TFPT
TCF3 fusion partner
Also known as: amida, FB1, INO80F, TFPT_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P0C1Z6
- Gene
- TFPT
- Ensembl
- ENSG00000105619
- Chromosome
- 19
- Canonical length
- 253 aa
- Protein class
- Disease related genes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Predicted to enable DNA binding activity. Involved in several processes, including apoptotic signaling pathway; chromatin remodeling; and regulation of nucleobase-containing compound metabolic process. Located in nucleoplasm. Part of Ino80 complex. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
253 residues, UniProt reviewed canonical sequence.
>P0C1Z6|TFPT
1 MELEQREGTM AAVGFEEFSA PPGSELALPP LFGGHILESE LETEVEFVSG GLGGSGLRER
61 DEEEEAARGR RRRQRELNRR KYQALGRRCR EIEQVNERVL NRLHQVQRIT RRLQQERRFL
121 MRVLDSYGDD YRASQFTIVL EDEGSQGTDA PTPGNAENEP PEKETLSPPR RTPAPPEPGS
181 PAPGEGPSGR KRRRVPRDGR RAGNALTPEL APVQIKVEED FGFEADEALD SSWVSRGPDK
241 LLPYPTLASP ASDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TFPT 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)
- 0.64
- Highest tissue expression
- 90 nTPM
Expression across tissuesHPA
Tissue
- amygdala: 90 nTPM
- cerebral cortex: 81 nTPM
- hippocampal formation: 68 nTPM
- midbrain: 47 nTPM
- basal ganglia: 45 nTPM
- hypothalamus: 40 nTPM
Single-cell type
- hofbauer cells: 154 nCPM
- gastric chief cells: 66 nCPM
- megakaryocytes: 62 nCPM
- mucous neck cells: 47 nCPM
- gastric progenitor cells: 42 nCPM
- melanocytes: 39 nCPM
Immune cell
- plasmacytoid DC: 43 nTPM
- T-reg: 26 nTPM
- NK-cell: 21 nTPM
- memory CD8 T-cell: 20 nTPM
- memory CD4 T-cell: 19 nTPM
- myeloid DC: 19 nTPM
Brain region
- cerebral cortex: 28 nTPM
- white matter: 28 nTPM
- amygdala: 27 nTPM
- hippocampal formation: 25 nTPM
- midbrain: 23 nTPM
- hypothalamus: 21 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)
- 1.12
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.46
- DepMap mean gene effect
- -0.08
- 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
- apoptotic signaling pathway
- chromatin remodeling
- DNA recombination
- DNA repair
- positive regulation of apoptotic process
- positive regulation of DNA repair
- positive regulation of DNA-templated transcription
- positive regulation of telomere maintenance in response to DNA damage
- regulation of cell cycle
- regulation of chromosome organization
- regulation of DNA repair
- regulation of DNA replication
- regulation of DNA strand elongation
- regulation of embryonic development
- telomere maintenance
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- TCF3 fusion partner
- INO80 complex subunit F
- INO80 complex subunit F
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TFPT 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 TFPT as an antibody target. Whether an autoantibody or antibody against TFPT could matter depends on whether native TFPT is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TFPT 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 TFPT as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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