Gene entry
ALG8
ALG8 alpha-1,3-glucosyltransferase
- Chromosome
- 11
- Cytoband
- 11q14.1
- Variants (rsID)
- 14
ALG8 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11q14.1). Its official name is “ALG8 alpha-1,3-glucosyltransferase”. The reference table lists 14 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs17825668Benignsingle nucleotide variantALG8 congenital disorder of glycosylation
- rs61995925Benignsingle nucleotide variantALG8 congenital disorder of glycosylation
- rs139832787Conflicting interpretationssingle nucleotide variantALG8 congenital disorder of glycosylation
- rs199911532Conflicting interpretationssingle nucleotide variantALG8 congenital disorder of glycosylation
- rs200888240Pathogenicsingle nucleotide variantALG8 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.