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ALG9, alpha-1,2-mannosyltransferase
Symbols ALG9 ; CDG1L; DIBD1; LOH11CR1J
External IDs OMIM606941 MGI1924753 HomoloGene6756 GeneCards: ALG9 Gene
EC number,
RNA expression pattern
PBB GE ALG9 219374 s at tn.png
More reference expression data
Species Human Mouse
Entrez 79796 102580
Ensembl ENSG00000086848 ENSMUSG00000032059
UniProt Q9H6U8 Q8VDI9
RefSeq (mRNA) NM_001077690 NM_133981
RefSeq (protein) NP_001071158 NP_598742
Location (UCSC) Chr 11:
111.78 – 111.87 Mb
Chr 9:
50.78 – 50.84 Mb
PubMed search [1] [2]

Alpha-1,2-mannosyltransferase ALG9 is an enzyme that in humans is encoded by the ALG9 gene.[1][2][3]


  1. ^ Baysal BE, Willett-Brozick JE, Badner JA, Corona W, Ferrell RE, Nimgaonkar VL, Detera-Wadleigh SD (May 2002). "A mannosyltransferase gene at 11q23 is disrupted by a translocation breakpoint that co-segregates with bipolar affective disorder in a small family". Neurogenetics 4 (1): 43–53. doi:10.1007/s10048-001-0129-x. PMID 12030331. 
  2. ^ Frank CG, Grubenmann CE, Eyaid W, Berger EG, Aebi M, Hennet T (May 2004). "Identification and Functional Analysis of a Defect in the Human ALG9 Gene: Definition of Congenital Disorder of Glycosylation Type IL". Am J Hum Genet 75 (1): 146–50. doi:10.1086/422367. PMC 1181998. PMID 15148656. 
  3. ^ "Entrez Gene: ALG9 asparagine-linked glycosylation 9 homolog (S. cerevisiae, alpha- 1,2-mannosyltransferase)". 

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