Gene entry
MGAT2
alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase
- Chromosome
- 14
- Cytoband
- 14q21.3
- Variants (rsID)
- 4
MGAT2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 14 (region 14q21.3). Its official name is “alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase”. The reference table lists 4 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs148802016Benignsingle nucleotide variantMGAT2-congenital disorder of glycosylation
- rs9989177Benignsingle nucleotide variantPrimary ciliary dyskinesia|Congenital disorder of glycosylation|Primary ciliary dyskinesia 10
- rs140584714Conflicting interpretationssingle nucleotide variantMGAT2-congenital disorder of glycosylation
- rs146729850Conflicting interpretationssingle nucleotide variantMGAT2-congenital disorder of glycosylation
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.