Retinoic acid-induced gene 1

Preferred Label : Retinoic acid-induced gene 1;

Symbol : RAI1;

CISMeF acronym : RAI1;

Type : Gene;

Alternative titles and symbols : Retinoic acid-inducible 1;

Ensembl ID : ENSG00000108557;

Prefixed ID : *607642;

Details

Origin ID

607642;

UMLS CUI

C1419249;

Automatic exact mappings (from CISMeF team)
- GPRC5A wt Allele [NCIt concept]
- RAI1 Gene [NCIt concept]
- RAI1 gene [LOINC component]
- RAI1 wt Allele [NCIt concept]
- retinoic acid induced 1 [HGNC gene]
- retinoic acid induced 1 [ORDO Gene]
- ribonuclease A family member 12 (inactive) [HGNC gene]
HGNC gene
- retinoic acid induced 1 [HGNC gene]
NCIt concept(s)
- Retinoic Acid-Induced Protein 1 [NCIt concept]
ORDO concept(s)
- retinoic acid induced 1 [ORDO Gene]
Phenotypes related
- Smith-magenis syndrome [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- RAI1 Gene [NCIt concept]
- RAI1 gene [LOINC component]
- retinoic acid induced 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients