Alg9 alpha-1,2-mannosyltransferase

Preferred Label : Alg9 alpha-1,2-mannosyltransferase;

Symbol : ALG9;

CISMeF acronym : ALG9;

Type : Gene;

Alternative titles and symbols : Alg9, s. cerevisiae, homolog of; Disrupted in bipolar disorder 1; DIBD1;

Ensembl ID : ENSG00000086848;

Prefixed ID : *606941;

Details

Origin ID

606941;

UMLS CUI

C1538263;

Automatic exact mappings (from CISMeF team)
- ALG9 alpha-1,2-mannosyltransferase [ORDO Gene]
- ALG9 alpha-1,2-mannosyltransferase [HGNC gene]
HGNC gene
- ALG9 alpha-1,2-mannosyltransferase [HGNC gene]
ORDO concept(s)
- ALG9 alpha-1,2-mannosyltransferase [ORDO Gene]
Phenotypes related
- Congenital disorder of glycosylation, type il [OMIM Phenotype]
- Gillessen-kaesbach-nishimura syndrome [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- ALG9 alpha-1,2-mannosyltransferase [HGNC gene]

Keyword's position in hierarchy(ies) :

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