CYREN
Cell cycle regulator of non-homologous end joining
Also known as: C7orf49, CYREN_HUMAN, FLJ22450, FLJ27285, MGC5242, MRI, MRI-2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BWK5
- Gene
- CYREN
- Ensembl
- ENSG00000122783
- Chromosome
- 7
- Canonical length
- 157 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
Predicted to enable molecular adaptor activity. Involved in double-strand break repair via nonhomologous end joining and negative regulation of double-strand break repair via nonhomologous end joining. Located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
157 residues, UniProt reviewed canonical sequence.
>Q9BWK5|CYREN
1 METLQSETKT RVLPSWLTAQ VATKNVAPMK APKRMRMAAV PVAAARLPAT RTVYCMNEAE
61 IVDVALGILI ESRKQEKACE QPALAGADNP EHSPPCSVSP HTSSGSSSEE EDSGKQALAP
121 GLSPSQRPGG SSSACSRSPE EEEEEDVLKY VREIFFSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CYREN 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)
- 0.66
- Highest tissue expression
- 33 nTPM
Expression across tissuesHPA
Tissue
- choroid plexus: 33 nTPM
- skeletal muscle: 32 nTPM
- kidney: 29 nTPM
- parathyroid gland: 25 nTPM
- tonsil: 22 nTPM
- seminal vesicle: 22 nTPM
Single-cell type
- cardiomyocytes: 196 nCPM
- platelets: 160 nCPM
- adipocytes: 107 nCPM
- endometrial luminal cells: 104 nCPM
- myonuclei: 97 nCPM
- endometrial glandular cells: 94 nCPM
Immune cell
- basophil: 32 nTPM
- myeloid DC: 30 nTPM
- eosinophil: 28 nTPM
- classical monocyte: 28 nTPM
- NK-cell: 27 nTPM
- plasmacytoid DC: 26 nTPM
Brain region
- medulla oblongata: 33 nTPM
- choroid plexus: 33 nTPM
- white matter: 31 nTPM
- basal ganglia: 25 nTPM
- pons: 24 nTPM
- cerebellum: 24 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)
- 1.31
- gnomAD pLI
- 0.26
- DepMap mean gene effect
- 0.03
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 12% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- double-strand break repair via nonhomologous end joining
- immunoglobulin V(D)J recombination
- negative regulation of double-strand break repair via nonhomologous end joining
- positive regulation of double-strand break repair via nonhomologous end joining
- protein localization to site of double-strand break
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Modulator of retrovirus infection
- Modulator of retrovirus infection
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CYREN 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 CYREN as an antibody target. Whether an autoantibody or antibody against CYREN could matter depends on whether native CYREN is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CYREN 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 CYREN as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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