Gene entry
MPI
mannose phosphate isomerase
- Chromosome
- 15
- Cytoband
- 15q24.1-q24.2
- Variants (rsID)
- 11
MPI is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 15 (region 15q24.1-q24.2). Its official name is “mannose phosphate isomerase”. The reference table lists 11 variants (rsID) for this gene.
Clinically classified variants
8 reference-table entries with clinical significance.
- rs116933453Benignsingle nucleotide variantMPI-congenital disorder of glycosylation
- rs117089191Benignsingle nucleotide variantMPI-congenital disorder of glycosylation
- rs7495739Benignsingle nucleotide variantMPI-congenital disorder of glycosylation
- rs139228075Conflicting interpretationssingle nucleotide variantMPI-congenital disorder of glycosylation
- rs143982014Conflicting interpretationssingle nucleotide variantMPI-congenital disorder of glycosylation
- rs104894489Pathogenicsingle nucleotide variantMPI-congenital disorder of glycosylation
- rs28928906Pathogenicsingle nucleotide variantMPI-congenital disorder of glycosylation
- rs201815588Uncertain significancesingle nucleotide variantMPI-congenital disorder of glycosylation
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.