TFIP11
Tuftelin-interacting protein 11
Also known as: DKFZP434B194, Spp382, TFP11_HUMAN, TIP39
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UBB9
- Gene
- TFIP11
- Ensembl
- ENSG00000100109
- Chromosome
- 22
- Canonical length
- 837 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
This gene encodes a protein component of the spliceosome that promotes the release of the lariat-intron during late-stage splicing through the recruitment of a pre-mRNA splicing factor called DEAH-box helicase 15. The encoded protein contains a G-patch domain, a hallmark of RNA-processing proteins, that binds DEAH-box helicase 15. This protein contains an atypical nuclear localization sequence as well as a nuclear speckle-targeting sequence, enabling it to localize to distinct speckled regions within the cell nucleus. Polymorphisms in this gene are associated with dental caries suggesting a role in amelogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016]
Canonical amino-acid sequenceUniProt
837 residues, UniProt reviewed canonical sequence.
>Q9UBB9|TFIP11
1 MSLSHLYRDG EGRIDDDDDE RENFEITDWD LQNEFNPNRQ RHWQTKEEAT YGVWAERDSD
61 DERPSFGGKR ARDYSAPVNF ISAGLKKGAA EEAELEDSDD EEKPVKQDDF PKDFGPRKLK
121 TGGNFKPSQK GFAGGTKSFM DFGSWERHTK GIGQKLLQKM GYVPGRGLGK NAQGIINPIE
181 AKQRKGKGAV GAYGSERTTQ SMQDFPVVDS EEEAEEEFQK ELSQWRKDPS GSKKKPKYSY
241 KTVEELKAKG RISKKLTAPQ KELSQVKVID MTGREQKVYY SYSQISHKHN VPDDGLPLQS
301 QQLPQSGKEA KAPGFALPEL EHNLQLLIDL TEQEIIQNDR QLQYERDMVV NLFHELEKMT
361 EVLDHEERVI SNLSKVLEMV EECERRMQPD CSNPLTLDEC ARIFETLQDK YYEEYRMSDR
421 VDLAVAIVYP LMKEYFKEWD PLKDCTYGTE IISKWKSLLE NDQLLSHGGQ DLSADAFHRL
481 IWEVWMPFVR NIVTQWQPRN CDPMVDFLDS WVHIIPVWIL DNILDQLIFP KLQKEVENWN
541 PLTDTVPIHS WIHPWLPLMQ ARLEPLYSPI RSKLSSALQK WHPSDSSAKL ILQPWKDVFT
601 PGSWEAFMVK NIVPKLGMCL GELVINPHQQ HMDAFYWVID WEGMISVSSL VGLLEKHFFP
661 KWLQVLCSWL SNSPNYEEIT KWYLGWKSMF SDQVLAHPSV KDKFNEALDI MNRAVSSNVG
721 AYMQPGAREN IAYLTHTERR KDFQYEAMQE RREAENMAQR GIGVAASSVP MNFKDLIETK
781 AEEHNIVFMP VIGKRHEGKQ LYTFGRIVIY IDRGVVFVQG EKTWVPTSLQ SLIDMAKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TFIP11 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)
- 0.43
- Highest tissue expression
- 59 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 59 nTPM
- skeletal muscle: 39 nTPM
- testis: 25 nTPM
- lymph node: 23 nTPM
- tonsil: 23 nTPM
- tongue: 20 nTPM
Single-cell type
- late primary spermatocytes: 107 nCPM
- early spermatids: 54 nCPM
- neutrophils: 40 nCPM
- syncytiotrophoblasts: 34 nCPM
- erythrocyte progenitors: 32 nCPM
- thymic myoid cells: 31 nCPM
Immune cell
- basophil: 69 nTPM
- eosinophil: 50 nTPM
- neutrophil: 45 nTPM
- T-reg: 45 nTPM
- non-classical monocyte: 44 nTPM
- naive B-cell: 43 nTPM
Brain region
- cerebellum: 34 nTPM
- cerebral cortex: 30 nTPM
- white matter: 30 nTPM
- basal ganglia: 30 nTPM
- thalamus: 29 nTPM
- hippocampal formation: 28 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about TFIP11.
Disease | ImmuneIEDB
Conditions an epitope on TFIP11 was assayed in.
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)
- 0.83
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.35
- DepMap mean gene effect
- -1.09
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- biomineral tissue development
- mRNA splicing, via spliceosome
- negative regulation of double-strand break repair via nonhomologous end joining
- negative regulation of protein-containing complex assembly
- protection from non-homologous end joining at telomere
- RNA processing
- spliceosomal complex disassembly
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- G-patch domain
- GCF, C-terminal
- G-patch domain
- GC-rich sequence DNA-binding factor-like protein
- Tuftelin interacting protein, N-terminal domain
- Septin and tuftelin interacting protein
- TFP11/STIP/Ntr1
- Tuftelin interacting protein N terminal
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TFIP11 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 TFIP11 as an antibody target. Whether an autoantibody or antibody against TFIP11 could matter depends on whether native TFIP11 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TFIP11 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 TFIP11 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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