FGFBP3

gene
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Also known as MGC39320

Summary

FGFBP3 (fibroblast growth factor binding protein 3, HGNC:23428) is a protein-coding gene on chromosome 10q23.32, encoding Fibroblast growth factor-binding protein 3 (Q8TAT2). Heparin-binding protein which binds to FGF2, prevents binding of FGF2 to heparin and probably inhibits immobilization of FGF2 on extracellular matrix glycosaminoglycans, allowing its release and subsequent activation of FGFR signaling which leads to increased vascular permeabili….

Enables fibroblast growth factor binding activity and heparin binding activity. Acts upstream of or within positive regulation of fibroblast growth factor receptor signaling pathway and positive regulation of vascular permeability. Located in extracellular region.

Source: NCBI Gene 143282 — RefSeq curated summary.

At a glance

  • GWAS associations: 2
  • Clinical variants (ClinVar): 54 total
  • MANE Select transcript: NM_152429

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:23428
Approved symbolFGFBP3
Namefibroblast growth factor binding protein 3
Location10q23.32
Locus typegene with protein product
StatusApproved
AliasesMGC39320
Ensembl geneENSG00000174721
Ensembl biotypeprotein_coding
OMIM620879
Entrez143282

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000311575

RefSeq mRNA: 1 — MANE Select: NM_152429 NM_152429

CCDS: CCDS7418

Canonical transcript exons

ENST00000311575 — 2 exons

ExonStartEnd
ENSE000011979559190939891909486
ENSE000013380959190658491909047

Expression profiles

Bgee: expression breadth ubiquitous, 165 present calls, max score 98.42.

FANTOM5 (CAGE): breadth broad, TPM avg 3.9852 / max 168.0918, expressed in 344 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
1106443.6032342
1106430.3820142

Top tissues by expression

232 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
ventricular zoneUBERON:000305398.42gold quality
embryoUBERON:000092295.52gold quality
ganglionic eminenceUBERON:000402395.52gold quality
cortical plateUBERON:000534386.21gold quality
dorsal root ganglionUBERON:000004481.38gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099180.61gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047377.61silver quality
buccal mucosa cellCL:000233677.06gold quality
trigeminal ganglionUBERON:000167575.00gold quality
anterior cingulate cortexUBERON:000983573.25gold quality
amygdalaUBERON:000187672.98gold quality
hypothalamusUBERON:000189872.95gold quality
C1 segment of cervical spinal cordUBERON:000646971.48gold quality
prefrontal cortexUBERON:000045171.31gold quality
right frontal lobeUBERON:000281070.10gold quality
spinal cordUBERON:000224070.05gold quality
neocortexUBERON:000195070.04gold quality
dorsolateral prefrontal cortexUBERON:000983469.60gold quality
nucleus accumbensUBERON:000188269.32gold quality
putamenUBERON:000187469.19gold quality
Brodmann (1909) area 9UBERON:001354068.97gold quality
cerebral cortexUBERON:000095668.78gold quality
frontal cortexUBERON:000187068.52gold quality
frontal lobeUBERON:001652568.52gold quality
forebrainUBERON:000189067.87gold quality
tibial nerveUBERON:000132367.74gold quality
caudate nucleusUBERON:000187367.71gold quality
hindlimb stylopod muscleUBERON:000425267.66gold quality
brainUBERON:000095567.61gold quality
pigmented layer of retinaUBERON:000178267.08silver quality

Single-cell (SCXA)

Detected in 8 experiment(s), a significant marker in 6.

ExperimentMarker?Max mean expression
E-HCAD-56yes1483.39
E-GEOD-93593yes1130.72
E-MTAB-10485yes717.07
E-MTAB-10018yes639.49
E-MTAB-8894yes629.35
E-HCAD-5yes43.56
E-MTAB-6524no258.04
E-ANND-3no1.63

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

66 targeting FGFBP3, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):

miRNAMax scoreAvg scoremiRNA target_count
HSA-MIR-5011-5P100.0083.465820
HSA-MIR-190A-3P100.0080.355520
HSA-MIR-3646100.0073.565283
HSA-MIR-8485100.0077.574731
HSA-MIR-3925-3P100.0069.951237
HSA-MIR-371B-5P99.9975.344759
HSA-MIR-548C-3P99.9974.017587
HSA-MIR-373-5P99.9875.364753
HSA-MIR-616-5P99.9875.584775
HSA-MIR-50799.9770.111915
HSA-MIR-314899.9775.066478
HSA-MIR-3688-3P99.9772.022834
HSA-MIR-6888-3P99.9765.951170
HSA-MIR-55799.9670.011640
HSA-MIR-6825-5P99.9669.813431
HSA-MIR-365899.9673.874379
HSA-MIR-6744-5P99.9366.82748
HSA-MIR-568099.9169.833421
HSA-MIR-6780A-5P99.8866.692776
HSA-MIR-3663-3P99.8470.39798
HSA-MIR-4799-5P99.8270.602663
HSA-MIR-6739-5P99.8067.872806
HSA-MIR-4668-5P99.7970.583782
HSA-MIR-1273H-5P99.7766.322471
HSA-MIR-30B-3P99.7065.762325
HSA-MIR-3689A-3P99.7065.732306
HSA-MIR-3689B-3P99.7065.712311
HSA-MIR-3689C99.7065.712311
HSA-MIR-6779-5P99.7065.762363
HSA-MIR-472999.6972.184233

Literature-anchored findings (GeneRIF, showing 1)

  • the FGF binding domain and the heparin binding domain are necessary for the hBP3 interaction with endogenous FGF and the activation of FGFR signaling in vivo (PMID:18669637)

Cross-species orthologs

3 orthologs

OrganismSymbolGene ID
danio_reriofgfbp3ENSDARG00000040162
mus_musculusFgfbp3ENSMUSG00000047632
rattus_norvegicusFgfbp3ENSRNOG00000022796

Paralogs (2): FGFBP1 (ENSG00000137440), FGFBP2 (ENSG00000137441)

Protein

Protein identifiers

Fibroblast growth factor-binding protein 3Q8TAT2 (reviewed: Q8TAT2)

All UniProt accessions (1): Q8TAT2

UniProt curated annotations — full annotation on UniProt →

Function. Heparin-binding protein which binds to FGF2, prevents binding of FGF2 to heparin and probably inhibits immobilization of FGF2 on extracellular matrix glycosaminoglycans, allowing its release and subsequent activation of FGFR signaling which leads to increased vascular permeability.

Subunit / interactions. Interacts with FGF2.

Subcellular location. Secreted.

Similarity. Belongs to the fibroblast growth factor-binding protein family.

RefSeq proteins (1): NP_689642* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR010510FGF1-bdFamily

Pfam: PF06473

UniProt features (10 total): disulfide bond 3, compositionally biased region 2, sequence variant 2, signal peptide 1, chain 1, region of interest 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q8TAT2-F169.020.32

Functional residue map

Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.

Disulfide bonds (3): 59–80, 90–124, 241–249

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

IDPathway
R-HSA-190377FGFR2b ligand binding and activation

MSigDB gene sets: 116 (showing top): FXR_IR1_Q6, GOBP_REGULATION_OF_CELLULAR_RESPONSE_TO_GROWTH_FACTOR_STIMULUS, GOBP_CIRCULATORY_SYSTEM_PROCESS, REACTOME_SIGNALING_BY_FGFR, GOBP_CELL_CELL_SIGNALING, NKX61_01, GOBP_RESPONSE_TO_FIBROBLAST_GROWTH_FACTOR, GOBP_REGULATION_OF_FIBROBLAST_GROWTH_FACTOR_RECEPTOR_SIGNALING_PATHWAY, WTGAAAT_UNKNOWN, SCHAEFFER_PROSTATE_DEVELOPMENT_6HR_UP, GOBP_POSITIVE_REGULATION_OF_VASCULAR_PERMEABILITY, GOMF_GLYCOSAMINOGLYCAN_BINDING, TATA_C, GOBP_RESPONSE_TO_GROWTH_FACTOR, LASTOWSKA_NEUROBLASTOMA_COPY_NUMBER_DN

GO Biological Process (3): cell-cell signaling (GO:0007267), positive regulation of vascular permeability (GO:0043117), positive regulation of fibroblast growth factor receptor signaling pathway (GO:0045743)

GO Molecular Function (3): heparin binding (GO:0008201), fibroblast growth factor binding (GO:0017134), growth factor binding (GO:0019838)

GO Cellular Component (2): extracellular region (GO:0005576), extracellular matrix (GO:0031012)

Reactome top-level categories

Rollup of top-1 pathways:

CategoryPathways
FGFR2 ligand binding and activation1

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
cell communication1
signaling1
regulation of vascular permeability1
fibroblast growth factor receptor signaling pathway1
positive regulation of signal transduction1
regulation of fibroblast growth factor receptor signaling pathway1
glycosaminoglycan binding1
sulfur compound binding1
growth factor binding1
protein binding1
cellular anatomical structure1
external encapsulating structure1

Protein interactions and networks

STRING

576 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
FGFBP3ARHGEF33A8MVX0476
FGFBP3HDHD3Q9BSH5469
FGFBP3MDFIC2A0A1B0GVS7456
FGFBP3DDAH1O94760444
FGFBP3ANO4Q32M45436
FGFBP3ZNF592Q92610433
FGFBP3TTYH1Q9H313418
FGFBP3USP31Q70CQ4410
FGFBP3CDC42BPBQ9Y5S2410
FGFBP3GPC1P35052400
FGFBP3B4GALT3O60512395
FGFBP3MPP3Q13368391
FGFBP3KIF1BO60333387
FGFBP3IDH3AP50213387
FGFBP3SLC25A37Q9NYZ2386

IntAct

0 interactions, top by confidence:

BioGRID (1): FGFBP3 (PCA)

ESM2 similar proteins: A0A140LIA7, A0A1B0GTL2, A2VDX9, A3FFS8, A6NCS6, A8MVW0, K9M1U5, O43541, P01588, P03971, P03972, P07321, P07865, P0C7N4, P0DPE3, P13725, P27106, P29676, P33707, P33708, P33709, P48617, P49000, P49157, P53346, P79295, Q02011, Q0Z956, Q16619, Q1HCM0, Q28513, Q29RM6, Q5BLP8, Q5S1V9, Q60753, Q63086, Q65Z15, Q6H8S9, Q6H8T0, Q6H8T1

Diamond homologs: Q1HCM0, Q8TAT2

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

54 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance52
Likely benign1
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

85 predictions. Top by Δscore:

VariantEffectΔscore
10:91909391:AACTT:Adonor_loss0.9800
10:91909392:ACTTA:Adonor_loss0.9800
10:91909393:CTT:Cdonor_loss0.9800
10:91909394:TTAC:Tdonor_loss0.9800
10:91909395:TACCG:Tdonor_loss0.9800
10:91909396:A:ACdonor_gain0.9800
10:91909396:ACCG:Adonor_loss0.9800
10:91909397:C:Adonor_loss0.9800
10:91909397:C:CCdonor_gain0.9800
10:91909046:ACCT:Aacceptor_loss0.9400
10:91909048:CTGCG:Cacceptor_loss0.9400
10:91909049:T:Gacceptor_loss0.9400
10:91909390:GAACT:Gdonor_loss0.9300
10:91909397:CCGA:Cdonor_gain0.9100
10:91908240:T:TAdonor_gain0.9000
10:91909397:CCG:Cdonor_gain0.8900
10:91909397:CCGAG:Cdonor_gain0.8900
10:91909048:C:CCacceptor_gain0.8800
10:91909396:AC:Adonor_gain0.8800
10:91909397:CC:Cdonor_gain0.8800
10:91907335:TCTC:Tacceptor_gain0.8200
10:91909050:G:Cacceptor_loss0.8200
10:91907334:GTCT:Gacceptor_gain0.8100
10:91909389:TGAAC:Tdonor_loss0.7500
10:91909382:TA:Tdonor_gain0.6800
10:91908195:AG:Adonor_gain0.6700
10:91909038:TCCCC:Tacceptor_gain0.6700
10:91909045:GAC:Gacceptor_gain0.6500
10:91909044:GGAC:Gacceptor_gain0.6400
10:91907336:CTCA:Cacceptor_gain0.6200

AlphaMissense

1631 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
10:91908640:C:AW110C0.993
10:91908640:C:GW110C0.993
10:91908787:C:AW61C0.992
10:91908787:C:GW61C0.992
10:91908235:C:AW245C0.991
10:91908235:C:GW245C0.991
10:91908818:A:CF51C0.989
10:91908224:C:GC249S0.983
10:91908225:A:TC249S0.983
10:91908224:C:TC249Y0.982
10:91908817:G:CF51L0.980
10:91908817:G:TF51L0.980
10:91908818:A:GF51S0.980
10:91908819:A:GF51L0.980
10:91908248:C:GC241S0.979
10:91908249:A:TC241S0.979
10:91908811:G:CS53R0.975
10:91908811:G:TS53R0.975
10:91908813:T:GS53R0.975
10:91908794:C:TC59Y0.973
10:91908566:C:GC135S0.972
10:91908567:A:TC135S0.972
10:91908599:C:GC124S0.972
10:91908600:A:TC124S0.972
10:91908237:A:GW245R0.971
10:91908237:A:TW245R0.971
10:91908248:C:TC241Y0.971
10:91908794:C:GC59S0.970
10:91908795:A:TC59S0.970
10:91908731:C:GC80S0.967

dbSNP variants (sampled 300 via entrez): RS1001369496 (10:91907533 A>AG), RS1002364309 (10:91909166 C>T), RS1002880509 (10:91910429 C>A,T), RS1003176829 (10:91907411 C>T), RS1003314074 (10:91907189 G>A,T), RS1004102542 (10:91909451 G>A,C), RS1004373586 (10:91908868 G>C), RS1004928750 (10:91910640 C>A,T), RS1005612886 (10:91907813 A>C), RS1006452497 (10:91907422 TG>T), RS1006878969 (10:91907015 A>G), RS1006927367 (10:91906588 TAC>T,TACAC), RS1007422550 (10:91906212 G>C,T), RS1008084647 (10:91909986 C>T), RS1009124043 (10:91908241 C>G,T)

Disease associations

OMIM: gene MIM:620879 | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

2 associations (top):

StudyTraitp-value
GCST006585_505Blood protein levels6.000000e-28
GCST90011900_59Serum alkaline phosphatase levels6.000000e-11

EFO canonical traits (1, from GWAS)

EFO IDTrait name
EFO:0004533alkaline phosphatase measurement

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 1 entry (VIP=true, CPIC=false)

CTD chemical–gene interactions

33 total (human), top 30 by PubMed support.

ChemicalActions (top 5)PubMed papers
Valproic Acidincreases expression, affects expression, decreases expression, affects cotreatment8
methylmercuric chlorideincreases expression, affects cotreatment4
trichostatin Aaffects cotreatment, increases expression3
entinostatincreases expression, affects cotreatment2
4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamideaffects cotreatment, increases expression2
Panobinostataffects cotreatment, increases expression2
Tetrachlorodibenzodioxinaffects expression, decreases expression2
propionaldehydeincreases expression1
tris(1,3-dichloro-2-propyl)phosphatedecreases expression1
sodium arsenitedecreases expression1
nutlin 3affects cotreatment, increases expression1
abrinedecreases expression1
dorsomorphinaffects cotreatment, increases expression1
2-(1H-indazol-4-yl)-6-(4-methanesulfonylpiperazin-1-ylmethyl)-4-morpholin-4-ylthieno(3,2-d)pyrimidineincreases response to substance, increases expression1
jinfukangaffects cotreatment, increases expression1
LDN 193189increases expression, affects cotreatment1
Vorinostatdecreases expression1
Arsenicaffects methylation1
Benzo(a)pyrenedecreases methylation1
Camptothecinincreases expression1
Cisplatinaffects cotreatment, increases expression1
Dactinomycinaffects cotreatment, increases expression1
Quercetinincreases expression1
Silicon Dioxideincreases expression1
Smokedecreases expression1
Thimerosaldecreases expression1
Tretinoindecreases expression1
Triclosandecreases expression1
Cyclosporinedecreases expression1
Gold Compoundsincreases expression1

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.