FRAT1
Proto-oncogene FRAT1
Also known as: FRAT1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q92837
- Gene
- FRAT1
- Ensembl
- ENSG00000165879
- Chromosome
- 10
- Canonical length
- 279 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Vesicles,Cytosol
OverviewNCBI Gene
The protein encoded by this gene belongs to the GSK-3-binding protein family. The protein inhibits GSK-3-mediated phosphorylation of beta-catenin and positively regulates the Wnt signaling pathway. It may function in tumor progression and in lymphomagenesis. [provided by RefSeq, Oct 2008]
Canonical amino-acid sequenceUniProt
279 residues, UniProt reviewed canonical sequence.
>Q92837|FRAT1
1 MPCRREEEEE AGEEAEGEEE EEDSFLLLQQ SVALGSSGEV DRLVAQIGET LQLDAAQHSP
61 ASPCGPPGAP LRAPGPLAAA VPADKARSPA VPLLLPPALA ETVGPAPPGV LRCALGDRGR
121 VRGRAAPYCV AELATGPSAL SPLPPQADLD GPPGAGKQGI PQPLSGPCRR GWLRGAAASR
181 RLQQRRGSQP ETRTGDDDPH RLLQQLVLSG NLIKEAVRRL HSRRLQLRAK LPQRPLLGPL
241 SAPVHEPPSP RSPRAACSDP GASGRAQLRT GDGVLVPGSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against FRAT1 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)
- 0.7
- Highest tissue expression
- 12 nTPM
Expression across tissuesHPA
Tissue
- spleen: 12 nTPM
- liver: 12 nTPM
- testis: 11 nTPM
- bone marrow: 10 nTPM
- appendix: 4.7 nTPM
- stomach: 4.5 nTPM
Single-cell type
- late spermatids: 135 nCPM
- neutrophils: 91 nCPM
- early spermatids: 38 nCPM
- neutrophil progenitors: 32 nCPM
- megakaryocytes: 31 nCPM
- monocytes: 30 nCPM
Immune cell
- neutrophil: 10 nTPM
- eosinophil: 8.7 nTPM
- classical monocyte: 2 nTPM
- non-classical monocyte: 1.5 nTPM
- intermediate monocyte: 1.3 nTPM
- myeloid DC: 1 nTPM
Brain region
- hypothalamus: 7.6 nTPM
- cerebellum: 7.5 nTPM
- medulla oblongata: 7.1 nTPM
- cerebral cortex: 6.9 nTPM
- midbrain: 6.8 nTPM
- pons: 6 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)
- 1.11
- gnomAD pLI
- 0.32
- gnomAD missense Z
- 0.23
- DepMap mean gene effect
- -0.03
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- canonical Wnt signaling pathway
- positive regulation of canonical Wnt signaling pathway
- regulation of protein export from nucleus
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of FRAT1 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 FRAT1 as an antibody target. Whether an autoantibody or antibody against FRAT1 could matter depends on whether native FRAT1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
FRAT1 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 FRAT1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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