Gene entry
DPM1
dolichyl-phosphate mannosyltransferase subunit 1, catalytic
- Chromosome
- 20
- Cytoband
- 20q13.13
- Variants (rsID)
- 7
DPM1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 20 (region 20q13.13). Its official name is “dolichyl-phosphate mannosyltransferase subunit 1, catalytic”. The reference table lists 7 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs16995639Benignsingle nucleotide variantCongenital disorder of glycosylation type 1E
- rs139624629Conflicting interpretationssingle nucleotide variantCongenital disorder of glycosylation type 1E
- rs201392536Conflicting interpretationssingle nucleotide variantCongenital disorder of glycosylation type 1E
- rs779869066Conflicting interpretationssingle nucleotide variantCongenital disorder of glycosylation type 1E
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.