Gene entry
ALG11
ALG11 alpha-1,2-mannosyltransferase
- Chromosome
- 13
- Cytoband
- 13q14.3
- Variants (rsID)
- 4
ALG11 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 13 (region 13q14.3). Its official name is “ALG11 alpha-1,2-mannosyltransferase”. The reference table lists 4 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs146432805Benignsingle nucleotide variantALG11-congenital disorder of glycosylation
- rs2277448Benignsingle nucleotide variantCongenital disorder of glycosylation|Wilson disease
- rs77505745Likely benignsingle nucleotide variantALG11-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.