FGF9
Fibroblast growth factor 9
Also known as: FGF9_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P31371
- Gene
- FGF9
- Ensembl
- ENSG00000102678
- Chromosome
- 13
- Canonical length
- 208 aa
- Protein class
- Cancer-related genes, Disease related genes, Human disease related genes, Predicted intracellular proteins, Predicted secreted proteins, RAS pathway related proteins
- Secretome location
- Secreted in other tissues
- Quaternary structure
- Homodimer
OverviewNCBI Gene
The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This protein was isolated as a secreted factor that exhibits a growth-stimulating effect on cultured glial cells. In nervous system, this protein is produced mainly by neurons and may be important for glial cell development. Expression of the mouse homolog of this gene was found to be dependent on Sonic hedgehog (Shh) signaling. Mice lacking the homolog gene displayed a male-to-female sex reversal phenotype, which suggested a role in testicular embryogenesis. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
208 residues, UniProt reviewed canonical sequence.
>P31371|FGF9
1 MAPLGEVGNY FGVQDAVPFG NVPVLPVDSP VLLSDHLGQS EAGGLPRGPA VTDLDHLKGI
61 LRRRQLYCRT GFHLEIFPNG TIQGTRKDHS RFGILEFISI AVGLVSIRGV DSGLYLGMNE
121 KGELYGSEKL TQECVFREQF EENWYNTYSS NLYKHVDTGR RYYVALNKDG TPREGTRTKR
181 HQKFTHFLPR PVDPDKVPEL YKDILSQSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against FGF9 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.39
- Highest tissue expression
- 11 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 11 nTPM
- kidney: 10 nTPM
- retina: 7.6 nTPM
- adrenal gland: 3.9 nTPM
- cerebral cortex: 3.8 nTPM
- heart muscle: 2.5 nTPM
Single-cell type
- müller glia: 223 nCPM
- renal collecting duct intercalated cells: 130 nCPM
- distal convoluted tubule cells: 100 nCPM
- retinal ganglion cells: 97 nCPM
- loop of henle epithelial cells: 77 nCPM
- endometrial luminal cells: 68 nCPM
Immune cell
- naive B-cell: 0.3 nTPM
- memory CD4 T-cell: 0.2 nTPM
- memory CD8 T-cell: 0.2 nTPM
- MAIT T-cell: 0.1 nTPM
- memory B-cell: 0.1 nTPM
- naive CD4 T-cell: 0.1 nTPM
Brain region
- cerebellum: 13 nTPM
- cerebral cortex: 12 nTPM
- pons: 9.4 nTPM
- medulla oblongata: 6.9 nTPM
- thalamus: 6.7 nTPM
- white matter: 5.1 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about FGF9.
Disease | AllUniProt
Conditions FGF9 is implicated in, by any mechanism.
- Multiple synostoses syndrome 3 (SYNS3) MIM:612961
Disease | GeneticClinVar
5 pathogenic / likely-pathogenic of 155 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Multiple synostoses syndrome 3
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.32
- gnomAD pLI
- 0.95
- gnomAD missense Z
- 1.54
- DepMap mean gene effect
- 0.05
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- activin receptor signaling pathway
- angiogenesis
- canonical Wnt signaling pathway
- cardiac muscle cell proliferation
- cell-cell signaling
- chondrocyte differentiation
- embryonic digestive tract development
- embryonic limb morphogenesis
- embryonic skeletal system development
- eye development
- fibroblast growth factor receptor signaling pathway
- inner ear morphogenesis
- lung-associated mesenchyme development
- male gonad development
- male sex determination
- mesenchymal cell proliferation
- negative regulation of transcription by RNA polymerase II
- negative regulation of vascular associated smooth muscle cell differentiation involved in phenotypic switching
- negative regulation of Wnt signaling pathway
- neurogenesis
- osteoblast differentiation
- positive regulation of activin receptor signaling pathway
- positive regulation of canonical Wnt signaling pathway
- positive regulation of cardiac muscle cell proliferation
- positive regulation of cell division
- positive regulation of cell population proliferation
- positive regulation of epithelial cell proliferation
- positive regulation of gene expression
- positive regulation of MAPK cascade
- positive regulation of mesenchymal cell proliferation
- positive regulation of smoothened signaling pathway
- positive regulation of stem cell proliferation
- positive regulation of vascular associated smooth muscle cell migration
- positive regulation of vascular associated smooth muscle cell proliferation
- positive regulation of vascular endothelial growth factor receptor signaling pathway
- protein import into nucleus
- regulation of cell migration
- regulation of timing of cell differentiation
- Sertoli cell proliferation
- signal transduction
- smoothened signaling pathway
- stem cell proliferation
- substantia nigra development
- vascular endothelial growth factor receptor signaling pathway
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of FGF9 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads FGF9 as an antibody target. Whether an autoantibody or antibody against FGF9 could matter depends on whether native FGF9 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
FGF9 is annotated as secreted, so native FGF9 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label FGF9 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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