Platelet-derived growth factor receptor, beta

Preferred Label : Platelet-derived growth factor receptor, beta;

Symbol : PDGFRB;

CISMeF acronym : PDGFRB;

Type : Gene;

Alternative titles and symbols : PDGFR; PDGFR1;

Included titles and symbols : Pdgfrb/etv6 fusion gene; Pdgfrb/d10s170 fusion gene; Pdgfrb/rabpt5 fusion gene; Pdgfrb/hip1 fusion gene; Pdgfrb/myo18a fusion gene;

Ensembl ID : ENSG00000113721;

Prefixed ID : *173410;

Détails

Origin ID

173410;

UMLS CUI

C1335202;

Automatic exact mappings (from CISMeF team)
- CCDC6/PDGFRB Fusion Gene [NCIt concept]
- ETV6/PDGFRB Fusion Gene [NCIt concept]
- HIP1/PDGFRB Fusion Gene [NCIt concept]
- MYO18A/PDGFRB Fusion Gene [NCIt concept]
- PDGFRB Gene [NCIt concept]
- PDGFRB gene [LOINC component]
- PDGFRB wt Allele [NCIt concept]
- PDGFRB/MYO18A Fusion Gene [NCIt concept]
- Platelet-Derived Growth Factor Receptor [NCIt concept]
- Platelet-Derived Growth Factor Receptor Beta [NCIt concept]
- RABEP1/PDGFRB Fusion Gene [NCIt concept]
- platelet derived growth factor receptor beta [ORDO Gene]
- platelet derived growth factor receptor beta [HGNC gene]
- receptor, Platelet-Derived growth factor beta [MeSH concept]
- receptor, platelet-derived growth factor beta [MeSH Descriptor]
HGNC gene
- platelet derived growth factor receptor beta [HGNC gene]
NCIt concept(s)
- PDGFRB Gene [NCIt concept]
- PDGFRB wt Allele [NCIt concept]
- Platelet-Derived Growth Factor Receptor Beta [NCIt concept]
ORDO concept(s)
- platelet derived growth factor receptor beta [ORDO Gene]
Phenotypes related
- Basal ganglia calcification, idiopathic, 4 [OMIM Phenotype]
- Kosaki overgrowth syndrome [OMIM Phenotype]
- Myofibromatosis, infantile, 1 [OMIM Phenotype]
- Premature aging syndrome, penttinen type [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- PDGFRB Gene [NCIt concept]
- PDGFRB gene [LOINC component]
- platelet derived growth factor receptor beta [HGNC gene]

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