C1QTNF3
Complement C1q tumor necrosis factor-related protein 3
Also known as: 2310005P21Rik, C1QT3_HUMAN, Corcs, Cors, Cors-26, CTRP3
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BXJ4
- Gene
- C1QTNF3
- Ensembl
- ENSG00000082196
- Chromosome
- 5
- Canonical length
- 246 aa
- Protein class
- Plasma proteins, Predicted secreted proteins
- Subcellular location
- Golgi apparatus
- Secretome location
- Secreted to blood
OverviewNCBI Gene
Enables identical protein binding activity. Involved in several processes, including intracellular triglyceride homeostasis; negative regulation of non-canonical NF-kappaB signal transduction; and regulation of cytokine production. Acts upstream of or within negative regulation of gluconeogenesis. Located in extracellular exosome and membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
246 residues, UniProt reviewed canonical sequence.
>Q9BXJ4|C1QTNF3
1 MLWRQLIYWQ LLALFFLPFC LCQDEYMESP QTGGLPPDCS KCCHGDYSFR GYQGPPGPPG
61 PPGIPGNHGN NGNNGATGHE GAKGEKGDKG DLGPRGERGQ HGPKGEKGYP GIPPELQIAF
121 MASLATHFSN QNSGIIFSSV ETNIGNFFDV MTGRFGAPVS GVYFFTFSMM KHEDVEEVYV
181 YLMHNGNTVF SMYSYEMKGK SDTSSNHAVL KLAKGDEVWL RMGNGALHGD HQRFSTFAGF
241 LLFETKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against C1QTNF3 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)
- 0.48
- Highest tissue expression
- 49 nTPM
Expression across tissuesHPA
Tissue
- salivary gland: 49 nTPM
- esophagus: 31 nTPM
- retina: 22 nTPM
- smooth muscle: 22 nTPM
- urinary bladder: 12 nTPM
- colon: 11 nTPM
Single-cell type
- bergmann glia: 40 nCPM
- oligodendrocytes: 32 nCPM
- oligodendrocyte progenitor cells: 20 nCPM
- choroid plexus epithelial cells: 12 nCPM
- astrocytes: 11 nCPM
- ependymal cells: 10 nCPM
Immune cell
- basophil: 0.3 nTPM
- MAIT T-cell: 0.1 nTPM
- naive B-cell: 0.1 nTPM
- naive CD8 T-cell: 0.1 nTPM
- neutrophil: 0.1 nTPM
- classical monocyte: 0 nTPM
Brain region
- hypothalamus: 11 nTPM
- cerebellum: 10 nTPM
- spinal cord: 8.3 nTPM
- medulla oblongata: 7.2 nTPM
- white matter: 6.6 nTPM
- basal ganglia: 6.5 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)
- 1.28
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.1
- DepMap mean gene effect
- 0.11
- 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
- fat cell differentiation
- intracellular triglyceride homeostasis
- negative regulation of gene expression
- negative regulation of gluconeogenesis
- negative regulation of inflammatory response
- negative regulation of interleukin-6 production
- negative regulation of monocyte chemotactic protein-1 production
- negative regulation of non-canonical NF-kappaB signal transduction
- positive regulation of adiponectin secretion
- positive regulation of cytokine production
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads C1QTNF3 as an antibody target. Whether an autoantibody or antibody against C1QTNF3 could matter depends on whether native C1QTNF3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
C1QTNF3 is annotated as secreted, so native C1QTNF3 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 C1QTNF3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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