912353Uncertain significancesingle nucleotide variantSulfite oxidase deficiency due to molybdenum cofactor deficiency type A
- rs144238782Uncertain significancesingle nucleotide variantSulfite oxidase deficiency due to molybdenum cofactor deficiency type A
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.