Oncogene FGR - CISMeF

Preferred Label : Oncogene FGR;

NCIt definition : Human Oncogene FGR is a mutated variant of FGR Gene (SRC Family), which encodes 529-aa 60-kDa p55-FGR, a protein tyrosine kinase that may bind PTPNS1 and contains 1 SH2 and 1 SH3 domain. Oncogene FGR disrupts normal cell function.;

NCI Metathesaurus CUI : CL448407;

GenBank Accession Number : M19722;

Details

Origin ID

C18333;

UMLS CUI

C0919478;

Currated CISMeF NLP mapping
- FGR proto-oncogene, Src family tyrosine kinase [HGNC gene]
- Fgr protooncogene, src family tyrosine kinase [OMIM gene]
OMIM relation
- Fgr protooncogene, src family tyrosine kinase [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- FGR proto-oncogene, Src family tyrosine kinase [HGNC gene]
- Fgr protooncogene, src family tyrosine kinase [OMIM gene]
allele_in_chromosomal_location
- 1p36.2-p36.1 [NCIt concept]
gene_found_in_organism
- Human [NCIt concept]
gene_plays_role_in_process
- Protein Phosphorylation Process [NCIt concept]
- Signal Transduction [NCIt concept]
- Tumorigenesis [NCIt concept]
- Tyrosine Phosphorylation [NCIt concept]

Keyword's position in hierarchy(ies) :

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