ALG12 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human ALG12 wild-type allele is located in the vicinity of 22q13.33 and is approximately 59 kb in length. This allele, which encodes Dol-P-Man:Man(7)GlcNAc(2)-PP-Dol alpha-1,6-mannosyltransferase protein, is involved in the synthesis of complex oligosaccharides used in N-linked glycoproteins. Mutation of the gene is associated with congenital disorder of glycosylation type 1g.

**Synonyms:** - ALG12 Alpha-1,6-Mannosyltransferase wt Allele - ALG12, S. cerevisiae, Homolog of Gene - Asparagine-Linked Glycosylation 12 Homolog (S. cerevisiae, Alpha-1,6-Mannosyltransferase) Gene - Asparagine-Linked Glycosylation 12 Homolog (Yeast, Alpha-1,6-Mannosyltransferase) Gene - Asparagine-Linked Glycosylation 12, Alpha-1,6-Mannosyltransferase Homolog (S. cerevisiae) Gene - Asparagine-Linked Glycosylation 12, Alpha-1,6-Mannosyltransferase Homolog Gene - Asparagine-Linked Glycosylation 12, Homolog of Gene - CDG1G - ECM39 - PP14673 - hALG12