Nicotinamide nucleotide adenylyltransferase 1

Preferred Label : Nicotinamide nucleotide adenylyltransferase 1;

Symbol : NMNAT1;

CISMeF acronym : NMNAT1;

Type : Gene;

Alternative titles and symbols : Pyridine nucleotide adenylyltransferase 1; NMNAT; PNAT1;

Ensembl ID : ENSG00000173614;

Prefixed ID : *608700;

Details

Origin ID

608700;

UMLS CUI

C1425150;

Automatic exact mappings (from CISMeF team)
- nicotinamide nucleotide adenylyltransferase 1 [ORDO Gene]
- nicotinamide nucleotide adenylyltransferase 1 [HGNC gene]
HGNC gene
- nicotinamide nucleotide adenylyltransferase 1 [HGNC gene]
ORDO concept(s)
- nicotinamide nucleotide adenylyltransferase 1 [ORDO Gene]
Phenotypes related
- Leber congenital amaurosis 9 [OMIM Phenotype]
- Spondyloepiphyseal dysplasia, sensorineural hearing loss, impaired intellectual development, and leber congenital amaurosis [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- nicotinamide nucleotide adenylyltransferase 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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