Gene entry
ALG2
ALG2 alpha-1,3/1,6-mannosyltransferase
- Chromosome
- 9
- Cytoband
- 9q22.33
- Variants (rsID)
- 4
ALG2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9q22.33). Its official name is “ALG2 alpha-1,3/1,6-mannosyltransferase”. The reference table lists 4 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs180849348Benignsingle nucleotide variantALG2-congenital disorder of glycosylation|Congenital myasthenic syndrome 14
- rs62562374Benignsingle nucleotide variantALG2-congenital disorder of glycosylation|Congenital myasthenic syndrome 14
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.