Gene entry
MN1
MN1 proto-oncogene, transcriptional regulator
- Chromosome
- 22
- Cytoband
- 22q12.1
- Variants (rsID)
- 26
MN1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 22 (region 22q12.1). Its official name is “MN1 proto-oncogene, transcriptional regulator”. The reference table lists 26 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs147334255Conflicting interpretationssingle nucleotide variantInborn genetic diseases|CEBALID syndrome|MN1 C-terminal truncation (MCTT) syndrome
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.