FREY1
Protein Frey 1
Also known as: C11orf94, Frey, FREY_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- C9JXX5
- Gene
- FREY1
- Ensembl
- ENSG00000234776
- Chromosome
- 11
- Canonical length
- 98 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
Predicted to enable protein-macromolecule adaptor activity. Predicted to be involved in fusion of sperm to egg plasma membrane involved in single fertilization; maintenance of protein localization in endoplasmic reticulum; and sperm-egg recognition. Predicted to act upstream of or within several processes, including protein modification process; protein stabilization; and spermatid development. Predicted to be located in endoplasmic reticulum. Predicted to be active in endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
98 residues, UniProt reviewed canonical sequence.
>C9JXX5|FREY1
1 MVLAMLGALH PRAGLSLFLH LILAVALLRS QPLRSQRSVP EAFSAPLELS QPLSGLVDDY
61 GILPKHPRPR GPRPLLSRAQ QRKRDGPDLA EYYYDAHLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against FREY1 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.59
- Highest tissue expression
- 55 nTPM
Expression across tissuesHPA
Tissue
- testis: 55 nTPM
- esophagus: 0.3 nTPM
- adipose tissue: 0 nTPM
- adrenal gland: 0 nTPM
- amygdala: 0 nTPM
- appendix: 0 nTPM
Single-cell type
- early spermatids: 436 nCPM
- late spermatids: 264 nCPM
- late primary spermatocytes: 198 nCPM
- cone photoreceptor cells: 2.1 nCPM
- sertoli cells: 2 nCPM
- peritubular myoid cells: 1.2 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
- choroid plexus: 0.3 nTPM
- cerebral cortex: 0.1 nTPM
- medulla oblongata: 0.1 nTPM
- amygdala: 0 nTPM
- basal ganglia: 0 nTPM
- cerebellum: 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)
- 1.74
- gnomAD pLI
- 0.04
- DepMap mean gene effect
- -0.02
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- fusion of sperm to egg plasma membrane involved in single fertilization
- gene expression
- intracellular calcium ion homeostasis
- maintenance of protein localization in endoplasmic reticulum
- protein localization involved in acrosome reaction
- protein N-linked glycosylation
- protein stabilization
- protein ubiquitination
- protein-containing complex assembly
- sperm-egg recognition
- spermatid development
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Protein Frey
- Protein Frey
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of FREY1 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 FREY1 as an antibody target. Whether an autoantibody or antibody against FREY1 could matter depends on whether native FREY1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
FREY1 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 FREY1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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