TFF2
Trefoil factor 2
Also known as: SML1, TFF2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q03403
- Gene
- TFF2
- Ensembl
- ENSG00000160181
- Chromosome
- 21
- Canonical length
- 129 aa
- Protein class
- Cancer-related genes, Predicted secreted proteins
- Secretome location
- Secreted to digestive system
OverviewNCBI Gene
Members of the trefoil family are characterized by having at least one copy of the trefoil motif, a 40-amino acid domain that contains three conserved disulfides. They are stable secretory proteins expressed in gastrointestinal mucosa. Their functions are not defined, but they may protect the mucosa from insults, stabilize the mucus layer and affect healing of the epithelium. The encoded protein inhibits gastric acid secretion. This gene and two other related trefoil family member genes are found in a cluster on chromosome 21. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
129 residues, UniProt reviewed canonical sequence.
>Q03403|TFF2
1 MGRRDAQLLA ALLVLGLCAL AGSEKPSPCQ CSRLSPHNRT NCGFPGITSD QCFDNGCCFD
61 SSVTGVPWCF HPLPKQESDQ CVMEVSDRRN CGYPGISPEE CASRKCCFSN FIFEVPWCFF
121 PKSVEDCHYLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TFF2 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)
- 0.37
- Highest tissue expression
- 6,463 nTPM
Expression across tissuesHPA
Tissue
- stomach: 6,463 nTPM
- duodenum: 1,343 nTPM
- gallbladder: 99 nTPM
- pancreas: 20 nTPM
- rectum: 3.9 nTPM
- liver: 3.8 nTPM
Single-cell type
- foveolar cells: 11,063 nCPM
- cholangiocytes: 1,686 nCPM
- mucous neck cells: 777 nCPM
- gastric chief cells: 611 nCPM
- gastric progenitor cells: 431 nCPM
- pancreatic duct cells: 214 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- amygdala: 0 nTPM
- basal ganglia: 0 nTPM
- cerebellum: 0 nTPM
- cerebral cortex: 0 nTPM
- choroid plexus: 0 nTPM
- hippocampal formation: 0 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)
- 1.89
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.46
- DepMap mean gene effect
- 0.17
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- chemokine-mediated signaling pathway
- maintenance of gastrointestinal epithelium
- negative regulation of gastric acid secretion
Molecular functions
- CXCR4 chemokine receptor binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TFF2 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 TFF2 as an antibody target. Whether an autoantibody or antibody against TFF2 could matter depends on whether native TFF2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TFF2 is annotated as secreted, so native TFF2 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 TFF2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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