Gephyrin - CISMeF

Preferred Label : Gephyrin;

Symbol : GPHN;

CISMeF acronym : GPHN;

Type : Gene;

Alternative titles and symbols : Gph; GEPH; KIAA1385;

Included titles and symbols : Mll/gphn fusion gene;

Ensembl ID : ENSG00000171723;

Prefixed ID : *603930;

Details

Origin ID

603930;

UMLS CUI

C1423507;

Automatic exact mappings (from CISMeF team)
- GPHN Gene [NCIt concept]
- GPHN wt Allele [NCIt concept]
- Gephyrin [NCIt concept]
- MLL/GPHN Fusion Gene [NCIt concept]
- gephyrin [ORDO Gene]
- gephyrin [MeSH concept]
- gephyrin [MeSH Supplementary Concept]
- gephyrin [HGNC gene]
- guanidinopropionase activity [GO term]
HGNC gene
- gephyrin [HGNC gene]
NCIt concept(s)
- GPHN Gene [NCIt concept]
- GPHN wt Allele [NCIt concept]
- Gephyrin [NCIt concept]
ORDO concept(s)
- gephyrin [ORDO Gene]
Phenotypes related
- Molybdenum Cofactor deficiency, Complementation group C [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- GPHN Gene [NCIt concept]
- gephyrin [HGNC gene]

Keyword's position in hierarchy(ies) :

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