Beta-1,4-n-acetylgalactosaminyltransferase 1

Preferred Label : Beta-1,4-n-acetylgalactosaminyltransferase 1;

Symbol : B4GALNT1;

CISMeF acronym : B4GALNT1;

Type : Gene;

Alternative titles and symbols : Beta-1,4-n-acetylgalactosaminyltransferase; Gm2/gd2 synthase; GALGT; GalNAcT;

Ensembl ID : ENSG00000135454;

Prefixed ID : *601873;

Details

Origin ID

601873;

UMLS CUI

C1825858;

Automatic exact mappings (from CISMeF team)
- (N-acetylneuraminyl)-galactosylglucosylceramide N-acetylgalactosaminyltransferase [MeSH Supplementary Concept]
- B4GALNT1 Gene [NCIt concept]
- B4GALNT1 wt Allele [NCIt concept]
- Beta-1,4 N-Acetylgalactosaminyltransferase 1 [NCIt concept]
- Polypeptide N-acetylgalactosaminyltransferase [MeSH Descriptor]
- beta-1,4-N-acetyl-galactosaminyltransferase 1 [ORDO Gene]
- beta-1,4-N-acetyl-galactosaminyltransferase 1 [HGNC gene]
HGNC gene
- beta-1,4-N-acetyl-galactosaminyltransferase 1 [HGNC gene]
NCIt concept(s)
- B4GALNT1 Gene [NCIt concept]
- B4GALNT1 wt Allele [NCIt concept]
- Beta-1,4 N-Acetylgalactosaminyltransferase 1 [NCIt concept]
ORDO concept(s)
- beta-1,4-N-acetyl-galactosaminyltransferase 1 [ORDO Gene]
Phenotypes related
- Spastic paraplegia 26, autosomal recessive [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- B4GALNT1 Gene [NCIt concept]
- beta-1,4-N-acetyl-galactosaminyltransferase 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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