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Gene : ALG2 Homo sapiens

Name  ? ALG2 alpha-1,3/1,6-mannosyltransferase Cytological Location  9q22.33
Brief Description  ALG2, alpha-1,3/1,6-mannosyltransferase
description  This gene encodes a member of the glycosyltransferase 1 family. The encoded protein acts as an alpha 1,3 mannosyltransferase, mannosylating Man(2)GlcNAc(2)-dolichol diphosphate and Man(1)GlcNAc(2)-dolichol diphosphate to form Man(3)GlcNAc(2)-dolichol diphosphate. Defects in this gene have been associated with congenital disorder of glycosylation type Ih (CDG-Ii). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2008]
  • synonyms:
  • FLJ14511,
  • hALPG2,
  • CDGIi,
  • CMS14,
  • CMSTA3,
  • CDG1I,
  • asparagine-linked glycosylation 2, alpha-1,3-mannosyltransferase homolog (S. cerevisiae),
  • CDG1I,
  • HGNC:23159,
  • NET38,
  • CDGIi,
  • hALPG2,
  • NM_033087,
  • asparagine-linked glycosylation 2 homolog (yeast, alpha-1,3-mannosyltransferase),
  • NET38,
  • AK027417,
  • OTTHUMG00000020355,
  • uc004azf.4,
  • ALG2
  • identifiers:
  • 85365,
  • ENSG00000119523,
  • ALG2

Genome feature

Region: gene ? Length: 5540  
Location: 9:99216425-99221964 reverse strand Cyto location: 9q22.33


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2 Diseases

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17 SN Ps

5 Cross References

17 Data Sets

7 Homologues

0 Located Features

90 Rna Seq Results