FGFR2

GPTKB entity

Statements (66)
Predicate Object
gptkbp:instanceOf gptkb:protein
gptkb:gene
gptkbp:alias gptkb:CEK2
gptkb:K-sam
gptkb:KGFR
gptkb:TK14
gptkb:BEK
gptkb:JWS
gptkb:CD332
gptkbp:alternativeSplicing produces multiple isoforms
gptkbp:encodes gptkb:FGFR2_protein
gptkbp:Entrez_Gene_ID gptkb:ENSG00000066468
2263
gptkbp:expressedIn gptkb:cancer
mammary gland
stomach
intestine
epithelial cells
developing limb
mesenchymal cells
craniofacial tissue
gptkbp:fullName gptkb:Fibroblast_growth_factor_receptor_2
gptkbp:function gptkb:receptor_tyrosine_kinase
binds fibroblast growth factors
gptkbp:geneType protein-coding
gptkbp:HGNC_ID gptkb:HGNC:3689
https://www.w3.org/2000/01/rdf-schema#label FGFR2
gptkbp:interactsWith gptkb:PIK3R1
gptkb:PLCγ
gptkb:SHC1
gptkb:FGF1
gptkb:FGF2
gptkb:FGF7
gptkb:GRB2
gptkb:FGF10
gptkb:FRS2
gptkbp:involvedIn cell differentiation
cell proliferation
embryonic development
gptkbp:locatedOnChromosome 10
gptkbp:location gptkb:10q26
gptkbp:MIM_gene 176943
gptkbp:mutationAssociatedWith gptkb:cancer
gptkb:Antley-Bixler_syndrome
gptkb:Apert_syndrome
gptkb:Beare-Stevenson_cutis_gyrata_syndrome
gptkb:Crouzon_syndrome
gptkb:Jackson-Weiss_syndrome
gptkb:endometrial_cancer
gptkb:Pfeiffer_syndrome
cholangiocarcinoma
gastric cancer
gptkbp:OMIM 176943
gptkbp:organism gptkb:Homo_sapiens
gptkbp:orthologIn gptkb:mouse_Fgfr2
gptkb:zebrafish_fgfr2
gptkbp:pathway gptkb:RAS_signaling_pathway
gptkb:MAPK_signaling_pathway
gptkb:PI3K-Akt_signaling_pathway
gptkb:FGF_signaling_pathway
gptkbp:PDB gptkb:1EV2
gptkb:2PSQ
gptkb:2PVF
gptkbp:UniProtID gptkb:P21802
gptkbp:bfsParent gptkb:Lenvima
gptkbp:bfsLayer 5