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Gene : ALG8 Homo sapiens

Name  ? ALG8 alpha-1,3-glucosyltransferase Cytological Location  11q14.1
Brief Description  ALG8, alpha-1,3-glucosyltransferase
description  This gene encodes a member of the ALG6/ALG8 glucosyltransferase family. The encoded protein catalyzes the addition of the second glucose residue to the lipid-linked oligosaccharide precursor for N-linked glycosylation of proteins. Mutations in this gene have been associated with congenital disorder of glycosylation type Ih (CDG-Ih). Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
  • synonyms:
  • NM_024079,
  • HGNC:23161,
  • asparagine-linked glycosylation 8, alpha-1,3-glucosyltransferase homolog (S. cerevisiae),
  • uc001oza.2,
  • OTTHUMG00000166594,
  • dolichyl-P-Glc:Glc(1)Man(9)GlcNAc(2)-PP-dolichol alpha- 1->3-glucosyltransferase,
  • MGC2840,
  • ALG8,
  • CDG1H,
  • asparagine-linked glycosylation 8 homolog (yeast, alpha-1,3-glucosyltransferase),
  • AJ224875,
  • PCLD3
  • identifiers:
  • 79053,
  • ENSG00000159063,
  • ALG8

Genome feature

Region: gene ? Length: 38712  
Location: 11:78100942-78139653 reverse strand Cyto location: 11q14.1


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Disease

2 Diseases

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2011 SN Ps

5 Cross References

20 Data Sets

7 Homologues

0 Located Features

90 Rna Seq Results