TNFRSF12A
Tumor necrosis factor receptor superfamily member 12A
Also known as: CD266, FN14, TNR12_HUMAN, TweakR
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NP84
- Gene
- TNFRSF12A
- Ensembl
- ENSG00000006327
- Chromosome
- 16
- Canonical length
- 129 aa
- Protein class
- Cancer-related genes, CD markers, Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Plasma membrane,Cytosol
OverviewNCBI Gene
Involved in positive regulation of extrinsic apoptotic signaling pathway and regulation of wound healing. Predicted to be located in cell surface and ruffle. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
129 residues, UniProt reviewed canonical sequence.
>Q9NP84|TNFRSF12A
1 MARGSLRRLL RLLVLGLWLA LLRSVAGEQA PGTAPCSRGS SWSADLDKCM DCASCRARPH
61 SDFCLGCAAA PPAPFRLLWP ILGGALSLTF VLGLLSGFLV WRRCRRREKF TTPIEETGGE
121 GCPAVALIQLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TNFRSF12A 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)
- 0.52
- Highest tissue expression
- 147 nTPM
Expression across tissuesHPA
Tissue
- blood vessel: 147 nTPM
- pancreas: 110 nTPM
- heart muscle: 109 nTPM
- kidney: 96 nTPM
- choroid plexus: 82 nTPM
- lung: 76 nTPM
Single-cell type
- epididymal basal cells: 901 nCPM
- fallopian secretory cells: 707 nCPM
- pancreatic duct cells: 588 nCPM
- alveolar cells type 1: 535 nCPM
- epididymal efferent duct ciliated cells: 450 nCPM
- basal keratinocytes: 437 nCPM
Immune cell
- eosinophil: 140 nTPM
- neutrophil: 103 nTPM
- myeloid DC: 15 nTPM
- basophil: 12 nTPM
- classical monocyte: 12 nTPM
- NK-cell: 8 nTPM
Brain region
- thalamus: 14 nTPM
- cerebral cortex: 13 nTPM
- choroid plexus: 11 nTPM
- hypothalamus: 11 nTPM
- midbrain: 9.3 nTPM
- medulla oblongata: 9.2 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)
- 1.53
- gnomAD pLI
- 0.02
- gnomAD missense Z
- -0.14
- DepMap mean gene effect
- -0.05
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- angiogenesis
- cell differentiation
- extrinsic apoptotic signaling pathway
- positive regulation of apoptotic process
- positive regulation of axon extension
- positive regulation of extrinsic apoptotic signaling pathway
- regulation of angiogenesis
- regulation of wound healing
- substrate-dependent cell migration, cell attachment to substrate
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Tumour necrosis factor receptor 12
- Tumour necrosis factor receptor stn_TNFRSF12A_TNFR domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TNFRSF12A 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 TNFRSF12A as an antibody target. Whether an autoantibody or antibody against TNFRSF12A could matter depends on whether native TNFRSF12A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TNFRSF12A is annotated at the cell surface, where native TNFRSF12A 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 TNFRSF12A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...