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Protein Coding Gene : Alg9 ALG9 alpha-1,2-mannosyltransferase
Primary Identifier  MGI:1924753 Organism  mouse, laboratory
Chromosome  9 NCBI Gene Number  102580
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Predicted to enable dol-P-Man:Man(6)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase activity and dol-P-Man:Man(8)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase activity. Predicted to be involved in dolichol-linked oligosaccharide biosynthetic process. Predicted to be active in endoplasmic reticulum membrane. Is expressed in cortical plate. Human ortholog(s) of this gene implicated in congenital disorder of glycosylation Il. Orthologous to human ALG9 (ALG9 alpha-1,2-mannosyltransferase).
  • synonyms:
  • disrupted in bipolar disorder 1 homolog (human),
  • AI747665,
  • expressed sequence AI747665,
  • RIKEN cDNA B430313H07 gene,
  • MGI:2143117,
  • B430313H07Rik,
  • MGI:1925236,
  • ALG9 alpha-1,2-mannosyltransferase,
  • Alg9,
  • 8230402H15Rik,
  • RIKEN cDNA 8230402H15 gene,
  • Dibd1
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