FGF2 (Fibroblast Growth Factor 2) Gene

Key regulator of angiogenesis, cell growth, and tissue repair

Gene Information Card

Symbol FGF2
Full Name Fibroblast growth factor 2
Gene Type protein-coding
Chromosomal Location 4q28.1
NCBI Gene ID 2247 ncbi.nlm.nih.gov/gene/2247
Ensembl ID ENSG00000138685
UniProt ID P09038
OMIM ID 134920
HGNC ID 3676
Aliases bFGF, FGFB, HBGF-2

Description

FGF2 (fibroblast growth factor 2) encodes a member of the fibroblast growth factor (FGF) family. The encoded protein is a potent mitogen and angiogenic factor involved in embryonic development, cell growth, morphogenesis, tissue repair, and tumor growth. FGF2 binds to FGF receptors (FGFRs) and heparan sulfate proteoglycans to initiate signaling cascades.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Cancer (multiple types) Overexpression of FGF2 promotes angiogenesis and tumor growth via autocrine/paracrine signaling COSMIC, ClinVar
Coronary artery disease FGF2 polymorphisms associated with altered angiogenic response OMIM, NCBI
Retinopathy of prematurity Elevated FGF2 contributes to pathological neovascularization ClinVar, literature
Skeletal dysplasias FGF2 signaling dysregulation linked to abnormal bone growth OMIM

Expression Profile

Tissue Expression
Tissue nTPM level
Brain 12.3 Medium
Heart 8.7 Low
Lung 15.2 Medium
Liver 6.1 Low
Kidney 10.5 Medium
Placenta 22.8 High
Cell Line Expression
Cell Line nTPM Notes
HeLa 18.4 Cervical cancer cell line
A549 14.2 Lung cancer cell line
MCF7 9.8 Breast cancer cell line
HUVEC 25.6 Endothelial cells, high expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1A>G Missense <0.1% Reduced protein stability
c.472C>T Nonsense <0.1% Premature truncation, loss of function
c.614G>A Missense <0.1% Altered receptor binding affinity
Mutation functional classification

Loss of Function (LOF)

Nonsense and frameshift mutations leading to truncated protein or reduced activity.

Gain of Function (GOF)

Missense mutations that enhance receptor binding or protein stability, observed in some cancers.

Dominant Negative (DN)

Not well documented for FGF2; most mutations are recessive or neutral.

Pathways

FGF signaling pathway (KEGG: hsa04010)
MAPK signaling pathway (KEGG: hsa04010)
PI3K-Akt signaling pathway (KEGG: hsa04151)
Ras signaling pathway (KEGG: hsa04014)

Protein Summary

FGF2 (basic fibroblast growth factor, bFGF) is a 18-24 kDa heparin-binding growth factor. It exists in multiple isoforms due to alternative initiation of translation. The protein lacks a classical signal peptide and is secreted via an unconventional pathway. FGF2 binds to FGFR1-4 and heparan sulfate, activating downstream pathways including MAPK, PI3K/Akt, and PLCγ. It plays critical roles in angiogenesis, wound healing, and embryonic development. Dysregulation is implicated in cancer and vascular diseases.

Related Products

Product name Cat.No. Species Gene ID
FGF20 Knockout HEK293 Cell Line EDJ-KQ661 Human 26281 Details Get a Quote
FGF23 Knockout HEK293 Cell Line EDJ-KQ662 Human 8074 Details Get a Quote
FGF2 Knockout HEK293 Cell Line EDJ-KQ17695 Human 2247 Details Get a Quote
FGF21 Knockout HEK293 Cell Line EDJ-KQ17774 Human 26291 Details Get a Quote
FGF2 Knockout A-549 Cell Line EDJ-KQ19169 Human 2247 Details Get a Quote
FGF2 Knockout HCT 116 Cell Line EDJ-KQ19170 Human 2247 Details Get a Quote
FGF2 Knockout HeLa Cell Line EDJ-KQ19171 Human 2247 Details Get a Quote
FGF23 Knockout HeLa Cell Line EDJ-KQ18297 Human 8074 Details Get a Quote
FGF22 Knockout HEK293 Cell Line EDJ-KQ51196 Human 27006 Details Get a Quote
FGF20 Knockout HeLa Cell Line EDJ-KQ55920 Human 26281 Details Get a Quote
FGF21 Knockout HeLa Cell Line EDJ-KQ55926 Human 26291 Details Get a Quote
FGF22 Knockout HeLa Cell Line EDJ-KQ55980 Human 27006 Details Get a Quote
FGF23 Knockout A-549 Cell Line EDJ-KQ63309 Human 8074 Details Get a Quote
FGF20 Knockout A-549 Cell Line EDJ-KQ64410 Human 26281 Details Get a Quote
FGF21 Knockout A-549 Cell Line EDJ-KQ64414 Human 26291 Details Get a Quote
Displaying Records 1 To 15 Of 21 Records
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