Fibroblast growth factor receptor 1

Preferred Label : Fibroblast growth factor receptor 1;

Symbol : FGFR1;

CISMeF acronym : FGFR1;

Type : Gene;

Alternative titles and symbols : Fms-like tyrosine kinase 2; Fms-like gene; FLT2; FLG;

Included titles and symbols : Fgfr1/bcr fusion gene; Fgfr1/fgfr1op2 fusion gene; Fgfr1/znf198 fusion gene; Fgfr1/tacc1 fusion gene;

Ensembl ID : ENSG00000077782;

Prefixed ID : *136350;

Details

Origin ID

136350;

UMLS CUI

C0919509;

Automatic exact mappings (from CISMeF team)
- BCR/FGFR1 Fusion Gene [NCIt concept]
- FGFR1 Gene [NCIt concept]
- FGFR1 gene [LOINC component]
- FGFR1 wt Allele [NCIt concept]
- FGFR1OP2/FGFR1 Fusion Gene [NCIt concept]
- FLG Gene [NCIt concept]
- Fibroblast Growth Factor Receptor 1 [NCIt concept]
- ZMYM2/FGFR1 Fusion Gene [NCIt concept]
- fibroblast growth factor receptor 1 [ORDO Gene]
- fibroblast growth factor receptor 1 [HGNC gene]
- receptor, fibroblast growth factor, type 1 [MeSH Descriptor]
HGNC gene
- fibroblast growth factor receptor 1 [HGNC gene]
NCIt concept(s)
- FGFR1 Gene [NCIt concept]
- FGFR1 wt Allele [NCIt concept]
- Fibroblast Growth Factor Receptor 1 [NCIt concept]
ORDO concept(s)
- fibroblast growth factor receptor 1 [ORDO Gene]
Phenotypes related
- Encephalocraniocutaneous lipomatosis [OMIM Phenotype]
- Hartsfield syndrome [OMIM Phenotype]
- Hypogonadotropic hypogonadism 2 with or without anosmia [OMIM Phenotype]
- Jackson-weiss syndrome [OMIM Phenotype]
- Osteoglophonic dysplasia [OMIM Phenotype]
- Pfeiffer syndrome [OMIM Phenotype]
- Trigonocephaly 1 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- FGFR1 Gene [NCIt concept]
- FGFR1 gene [LOINC component]
- fibroblast growth factor receptor 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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