Gene entry
RMND1
required for meiotic nuclear division 1 homolog
- Chromosome
- 6
- Cytoband
- 6q25.1
- Variants (rsID)
- 9
RMND1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6q25.1). Its official name is “required for meiotic nuclear division 1 homolog”. The reference table lists 9 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs142588921Conflicting interpretationssingle nucleotide variantCombined oxidative phosphorylation defect type 11
- rs144972972Conflicting interpretationssingle nucleotide variantMitochondrial disease|Combined oxidative phosphorylation defect type 11|Mitochondrial oxidative phosphorylation disorder|Nephronophthisis
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.