CIR1
Corepressor interacting with RBPJ 1
Also known as: CIR, CIR1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q86X95
- Gene
- CIR1
- Ensembl
- ENSG00000138433
- Chromosome
- 2
- Canonical length
- 450 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nuclear speckles
OverviewNCBI Gene
Enables histone deacetylase binding activity; protein kinase binding activity; and transcription corepressor activity. Acts upstream of or within negative regulation of transcription by RNA polymerase II. Located in centrosome and nuclear speck. Part of protein-containing complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
450 residues, UniProt reviewed canonical sequence.
>Q86X95|CIR1
1 MGKSFANFMC KKDFHPASKS NIKKVWMAEQ KISYDKKKQE ELMQQYLKEQ ESYDNRLLMG
61 DERVKNGLNF MYEAPPGAKK ENKEKEETEG ETEYKFEWQK GAPREKYAKD DMNIRDQPFG
121 IQVRNVRCIK CHKWGHVNTD RECPLFGLSG INASSVPTDG SGPSMHPSEL IAEMRNSGFA
181 LKRNVLGRNL TANDPSQEYV ASEGEEDPEV EFLKSLTTKQ KQKLLRKLDR LEKKKKKKDR
241 KKKKFQKSRS KHKKHKSSSS SSSSSSSSSS TETSESSSES ESNNKEKKIQ RKKRKKNKCS
301 GHNNSDSEEK DKSKKRKLHE ELSSSHHNRE KAKEKPRFLK HESSREDSKW SHSDSDKKSR
361 THKHSPEKRG SERKEGSSRS HGREERSRRS RSRSPGSYKQ RETRKRAQRN PGEEQSRRND
421 SRSHGTDLYR GEKMYREHPG GTHTKVTQRELocalizationUniProt · AlphaFold · HPA
Whether an antibody against CIR1 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)
- 0.61
- Highest tissue expression
- 66 nTPM
Expression across tissuesHPA
Tissue
- choroid plexus: 66 nTPM
- bone marrow: 63 nTPM
- epididymis: 41 nTPM
- ovary: 34 nTPM
- breast: 34 nTPM
- spleen: 33 nTPM
Single-cell type
- neutrophils: 584 nCPM
- oocytes: 580 nCPM
- late primary spermatocytes: 560 nCPM
- fallopian tube ciliated cells: 286 nCPM
- endometrial ciliated cells: 266 nCPM
- respiratory ciliated cells: 237 nCPM
Immune cell
- neutrophil: 188 nTPM
- basophil: 71 nTPM
- eosinophil: 56 nTPM
- NK-cell: 46 nTPM
- memory B-cell: 41 nTPM
- naive B-cell: 41 nTPM
Brain region
- white matter: 33 nTPM
- choroid plexus: 33 nTPM
- cerebral cortex: 33 nTPM
- cerebellum: 30 nTPM
- basal ganglia: 30 nTPM
- hypothalamus: 28 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)
- 0.99
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.04
- DepMap mean gene effect
- -0.39
- DepMap dependency class
- selective
OntologyGO
Biological processes
- in utero embryonic development
- mRNA processing
- negative regulation of DNA-templated transcription
- negative regulation of transcription by RNA polymerase II
- RNA splicing
Molecular functions
- histone deacetylase binding
- protein kinase binding
- protein-containing complex binding
- transcription corepressor activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- CBF1-interacting co-repressor CIR, N-terminal domain
- N-terminal domain of CBF1 interacting co-repressor CIR
- Corepressor interacting with RBPJ 1
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CIR1 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 CIR1 as an antibody target. Whether an autoantibody or antibody against CIR1 could matter depends on whether native CIR1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CIR1 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 CIR1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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