CX3CR1
CX3C chemokine receptor 1
Also known as: CCRL1, CMKBRL1, CMKDR1, CX3C1_HUMAN, GPR13, V28
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P49238
- Gene
- CX3CR1
- Ensembl
- ENSG00000168329
- Chromosome
- 3
- Canonical length
- 355 aa
- Protein class
- Disease related genes, G-protein coupled receptors, Human disease related genes, Plasma proteins, Potential drug targets, Predicted membrane proteins
- Subcellular location
- Plasma membrane
OverviewNCBI Gene
Fractalkine is a transmembrane protein and chemokine involved in the adhesion and migration of leukocytes. The protein encoded by this gene is a receptor for fractalkine. The encoded protein also is a coreceptor for HIV-1, and some variations in this gene lead to increased susceptibility to HIV-1 infection and rapid progression to AIDS. Four transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jan 2010]
Canonical amino-acid sequenceUniProt
355 residues, UniProt reviewed canonical sequence.
>P49238|CX3CR1
1 MDQFPESVTE NFEYDDLAEA CYIGDIVVFG TVFLSIFYSV IFAIGLVGNL LVVFALTNSK
61 KPKSVTDIYL LNLALSDLLF VATLPFWTHY LINEKGLHNA MCKFTTAFFF IGFFGSIFFI
121 TVISIDRYLA IVLAANSMNN RTVQHGVTIS LGVWAAAILV AAPQFMFTKQ KENECLGDYP
181 EVLQEIWPVL RNVETNFLGF LLPLLIMSYC YFRIIQTLFS CKNHKKAKAI KLILLVVIVF
241 FLFWTPYNVM IFLETLKLYD FFPSCDMRKD LRLALSVTET VAFSHCCLNP LIYAFAGEKF
301 RRYLYHLYGK CLAVLCGRSV HVDFSSSESQ RSRHGSVLSS NFTYHTSDGD ALLLLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CX3CR1 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
- 7
- Mean surface accessibility (rSASA)
- 0.34
- Highest tissue expression
- 33 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 33 nTPM
- midbrain: 12 nTPM
- spleen: 11 nTPM
- spinal cord: 11 nTPM
- lung: 9.3 nTPM
- amygdala: 7.1 nTPM
Single-cell type
- microglia: 937 nCPM
- nk-cells: 104 nCPM
- macrophages: 41 nCPM
- cdc: 35 nCPM
- monocytes: 21 nCPM
- t-cells: 9 nCPM
Immune cell
- non-classical monocyte: 451 nTPM
- gdT-cell: 265 nTPM
- intermediate monocyte: 261 nTPM
- total PBMC: 233 nTPM
- memory CD8 T-cell: 145 nTPM
- naive CD8 T-cell: 123 nTPM
Brain region
- white matter: 63 nTPM
- spinal cord: 52 nTPM
- medulla oblongata: 47 nTPM
- thalamus: 43 nTPM
- pons: 40 nTPM
- midbrain: 33 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about CX3CR1.
Disease | AllUniProt
Conditions CX3CR1 is implicated in, by any mechanism.
- Macular degeneration, age-related, 12 (ARMD12) MIM:613784
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)
- 1.01
- gnomAD pLI
- 0.06
- gnomAD missense Z
- 1.08
- DepMap mean gene effect
- 0.03
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- adaptive immune response
- antifungal innate immune response
- autocrine signaling
- brain development
- calcium-mediated signaling
- cell adhesion
- cell chemotaxis
- cell-cell signaling
- cellular defense response
- cellular response to lipopolysaccharide
- central nervous system maturation
- chemotaxis
- G protein-coupled receptor signaling pathway
- host-mediated modulation of intestinal microbiota composition
- immune response
- innate immune response
- leukocyte chemotaxis
- leukocyte tethering or rolling
- microglial cell activation involved in immune response
- modulation of chemical synaptic transmission
- negative regulation of angiogenesis
- negative regulation of apoptotic signaling pathway
- negative regulation of hippocampal neuron apoptotic process
- negative regulation of interleukin-1 beta production
- phospholipase C-activating G protein-coupled receptor signaling pathway
- positive regulation of canonical NF-kappaB signal transduction
- positive regulation of cytosolic calcium ion concentration
- positive regulation of monocyte chemotaxis
- positive regulation of neuroblast proliferation
- positive regulation of neurogenesis
- positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction
- regulation of microglial cell migration
- regulation of neurogenesis
- regulation of nitric oxide biosynthetic process
- regulation of synaptic plasticity
- regulation of tumor necrosis factor production
- response to ischemia
- response to wounding
- social behavior
- synapse maturation
- synapse pruning
- multiple spine synapse organization, single dendrite
- negative regulation of microglial cell mediated cytotoxicity
Molecular functions
- C-C chemokine binding
- C-C chemokine receptor activity
- chemokine receptor activity
- CX3C chemokine receptor binding
- G protein-coupled peptide receptor activity
- G protein-coupled receptor activity
- C-X3-C chemokine binding
- C-X3-C chemokine receptor activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CX3CR1 as an antibody target. Whether an autoantibody or antibody against CX3CR1 could matter depends on whether native CX3CR1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CX3CR1 is annotated at the cell surface, where native CX3CR1 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 CX3CR1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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