ALG13 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human ALG13 wild-type allele is located in the vicinity of Xq23 and is approximately 95 kb in length. This allele, which encodes putative bifunctional UDP-N-acetylglucosamine transferase and deubiquitinase ALG13 protein, is involved in post-translational protein modification. Mutation of the gene is associated with developmental and epileptic encephalopathy 36.

**Synonyms:** - ALG13 UDP-N-Acetylglucosaminyltransferase Subunit wt Allele - ALG13, S. cerevisiae, Homolog of Gene - Asparagine-Linked Glycosylation 13 Homolog (S. cerevisiae) Gene - Asparagine-Linked Glycosylation 13 Homolog Gene - Asparagine-Linked Glycosylation 13, S. cerevisiae, Homolog of Gene - CDG1S - CXorf45 - Chromosome X Open Reading Frame 45 Gene - DEE36 - EIEE36 - FLJ23018 - GLT28D1 - Glycosyltransferase 28 Domain Containing 1 Gene - Glycosyltransferase 28 Domain-Containing 1 Gene - Hematopoietic Stem/Progenitor Cells Protein MDS031 Gene - MDS031 - N-Acetylglucosaminyldiphosphodolichol N-Acetylglucosaminyltransferase Gene - TDRD13 - Tudor Domain Containing 13 Gene - YGL047W