ALG12 alpha-1,6-mannosyltransferase

Preferred Label : ALG12 alpha-1,6-mannosyltransferase;

Approved symbol HGNC : ALG12;

Name synonyms HGNC : dol-P-Man dependent alpha-1; dolichyl-P-Man:Man(7)GlcNAc(2)-PP-dolichol alpha-1; 6-mannosyltransferase; 6-mannosyltransferase;

Alias symbols HGNC : CDG1G; ECM39;

Chromosome HGNC : 22q13.33;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000182858;

Details

Origin ID

HGNC:19358;

UMLS CUI

C1426190;

Automatic exact mappings (from CISMeF team)
- ALG12 alpha-1,6-mannosyltransferase [ORDO Gene]
- Alg12 alpha-1,6-mannosyltransferase [OMIM gene]
NCIt concept
- ALG12 Gene [NCIt concept]
OMIM gene
- Alg12 alpha-1,6-mannosyltransferase [OMIM gene]
Orphanet gene
- ALG12 alpha-1,6-mannosyltransferase [ORDO Gene]
See also inter- (CISMeF)
- Congenital disorder of glycosylation, type ig [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- ALG12 Gene [NCIt concept]
- Alg12 alpha-1,6-mannosyltransferase [OMIM gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients