Seroatlas · Human Serome Atlas

FRAT2

GSK-3-binding protein FRAT2

Also known as: FRAT2_HUMAN

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
O75474
Gene
FRAT2
Ensembl
ENSG00000181274
Chromosome
10
Canonical length
233 aa
Protein class
Predicted intracellular proteins
Subcellular location
Nucleoplasm,Mitochondria

OverviewNCBI Gene

The protein encoded by this intronless gene belongs to the GSK-3-binding protein family. Studies show that this protein plays a role as a positive regulator of the WNT signaling pathway. It may be upregulated in tumor progression. [provided by RefSeq, Jul 2008]

Canonical amino-acid sequenceUniProt

233 residues, UniProt reviewed canonical sequence.

>O75474|FRAT2
     1  MPCRREEEEE AGEEAEGEEE EDDSFLLLQQ SVTLGSSGEV DRLVAQIGET LQLDAAQDSP
    61  ASPCAPPGVP LRAPGPLAAA VPADKARPPA VPLLLPPASA ETVGPAPSGA LRCALGDRGR
   121  VRGRAAPYCV AEVAAGPSAL PGPCRRGWLR DAVTSRRLQQ RRWTQAGARA GDDDPHRLLQ
   181  QLVLSGNLIK EAVRRLQRAV AAVAATGPAS APGPGGGRSG PDRIALQPSG SLL

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against FRAT2 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)
0.68
Highest tissue expression
29 nTPM

Expression across tissuesHPA

Tissue

  • bone marrow: 29 nTPM
  • spleen: 27 nTPM
  • duodenum: 24 nTPM
  • skin: 20 nTPM
  • liver: 18 nTPM
  • colon: 16 nTPM

Single-cell type

  • neutrophils: 286 nCPM
  • neutrophil progenitors: 77 nCPM
  • late spermatids: 65 nCPM
  • endometrial luminal cells: 64 nCPM
  • breast lactating cells: 49 nCPM
  • early spermatids: 46 nCPM

Immune cell

  • neutrophil: 58 nTPM
  • eosinophil: 15 nTPM
  • basophil: 8.3 nTPM
  • non-classical monocyte: 7.9 nTPM
  • classical monocyte: 7.2 nTPM
  • intermediate monocyte: 4.8 nTPM

Brain region

  • choroid plexus: 15 nTPM
  • medulla oblongata: 11 nTPM
  • cerebellum: 11 nTPM
  • midbrain: 11 nTPM
  • thalamus: 10 nTPM
  • cerebral cortex: 10 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)
1.69
gnomAD pLI
0.05
gnomAD missense Z
0.41
DepMap mean gene effect
-0.15
DepMap dependency class
selective

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).

OntologyGO

Biological processes

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads FRAT2 as an antibody target. Whether an autoantibody or antibody against FRAT2 could matter depends on whether native FRAT2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

FRAT2 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 FRAT2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/FRAT2. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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