Gene entry
ALG14
ALG14 UDP-N-acetylglucosaminyltransferase subunit
- Chromosome
- 1
- Cytoband
- 1p21.3
- Variants (rsID)
- 14
ALG14 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p21.3). Its official name is “ALG14 UDP-N-acetylglucosaminyltransferase subunit”. The reference table lists 14 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs199689080Uncertain significancesingle nucleotide variantCongenital myasthenic syndrome 15|Myopathy, epilepsy, and progressive cerebral atrophy
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.