ALG2 alpha-1,3/1,6-mannosyltransferase

Preferred Label : ALG2 alpha-1,3/1,6-mannosyltransferase;

Approved symbol HGNC : ALG2;

Alias symbols HGNC : FLJ14511; CDGIi; hALPG2; NET38; CDG1I;

Chromosome HGNC : 9q22.33;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000119523;

Details

Origin ID

HGNC:23159;

UMLS CUI

C1427955;

Automatic exact mappings (from CISMeF team)
- ALG2 alpha-1,3/1,6-mannosyltransferase [ORDO Gene]
- Alg2 alpha-1,3/1,6-mannosyltransferase [OMIM gene]
OMIM gene
- Alg2 alpha-1,3/1,6-mannosyltransferase [OMIM gene]
Orphanet gene
- ALG2 alpha-1,3/1,6-mannosyltransferase [ORDO Gene]
See also inter- (CISMeF)
- Congenital disorder of glycosylation, type II [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- Alg2 alpha-1,3/1,6-mannosyltransferase [OMIM gene]

Keyword's position in hierarchy(ies) :

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