CGAS
Cyclic GMP-AMP synthase
Also known as: C6orf150, CGAS_HUMAN, h-cGAS, MB21D1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8N884
- Gene
- CGAS
- Ensembl
- ENSG00000164430
- Chromosome
- 6
- Canonical length
- 522 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nuclear bodies,Cytosol
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Enables several functions, including 2',3'-cyclic GMP-AMP synthase activity; molecular condensate scaffold activity; and phosphatidylinositol-4,5-bisphosphate binding activity. Involved in several processes, including intracellular signal transduction; paracrine signaling; and regulation of defense response. Located in nuclear body; plasma membrane; and site of double-strand break. Is active in cytosol and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
522 residues, UniProt reviewed canonical sequence.
>Q8N884|CGAS
1 MQPWHGKAMQ RASEAGATAP KASARNARGA PMDPTESPAA PEAALPKAGK FGPARKSGSR
61 QKKSAPDTQE RPPVRATGAR AKKAPQRAQD TQPSDATSAP GAEGLEPPAA REPALSRAGS
121 CRQRGARCST KPRPPPGPWD VPSPGLPVSA PILVRRDAAP GASKLRAVLE KLKLSRDDIS
181 TAAGMVKGVV DHLLLRLKCD SAFRGVGLLN TGSYYEHVKI SAPNEFDVMF KLEVPRIQLE
241 EYSNTRAYYF VKFKRNPKEN PLSQFLEGEI LSASKMLSKF RKIIKEEIND IKDTDVIMKR
301 KRGGSPAVTL LISEKISVDI TLALESKSSW PASTQEGLRI QNWLSAKVRK QLRLKPFYLV
361 PKHAKEGNGF QEETWRLSFS HIEKEILNNH GKSKTCCENK EEKCCRKDCL KLMKYLLEQL
421 KERFKDKKHL DKFSSYHVKT AFFHVCTQNP QDSQWDRKDL GLCFDNCVTY FLQCLRTEKL
481 ENYFIPEFNL FSSNLIDKRS KEFLTKQIEY ERNNEFPVFD EFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CGAS 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
- 0
- Mean surface accessibility (rSASA)
- 0.41
- Highest tissue expression
- 13 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 13 nTPM
- lymph node: 6.9 nTPM
- appendix: 6 nTPM
- spleen: 5.2 nTPM
- tonsil: 4.4 nTPM
- urinary bladder: 4 nTPM
Single-cell type
- monocyte progenitors: 110 nCPM
- neutrophils: 109 nCPM
- neutrophil progenitors: 104 nCPM
- monocytes: 85 nCPM
- plasma cells: 66 nCPM
- macrophages: 51 nCPM
Immune cell
- basophil: 26 nTPM
- eosinophil: 19 nTPM
- plasmacytoid DC: 18 nTPM
- intermediate monocyte: 18 nTPM
- classical monocyte: 13 nTPM
- non-classical monocyte: 12 nTPM
Brain region
- white matter: 6.8 nTPM
- thalamus: 6.6 nTPM
- cerebral cortex: 6.3 nTPM
- pons: 5.5 nTPM
- medulla oblongata: 5.3 nTPM
- spinal cord: 5.2 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)
- 1.29
- gnomAD pLI
- 0
- DepMap mean gene effect
- -0.12
- 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
- activation of innate immune response
- cellular response to exogenous dsRNA
- cGAS/STING signaling pathway
- cytoplasmic pattern recognition receptor signaling pathway
- defense response to virus
- determination of adult lifespan
- DNA damage response
- DNA repair
- innate immune response
- negative regulation of cGAS/STING signaling pathway
- negative regulation of double-strand break repair via homologous recombination
- paracrine signaling
- pattern recognition receptor signaling pathway
- positive regulation of cellular senescence
- positive regulation of defense response to virus by host
- positive regulation of type I interferon production
- regulation of immunoglobulin production
- regulation of T cell activation
Molecular functions
- ATP binding
- chromatin binding
- DNA binding
- double-stranded DNA binding
- GTP binding
- metal ion binding
- molecular condensate scaffold activity
- nucleosome binding
- phosphatidylinositol-4,5-bisphosphate binding
- poly-ADP-D-ribose modification-dependent protein binding
- protein homodimerization activity
- 2',3'-cyclic GMP-AMP synthase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
- Acetylation
- ADP-ribosylation
- Antiviral defense
- ATP-binding
- Cell membrane
- Chromosome
- Cytoplasm
- DNA damage
- DNA repair
- DNA-binding
- GTP-binding
- Host-virus interaction
- Immunity
- Innate immunity
- Isopeptide bond
- Lipid-binding
- Lipoprotein
- Magnesium
- Membrane
- Metal-binding
- Methylation
- Nucleotide-binding
- Nucleotidyltransferase
- Nucleus
- Palmitate
- Phosphoprotein
- Transferase
- Ubl conjugation
- Zinc
InteractionsUniProt · HPA
Protein binding partners of CGAS 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 CGAS as an antibody target. Whether an autoantibody or antibody against CGAS could matter depends on whether native CGAS is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CGAS is annotated at the cell surface, where native CGAS 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 CGAS as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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