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Gene : ALG9 Homo sapiens

Name  ? ALG9 alpha-1,2-mannosyltransferase Cytological Location  11q23.1
Brief Description  ALG9, alpha-1,2-mannosyltransferase
description  This gene encodes an alpha-1,2-mannosyltransferase enzyme that functions in lipid-linked oligosaccharide assembly. Mutations in this gene result in congenital disorder of glycosylation type Il. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]
  • synonyms:
  • DIBD1,
  • CDG1L,
  • dol-P-Man dependent alpha-1,2-mannosyltransferase,
  • NM_024740,
  • asparagine-linked glycosylation 9 homolog (yeast, alpha 1,2 mannosyltransferase),
  • asparagine-linked glycosylation 9, alpha- 1,2-mannosyltransferase homolog (S. cerevisiae, alpha- 1,2-mannosyltransferase),
  • HGNC:15672,
  • DIBD1,
  • disrupted in bipolar affective disorder 1,
  • dolichyl-P-Man:Man(6)GlcNAc(2)-PP-dolichol alpha-1,2-mannosyltransferase,
  • asparagine-linked glycosylation 9, alpha-1,2-mannosyltransferase homolog (S. cerevisiae),
  • OTTHUMG00000166819,
  • dolichyl-P-Man:Man(8)GlcNAc(2)-PP-dolichol alpha-1,2-mannosyltransferase,
  • GIKANIS,
  • ALG9,
  • uc031yet.2,
  • LOH11CR1J
  • identifiers:
  • 79796,
  • ENSG00000086848,
  • ALG9

Genome feature

Region: gene ? Length: 95486  
Location: 11:111776096-111871581 reverse strand Cyto location: 11q23.1


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Disease

2 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

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Other

171 SN Ps

5 Cross References

19 Data Sets

9 Homologues

0 Located Features

90 Rna Seq Results