Neurexin I - CISMeF

Preferred Label : Neurexin I;

Symbol : NRXN1;

CISMeF acronym : NRXN1;

Type : Gene;

Ensembl ID : ENSG00000179915;

Prefixed ID : *600565;

Details

Origin ID

600565;

UMLS CUI

C1417851;

Automatic exact mappings (from CISMeF team)
- NRXN1 Gene [NCIt concept]
- Neurexin-1 [NCIt concept]
- neurexin 1 [HGNC gene]
- neurexin 1 [ORDO Gene]
HGNC gene
- neurexin 1 [HGNC gene]
NCIt concept(s)
- NRXN1 Gene [NCIt concept]
- NRXN1 wt Allele [NCIt concept]
- Neurexin-1 [NCIt concept]
- Neurexin-1-Beta [NCIt concept]
ORDO concept(s)
- neurexin 1 [ORDO Gene]
Phenotypes related
- Chromosome 2p16.3 deletion syndrome [OMIM Phenotype]
- Pitt-hopkins-like syndrome 2 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- NRXN1 Gene [NCIt concept]
- neurexin 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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