COIL
Coilin
Also known as: CLN80, COIL_HUMAN, p80-coilin
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P38432
- Gene
- COIL
- Ensembl
- ENSG00000121058
- Chromosome
- 17
- Canonical length
- 576 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nucleoli fibrillar center,Nuclear bodies
OverviewNCBI Gene
The protein encoded by this gene is an integral component of Cajal bodies (also called coiled bodies). Cajal bodies are nuclear suborganelles of varying number and composition that are involved in the post-transcriptional modification of small nuclear and small nucleolar RNAs. The N-terminus of the coilin protein directs its self-oligomerization while the C-terminus influences the number of nuclear bodies assembled per cell. Differential methylation and phosphorylation of coilin likely influences its localization among nuclear bodies and the composition and assembly of Cajal bodies. This gene has pseudogenes on chromosome 4 and chromosome 14. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
576 residues, UniProt reviewed canonical sequence.
>P38432|COIL
1 MAASETVRLR LQFDYPPPAT PHCTAFWLLV DLNRCRVVTD LISLIRQRFG FSSGAFLGLY
61 LEGGLLPPAE SARLVRDNDC LRVKLEERGV AENSVVISNG DINLSLRKAK KRAFQLEEGE
121 ETEPDCKYSK KHWKSRENNN NNEKVLDLEP KAVTDQTVSK KNKRKNKATC GTVGDDNEEA
181 KRKSPKKKEK CEYKKKAKNP KSPKVQAVKD WANQRCSSPK GSARNSLVKA KRKGSVSVCS
241 KESPSSSSES ESCDESISDG PSKVTLEARN SSEKLPTELS KEEPSTKNTT ADKLAIKLGF
301 SLTPSKGKTS GTTSSSSDSS AESDDQCLMS SSTPECAAGF LKTVGLFAGR GRPGPGLSSQ
361 TAGAAGWRRS GSNGGGQAPG ASPSVSLPAS LGRGWGREEN LFSWKGAKGR GMRGRGRGRG
421 HPVSCVVNRS TDNQRQQQLN DVVKNSSTII QNPVETPKKD YSLLPLLAAA PQVGEKIAFK
481 LLELTSSYSP DVSDYKEGRI LSHNPETQQV DIEILSSLPA LREPGKFDLV YHNENGAEVV
541 EYAVTQESKI TVFWKELIDP RLIIESPSNT SSTEPALocalizationUniProt · AlphaFold · HPA
Whether an antibody against COIL 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
- 92 nTPM
Expression across tissuesHPA
Tissue
- testis: 92 nTPM
- bone marrow: 19 nTPM
- tonsil: 13 nTPM
- thymus: 12 nTPM
- placenta: 12 nTPM
- liver: 12 nTPM
Single-cell type
- late spermatids: 905 nCPM
- late primary spermatocytes: 267 nCPM
- early spermatids: 224 nCPM
- oocytes: 124 nCPM
- early primary spermatocytes: 72 nCPM
- cytotrophoblasts: 53 nCPM
Immune cell
- memory B-cell: 28 nTPM
- naive B-cell: 25 nTPM
- basophil: 22 nTPM
- naive CD4 T-cell: 20 nTPM
- naive CD8 T-cell: 19 nTPM
- T-reg: 19 nTPM
Brain region
- cerebellum: 16 nTPM
- white matter: 12 nTPM
- cerebral cortex: 11 nTPM
- pons: 11 nTPM
- choroid plexus: 11 nTPM
- hypothalamus: 9.9 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about COIL.
Disease | ImmuneIEDB
Conditions an epitope on COIL was assayed in.
- systemic scleroderma B cell
ReferencesPubMed · IEDB
Publications for COIL from three distinct lines of evidence, kept separate because they answer different questions: whether antibodies are directed at the protein, whether a B-cell epitope has been mapped on it, and whether a T-cell epitope has. Each is labelled with its source.
Reference: AutoantibodyPubMed
5 publications
- Human autoantibody to a novel protein of the nuclear coiled body: immunological characterization and cDNA cloning of p80-coilin.
1991 · J Exp Med · RCR 6.4 · 330 citations - Anti-p80 coilin autoantibodies react with a conserved epitope and are associated with anti-DFS70/LEDGF autoantibodies.
2006 · J Autoimmun · RCR 0.6 · 22 citations - The behavior of the coiled body in cells infected with adenovirus in vitro.
1996 · Mol Biol Rep · RCR 0.4 · 20 citations - Clinical features and IgG subclass distribution of anti-p80 coilin antibodies.
1999 · J Autoimmun · RCR 0.3 · 10 citations - Distribution of anti-p80-coilin autoantibody in collagen diseases and various skin diseases.
1997 · Br J Dermatol · RCR 0.2 · 7 citations
Reference: B cellIEDB
1 publication
Sources: PubMed — antigen-level antibody evidence from a custom retrieval. Records matching a controlled set of autoantibody terms (the MeSH descriptors Autoantibodies and Autoantigens, with title and abstract term variants) were obtained through NCBI E-utilities, and their titles and abstracts parsed for constructions that direct an antibody at a named protein rather than for co-occurrence. Captured names were resolved against UniProt nomenclature and each antigen adjudicated individually against the source text. IEDB — curated epitope assays from the Immune Epitope Database (Vita et al., Nucleic Acids Research 2019). Bibliographic records from PubMed and MeSH, U.S. National Library of Medicine; citation metrics from NIH iCite (Hutchins et al., PLoS Biology 2016). Titles link to PubMed; abstracts are not reproduced here. The NLM does not endorse this analysis.
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)
- 0.59
- gnomAD pLI
- 0.01
- gnomAD missense Z
- 0.17
- DepMap mean gene effect
- -0.4
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 10% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Coilin
- Coilin, N-terminal domain
- Coilin, tudor domain
- Coilin N-terminus
- Coilin, C-terminal Tudor domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of COIL 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 COIL as an antibody target. Whether an autoantibody or antibody against COIL could matter depends on whether native COIL is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
COIL 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 COIL as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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