retinoic acid induced 1

Preferred Label : retinoic acid induced 1;

Approved symbol HGNC : RAI1;

Alias symbols HGNC : MGC12824; KIAA1820; SMS; DKFZP434A139;

Chromosome HGNC : 17p11.2;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000108557;

Details

Origin ID

HGNC:9834;

UMLS CUI

C1419249;

Automatic exact mappings (from CISMeF team)
- Retinoic acid-induced gene 1 [OMIM gene]
- Smith-magenis syndrome [OMIM Phenotype]
- Spermine synthase [OMIM gene]
- retinoic acid induced 1 [ORDO Gene]
NCIt concept
- RAI1 Gene [NCIt concept]
OMIM gene
- Retinoic acid-induced gene 1 [OMIM gene]
Orphanet gene
- retinoic acid induced 1 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- RAI1 Gene [NCIt concept]
- RAI1 gene [LOINC component]
- Retinoic acid-induced gene 1 [OMIM gene]

Keyword's position in hierarchy(ies) :

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