Gene Gene information from NCBI Gene database.
Entrez ID 26281
Gene name Fibroblast growth factor 20
Gene symbol FGF20
Synonyms (NCBI Gene)
FGF-20RHDA2
Chromosome 8
Chromosome location 8p22
Summary The protein encoded by this gene is a member of the fibroblast growth factor family. The fibroblast growth factors possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes including embryonic development,
SNPs SNP information provided by dbSNP.
2
SNP ID Visualize variation Clinical significance Consequence
rs587777282 C>- Pathogenic Frameshift variant, coding sequence variant
rs1585100306 C>T Likely-pathogenic Splice acceptor variant
miRNA miRNA information provided by mirtarbase database.
6
miRTarBase ID miRNA Experiments Reference
MIRT001741 hsa-miR-433-3p Luciferase reporter assayWestern blot 18252210
MIRT001741 hsa-miR-433-3p Luciferase reporter assay 18252210
MIRT001741 hsa-miR-433-3p Other 18252210
MIRT2229346 hsa-miR-1236 CLIP-seq
MIRT2229347 hsa-miR-587 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
31
GO ID Ontology Definition Evidence Reference
GO:0005102 Function Signaling receptor binding TAS 11306498
GO:0005104 Function Fibroblast growth factor receptor binding IBA
GO:0005104 Function Fibroblast growth factor receptor binding IEA
GO:0005576 Component Extracellular region IEA
GO:0005576 Component Extracellular region TAS 10913340
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
605558 3677 ENSG00000078579
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NP95
Protein name Fibroblast growth factor 20 (FGF-20)
Protein function Neurotrophic factor that regulates central nervous development and function.
PDB 3F1R
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00167 FGF 65 191 Fibroblast growth factor Domain
Tissue specificity TISSUE SPECIFICITY: Predominantly expressed in the cerebellum. {ECO:0000269|PubMed:11306498}.
Sequence
Sequence length 211
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  MAPK signaling pathway
Ras signaling pathway
Rap1 signaling pathway
Calcium signaling pathway
PI3K-Akt signaling pathway
Regulation of actin cytoskeleton
Pathways in cancer
Chemical carcinogenesis - receptor activation
Melanoma
Breast cancer
Gastric cancer
  PI3K Cascade
PIP3 activates AKT signaling
Signaling by activated point mutants of FGFR1
Signaling by activated point mutants of FGFR3
FGFR4 ligand binding and activation
FGFR3b ligand binding and activation
FGFR3c ligand binding and activation
FGFR1c ligand binding and activation
FGFR2c ligand binding and activation
FGFR3 mutant receptor activation
Activated point mutants of FGFR2
Constitutive Signaling by Aberrant PI3K in Cancer
Phospholipase C-mediated cascade: FGFR1
Phospholipase C-mediated cascade; FGFR2
Phospholipase C-mediated cascade; FGFR3
Phospholipase C-mediated cascade; FGFR4
Downstream signaling of activated FGFR1
SHC-mediated cascade:FGFR1
PI-3K cascade:FGFR1
FRS-mediated FGFR1 signaling
PI-3K cascade:FGFR2
SHC-mediated cascade:FGFR2
FRS-mediated FGFR2 signaling
SHC-mediated cascade:FGFR3
FRS-mediated FGFR3 signaling
PI-3K cascade:FGFR3
FRS-mediated FGFR4 signaling
SHC-mediated cascade:FGFR4
PI-3K cascade:FGFR4
Negative regulation of FGFR1 signaling
Negative regulation of FGFR2 signaling
Negative regulation of FGFR3 signaling
Negative regulation of FGFR4 signaling
Signaling by FGFR2 in disease
Signaling by FGFR1 in disease
RAF/MAP kinase cascade
PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling
Signaling by FGFR3 point mutants in cancer
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
17
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Renal hypodysplasia/aplasia 2 Pathogenic; Likely pathogenic rs587777282, rs1585100306 RCV000114397
RCV000988038
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
EBV-positive nodal T- and NK-cell lymphoma Likely benign rs1451460296 RCV004560275
FGF20-related disorder Likely benign; Benign rs377477340, rs1443350894, rs1402726873, rs112951749, rs1258624500, rs112352647, rs1304371939, rs1483812834, rs796448091, rs373023438, rs377326763, rs3793405 RCV003963346
RCV003909261
RCV003929728
RCV003929743
RCV003897305
RCV003972063
RCV003939304
RCV003979034
RCV003976616
RCV003962244
RCV003958279
RCV004757326
Parkinson disease, late-onset Benign rs12720208 RCV000005162
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Asthma Associate 36255742
Bovine Respiratory Disease Complex Associate 18252210
Depressive Disorder Associate 30241547
Disease Progression Inhibit 34193611
Kidney Failure Chronic Inhibit 34193611
Malocclusion Angle Class III Associate 28640125
Neurodegenerative Diseases Associate 27341347
Parkinson Disease Associate 15122513, 18252210, 19133659, 23394771, 26535683, 33349842
Squamous Cell Carcinoma of Head and Neck Associate 34051764