Reelin - CISMeF

Preferred Label : Reelin;

Symbol : RELN;

CISMeF acronym : RELN;

Type : Gene;

Alternative titles and symbols : RL;

Ensembl ID : ENSG00000189056;

Prefixed ID : *600514;

Details

Origin ID

600514;

UMLS CUI

C1419337;

Automatic exact mappings (from CISMeF team)
- RELN Gene [NCIt concept]
- RELN wt Allele [NCIt concept]
- Reelin [NCIt concept]
- reelin [ORDO Gene]
- reelin [HGNC gene]
HGNC gene
- reelin [HGNC gene]
NCIt concept(s)
- RELN Gene [NCIt concept]
- RELN wt Allele [NCIt concept]
- Reelin [NCIt concept]
ORDO concept(s)
- reelin [ORDO Gene]
Phenotypes related
- Epilepsy, familial temporal lobe, 7 [OMIM Phenotype]
- Lissencephaly 2 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- RELN Gene [NCIt concept]
- reelin [HGNC gene]

Keyword's position in hierarchy(ies) :

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