TNFAIP1
BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 2
Also known as: B12, B61, BACD2_HUMAN, BTBD34, EDP1, MGC2317
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q13829
- Gene
- TNFAIP1
- Ensembl
- ENSG00000109079
- Chromosome
- 17
- Canonical length
- 316 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoli
OverviewNCBI Gene
This gene was identified as a gene whose expression can be induced by the tumor necrosis factor alpha (TNF) in umbilical vein endothelial cells. Studies of a similar gene in mouse suggest that the expression of this gene is developmentally regulated in a tissue-specific manner. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
316 residues, UniProt reviewed canonical sequence.
>Q13829|TNFAIP1
1 MSGDTCLCPA SGAKPKLSGF KGGGLGNKYV QLNVGGSLYY TTVRALTRHD TMLKAMFSGR
61 MEVLTDKEGW ILIDRCGKHF GTILNYLRDD TITLPQNRQE IKELMAEAKY YLIQGLVNMC
121 QSALQDKKDS YQPVCNIPII TSLKEEERLI ESSTKPVVKL LYNRSNNKYS YTSNSDDHLL
181 KNIELFDKLS LRFNGRVLFI KDVIGDEICC WSFYGQGRKL AEVCCTSIVY ATEKKQTKVE
241 FPEARIYEET LNVLLYETPR VPDNSLLEAT SRSRSQASPS EDEETFELRD RVRRIHVKRY
301 STYDDRQLGH QSTHRDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TNFAIP1 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.37
- Highest tissue expression
- 47 nTPM
Expression across tissuesHPA
Tissue
- liver: 47 nTPM
- spleen: 47 nTPM
- heart muscle: 42 nTPM
- placenta: 42 nTPM
- lung: 38 nTPM
- esophagus: 37 nTPM
Single-cell type
- esophageal apical cells: 100 nCPM
- syncytiotrophoblasts: 93 nCPM
- vascular endothelial cells: 79 nCPM
- lymphatic endothelial cells: 78 nCPM
- esophageal suprabasal cells: 72 nCPM
- alveolar cells type 1: 66 nCPM
Immune cell
- eosinophil: 9.5 nTPM
- myeloid DC: 9.3 nTPM
- NK-cell: 9.2 nTPM
- non-classical monocyte: 8.7 nTPM
- MAIT T-cell: 7.8 nTPM
- classical monocyte: 7.2 nTPM
Brain region
- choroid plexus: 59 nTPM
- thalamus: 54 nTPM
- amygdala: 46 nTPM
- cerebral cortex: 45 nTPM
- medulla oblongata: 42 nTPM
- midbrain: 41 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)
- 0.64
- gnomAD pLI
- 0.14
- gnomAD missense Z
- 1.53
- DepMap mean gene effect
- 0.02
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- apoptotic process
- cell migration
- immune response
- negative regulation of Rho protein signal transduction
- positive regulation of DNA replication
- proteasome-mediated ubiquitin-dependent protein catabolic process
- protein homooligomerization
- protein ubiquitination
- stress fiber assembly
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TNFAIP1 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 TNFAIP1 as an antibody target. Whether an autoantibody or antibody against TNFAIP1 could matter depends on whether native TNFAIP1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TNFAIP1 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label TNFAIP1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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