FGFR4
Fibroblast growth factor receptor 4
Also known as: CD334, FGFR4_HUMAN, JTK2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P22455
- Gene
- FGFR4
- Ensembl
- ENSG00000160867
- Chromosome
- 5
- Canonical length
- 802 aa
- Protein class
- Cancer-related genes, CD markers, Disease related genes, Enzymes, FDA approved drug targets, Plasma proteins, Predicted intracellular proteins, Predicted membrane proteins, RAS pathway related proteins, Transporters
- Secretome location
- Intracellular and membrane
- Quaternary structure
- Homodimer
OverviewNCBI Gene
The protein encoded by this gene is a tyrosine kinase and cell surface receptor for fibroblast growth factors. The encoded protein is involved in the regulation of several pathways, including cell proliferation, cell differentiation, cell migration, lipid metabolism, bile acid biosynthesis, vitamin D metabolism, glucose uptake, and phosphate homeostasis. This protein consists of an extracellular region, composed of three immunoglobulin-like domains, a single hydrophobic membrane-spanning segment, and a cytoplasmic tyrosine kinase domain. The extracellular portion interacts with fibroblast growth factors, setting in motion a cascade of downstream signals, ultimately influencing mitogenesis and differentiation. [provided by RefSeq, Aug 2017]
Canonical amino-acid sequenceUniProt
802 residues, UniProt reviewed canonical sequence.
>P22455|FGFR4
1 MRLLLALLGV LLSVPGPPVL SLEASEEVEL EPCLAPSLEQ QEQELTVALG QPVRLCCGRA
61 ERGGHWYKEG SRLAPAGRVR GWRGRLEIAS FLPEDAGRYL CLARGSMIVL QNLTLITGDS
121 LTSSNDDEDP KSHRDPSNRH SYPQQAPYWT HPQRMEKKLH AVPAGNTVKF RCPAAGNPTP
181 TIRWLKDGQA FHGENRIGGI RLRHQHWSLV MESVVPSDRG TYTCLVENAV GSIRYNYLLD
241 VLERSPHRPI LQAGLPANTT AVVGSDVELL CKVYSDAQPH IQWLKHIVIN GSSFGADGFP
301 YVQVLKTADI NSSEVEVLYL RNVSAEDAGE YTCLAGNSIG LSYQSAWLTV LPEEDPTWTA
361 AAPEARYTDI ILYASGSLAL AVLLLLAGLY RGQALHGRHP RPPATVQKLS RFPLARQFSL
421 ESGSSGKSSS SLVRGVRLSS SGPALLAGLV SLDLPLDPLW EFPRDRLVLG KPLGEGCFGQ
481 VVRAEAFGMD PARPDQASTV AVKMLKDNAS DKDLADLVSE MEVMKLIGRH KNIINLLGVC
541 TQEGPLYVIV ECAAKGNLRE FLRARRPPGP DLSPDGPRSS EGPLSFPVLV SCAYQVARGM
601 QYLESRKCIH RDLAARNVLV TEDNVMKIAD FGLARGVHHI DYYKKTSNGR LPVKWMAPEA
661 LFDRVYTHQS DVWSFGILLW EIFTLGGSPY PGIPVEELFS LLREGHRMDR PPHCPPELYG
721 LMRECWHAAP SQRPTFKQLV EALDKVLLAV SEEYLDLRLT FGPYSPSGGD ASSTCSSSDS
781 VFSHDPLPLG SSSFPFGSGV QTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against FGFR4 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.39
- Highest tissue expression
- 82 nTPM
Expression across tissuesHPA
Tissue
- liver: 82 nTPM
- lung: 63 nTPM
- kidney: 40 nTPM
- pancreas: 28 nTPM
- ovary: 27 nTPM
- spleen: 22 nTPM
Single-cell type
- tuft cells: 150 nCPM
- myosatellite cells: 107 nCPM
- cholangiocytes: 96 nCPM
- pancreatic duct cells: 47 nCPM
- podocytes: 43 nCPM
- enteric stem cells: 43 nCPM
Immune cell
- memory B-cell: 0.2 nTPM
- basophil: 0.1 nTPM
- neutrophil: 0.1 nTPM
- plasmacytoid DC: 0.1 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
Brain region
- cerebellum: 5.8 nTPM
- cerebral cortex: 3.8 nTPM
- choroid plexus: 3 nTPM
- hippocampal formation: 3 nTPM
- basal ganglia: 2.8 nTPM
- white matter: 2.8 nTPM
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)
- 0.87
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.19
- DepMap mean gene effect
- 0.03
- DepMap dependency class
- selective
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
- cell migration
- cholesterol homeostasis
- fibroblast growth factor receptor signaling pathway
- glucose homeostasis
- peptidyl-tyrosine phosphorylation
- phosphate ion homeostasis
- positive regulation of catalytic activity
- positive regulation of cell population proliferation
- positive regulation of DNA biosynthetic process
- positive regulation of ERK1 and ERK2 cascade
- positive regulation of gene expression
- positive regulation of proteolysis
- protein autophosphorylation
- regulation of bile acid biosynthetic process
- regulation of extracellular matrix disassembly
- regulation of lipid metabolic process
Molecular functions
- ATP binding
- fibroblast growth factor binding
- fibroblast growth factor receptor activity
- heparin binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Protein kinase domain
- Serine-threonine/tyrosine-protein kinase, catalytic domain
- Immunoglobulin subtype 2
- Immunoglobulin domain subtype
- Immunoglobulin-like domain
- Tyrosine-protein kinase, active site
- Protein kinase-like domain superfamily
- Immunoglobulin I-set
- Immunoglobulin-like fold
- Fibroblast growth factor receptor family
- Protein kinase, ATP binding site
- Tyrosine-protein kinase, catalytic domain
- Immunoglobulin-like domain superfamily
- Receptor Tyrosine Kinase
- Immunoglobulin I-set domain
- Protein tyrosine and serine/threonine kinase
- Immunoglobulin domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of FGFR4 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 FGFR4 as an antibody target. Whether an autoantibody or antibody against FGFR4 could matter depends on whether native FGFR4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
FGFR4 is annotated at the cell surface, where native FGFR4 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label FGFR4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...