Gene entry
ALG9
ALG9 alpha-1,2-mannosyltransferase
- Chromosome
- 11
- Cytoband
- 11q23.1
- Variants (rsID)
- 14
ALG9 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11q23.1). Its official name is “ALG9 alpha-1,2-mannosyltransferase”. The reference table lists 14 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs12575909Benignsingle nucleotide variantALG9 congenital disorder of glycosylation
- rs36111204Conflicting interpretationssingle nucleotide variantGillessen-Kaesbach-Nishimura syndrome|ALG9 congenital disorder of glycosylation|Autosomal dominant polycystic liver disease|ALG9 congenital disorder of glycosylation|See cases
- rs121908023Pathogenicsingle nucleotide variantALG9 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.