HCSGD entry for FGFR3
1. General information
Official gene symbol | FGFR3 |
---|---|
Entrez ID | 2261 |
Gene full name | fibroblast growth factor receptor 3 |
Other gene symbols | ACH CD333 CEK2 HSFGFR3EX JTK4 |
Links to Entrez Gene | Links to Entrez Gene |
2. Neighbors in the network
This gene isn't in PPI subnetwork.
3. Gene ontology annotation
GO ID | GO term | Evidence | Category |
---|---|---|---|
GO:0000122 | Negative regulation of transcription from RNA polymerase II promoter | IEA | biological_process |
GO:0000165 | MAPK cascade | IEA | biological_process |
GO:0001501 | Skeletal system development | IEA TAS | biological_process |
GO:0001938 | Positive regulation of endothelial cell proliferation | IEA | biological_process |
GO:0001958 | Endochondral ossification | TAS | biological_process |
GO:0002009 | Morphogenesis of an epithelium | IEA | biological_process |
GO:0002062 | Chondrocyte differentiation | TAS | biological_process |
GO:0002089 | Lens morphogenesis in camera-type eye | IEA | biological_process |
GO:0003416 | Endochondral bone growth | TAS | biological_process |
GO:0004713 | Protein tyrosine kinase activity | IDA | molecular_function |
GO:0005007 | Fibroblast growth factor-activated receptor activity | IEA IMP | molecular_function |
GO:0005515 | Protein binding | IPI | molecular_function |
GO:0005524 | ATP binding | IEA | molecular_function |
GO:0005576 | Extracellular region | IEA | cellular_component |
GO:0005634 | Nucleus | IEA | cellular_component |
GO:0005764 | Lysosome | IEA | cellular_component |
GO:0005783 | Endoplasmic reticulum | IEA | cellular_component |
GO:0005886 | Plasma membrane | TAS | cellular_component |
GO:0005887 | Integral component of plasma membrane | IDA | cellular_component |
GO:0005925 | Focal adhesion | TAS | cellular_component |
GO:0007173 | Epidermal growth factor receptor signaling pathway | TAS | biological_process |
GO:0007259 | JAK-STAT cascade | TAS | biological_process |
GO:0007267 | Cell-cell signaling | IEA | biological_process |
GO:0008284 | Positive regulation of cell proliferation | IEA IGI IMP | biological_process |
GO:0008286 | Insulin receptor signaling pathway | TAS | biological_process |
GO:0008543 | Fibroblast growth factor receptor signaling pathway | IDA IGI TAS | biological_process |
GO:0009898 | Cytoplasmic side of plasma membrane | IEA | cellular_component |
GO:0009986 | Cell surface | IEA | cellular_component |
GO:0010518 | Positive regulation of phospholipase activity | IMP | biological_process |
GO:0016021 | Integral component of membrane | IEA | cellular_component |
GO:0016023 | Cytoplasmic membrane-bounded vesicle | IEA | cellular_component |
GO:0017134 | Fibroblast growth factor binding | IDA IPI | molecular_function |
GO:0018108 | Peptidyl-tyrosine phosphorylation | IDA | biological_process |
GO:0021762 | Substantia nigra development | IEA | biological_process |
GO:0022010 | Central nervous system myelination | IEA | biological_process |
GO:0031398 | Positive regulation of protein ubiquitination | IEA | biological_process |
GO:0035019 | Somatic stem cell maintenance | IEA | biological_process |
GO:0035988 | Chondrocyte proliferation | TAS | biological_process |
GO:0038095 | Fc-epsilon receptor signaling pathway | TAS | biological_process |
GO:0042511 | Positive regulation of tyrosine phosphorylation of Stat1 protein | IMP | biological_process |
GO:0042517 | Positive regulation of tyrosine phosphorylation of Stat3 protein | IMP | biological_process |
GO:0043410 | Positive regulation of MAPK cascade | IMP | biological_process |
GO:0043525 | Positive regulation of neuron apoptotic process | IEA | biological_process |
GO:0043552 | Positive regulation of phosphatidylinositol 3-kinase activity | IMP TAS | biological_process |
GO:0045087 | Innate immune response | TAS | biological_process |
GO:0045597 | Positive regulation of cell differentiation | IEA | biological_process |
GO:0045839 | Negative regulation of mitosis | IEA | biological_process |
GO:0045879 | Negative regulation of smoothened signaling pathway | IEA | biological_process |
GO:0046777 | Protein autophosphorylation | IDA | biological_process |
GO:0048011 | Neurotrophin TRK receptor signaling pathway | TAS | biological_process |
GO:0048015 | Phosphatidylinositol-mediated signaling | TAS | biological_process |
GO:0048471 | Perinuclear region of cytoplasm | IEA | cellular_component |
GO:0048546 | Digestive tract morphogenesis | IEA | biological_process |
GO:0048640 | Negative regulation of developmental growth | ISS | biological_process |
GO:0048678 | Response to axon injury | IEA | biological_process |
GO:0048712 | Negative regulation of astrocyte differentiation | IEA | biological_process |
GO:0050680 | Negative regulation of epithelial cell proliferation | IEA | biological_process |
GO:0060113 | Inner ear receptor cell differentiation | IEA | biological_process |
GO:0060349 | Bone morphogenesis | TAS | biological_process |
GO:0060385 | Axonogenesis involved in innervation | IEA | biological_process |
GO:0061144 | Alveolar secondary septum development | IEA | biological_process |
GO:0070307 | Lens fiber cell development | IEA | biological_process |
GO:0070374 | Positive regulation of ERK1 and ERK2 cascade | IMP | biological_process |
GO:0070977 | Bone maturation | ISS | biological_process |
GO:0072148 | Epithelial cell fate commitment | IEA | biological_process |
GO:0090080 | Positive regulation of MAPKKK cascade by fibroblast growth factor receptor signaling pathway | IEA | biological_process |
GO:0090102 | Cochlea development | IEA | biological_process |
GO:0090263 | Positive regulation of canonical Wnt signaling pathway | IEA | biological_process |
GO:1902178 | Fibroblast growth factor receptor apoptotic signaling pathway | IMP | biological_process |
Entries Per Page
Displaying Page of
4. Expression levels in datasets
- Meta-analysis result
p-value up | p-value down | FDR up | FDR down |
---|---|---|---|
0.8283784469 | 0.1544160252 | 0.9999902473 | 0.7593955726 |
- Individual experiment result
( "-" represent NA in the specific microarray platform )
( "-" represent NA in the specific microarray platform )
Data source | Up or down | Log fold change |
---|---|---|
GSE11954 | Up | 0.1818561321 |
GSE13712_SHEAR | Down | -1.1070059215 |
GSE13712_STATIC | Up | 0.0999070530 |
GSE19018 | Down | -0.5484459144 |
GSE19899_A1 | Up | 0.0175992959 |
GSE19899_A2 | Down | -0.6406574030 |
PubMed_21979375_A1 | Up | 0.1681136039 |
PubMed_21979375_A2 | Down | -0.1963992024 |
GSE35957 | Up | 0.0661444568 |
GSE36640 | Up | 0.0256190015 |
GSE54402 | Down | -0.1137261727 |
GSE9593 | Down | -0.3974878964 |
GSE43922 | Up | 0.0458586752 |
GSE24585 | Up | 0.0130416857 |
GSE37065 | Down | -0.0517493479 |
GSE28863_A1 | Down | -0.1360187952 |
GSE28863_A2 | Up | 0.0531256858 |
GSE28863_A3 | Up | 0.4273670056 |
GSE28863_A4 | Down | -0.0171756717 |
GSE48662 | Up | 0.1025288785 |
5. Regulation relationships with compounds/drugs/microRNAs
- Compounds
Not regulated by compounds
- Drugs
Name | Drug | Accession number |
---|---|---|
Palifermin | DB00039 | BTD00042 | BIOD00042 |
XL999 | DB05014 | - |
Pazopanib | DB06589 | - |
Ponatinib | DB08901 | - |
Lenvatinib | DB09078 | - |
Nintedanib | DB09079 | - |
- MicroRNAs
- mirTarBase
- mirTarBase
MiRNA_name | mirBase ID | miRTarBase ID | Experiment | Support type | References (Pubmed ID) |
---|---|---|---|---|---|
hsa-miR-100-5p | MIMAT0000098 | MIRT003419 | Luciferase reporter assay//qRT-PCR//Western blot | Functional MTI | 19843843 |
hsa-miR-100-5p | MIMAT0000098 | MIRT003419 | Microarray//qRT-PCR//Western blot | Functional MTI | 19396866 |
hsa-miR-99a-5p | MIMAT0000097 | MIRT004243 | Luciferase reporter assay//qRT-PCR//Western blot | Functional MTI | 19843843 |
hsa-miR-99a-5p | MIMAT0000097 | MIRT004243 | Reporter assay;Western blot | Functional MTI | 21383697 |
hsa-miR-26b-5p | MIMAT0000083 | MIRT030099 | Microarray | Functional MTI (Weak) | 19088304 |
Entries Per Page
Displaying Page of
- mirRecord
- mirRecord
MicroRNA name | mirBase ID | Target site number | MiRNA mature ID | Test method inter | MiRNA regulation site | Reporter target site | Pubmed ID |
---|---|---|---|---|---|---|---|
hsa-miR-99a-5p | MIMAT0000097 | NA | hsa-miR-99a | {Western blot} | {downregulation by anti-miRNA oligonucleotide} | 19843843 | |
hsa-miR-100-5p | MIMAT0000098 | NA | hsa-miR-100 | {Western blot} | {downregulation by anti-miRNA oligonucleotide} | 19843843 |
Entries Per Page
Displaying Page of
6. Text-mining results about the gene
Gene occurances in abstracts of cellular senescence-associated articles: 2 abstracts the gene occurs.
PubMed ID of the article | Sentenece the gene occurs |
---|---|
26142204 | Vasodilator responses to acetylcholine (Ach) in the isolated aortic rings were measured, serum concentration of glucose, tumor necrosis factor-alpha (TNF-alpha) and monocyte chemoattractant protein-1 (MCP-1) and the expression of VPO1 in the aorta were determined |
26142204 | RESULTS: Vasodilator responses to Ach were impaired markedly and the serum concentrations of glucose, TNF-alpha and MCP-1 were significantly increased in diabetic rats |
20362703 | FGFR3 signaling induces a reversible senescence phenotype in chondrocytes similar to oncogene-induced premature senescence |
20362703 | In FGFR3-related skeletal dyplasias, oncogenic mutations in the FGFR3 receptor tyrosine kinase cause profound inhibition of cartilage growth resulting in severe dwarfism, although many of the precise mechanisms of FGFR3 action remain unclear |
20362703 | Mutated FGFR3 induces constitutive activation of the ERK pathway in chondrocytes and, remarkably, can also cause both increased proliferation and apoptosis in growing cartilage, depending on the gestational age |
20362703 | Here, we demonstrate that FGFR3 signaling is also capable of inducing premature senescence in chondrocytes, manifested as reversible, ERK-dependent growth arrest accompanied by alteration of cellular shape, loss of the extracellular matrix, upregulation of senescence markers (alpha-GLUCOSIDASE, FIBRONECTIN, CAVEOLIN 1, LAMIN A, SM22alpha and TIMP 1), and induction of senescence-associated beta-GALACTOSIDASE activity |
20362703 | Our data support a model whereby FGFR3 signaling inhibits cartilage growth via exploiting cellular responses originally designed to eliminate cells harboring activated oncogenes |
Entries Per Page
Displaying Page of