SPINDOC
Spindlin interactor and repressor of chromatin-binding protein
Also known as: C11orf84, SPIN-DOC, SPNDC_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BUA3
- Gene
- SPINDOC
- Ensembl
- ENSG00000168005
- Chromosome
- 11
- Canonical length
- 381 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nuclear speckles
OverviewNCBI Gene
Involved in DNA damage response and negative regulation of DNA-templated transcription. Is active in nucleus and site of DNA damage. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
381 residues, UniProt reviewed canonical sequence.
>Q9BUA3|SPINDOC
1 MALKAEGAAL DCFEVTLKCE EGEDEEEAMV VAVIPRPEPM LRVTQQEKTP PPRPSPLEAG
61 SDGCEEPKQQ VSWEQEFLVG SSPGGSGRAL CMVCGAEIRA PSADTARSHI LEQHPHTLDL
121 SPSEKSNILE AWSEGVALLQ DVRAEQPSPP NSDSGQDAHP DPDANPDAAR MPAEIVVLLD
181 SEDNPSLPKR SRPRGLRPLE LPAVPATEPG NKKPRGQRWK EPPGEEPVRK KRGRPMTKNL
241 DPDPEPPSPD SPTETFAAPA EVRHFTDGSF PAGFVLQLFS HTQLRGPDSK DSPKDREVAE
301 GGLPRAESPS PAPPPGLRGT LDLQVIRVRM EEPPAVSLLQ DWSRHPQGTK RVGAGDTSDW
361 PTVLSESSTT VAGKPEKGNG VLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SPINDOC 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)
- 0.62
- Highest tissue expression
- 38 nTPM
Expression across tissuesHPA
Tissue
- testis: 38 nTPM
- placenta: 25 nTPM
- cerebellum: 19 nTPM
- colon: 19 nTPM
- endometrium: 18 nTPM
- prostate: 18 nTPM
Single-cell type
- tuft cells: 35 nCPM
- cytotrophoblasts: 28 nCPM
- breast myoepithelial cells: 24 nCPM
- megakaryocyte progenitors: 22 nCPM
- innate lymphoid cells: 21 nCPM
- endometrial secretory cells: 17 nCPM
Immune cell
- basophil: 0.5 nTPM
- gdT-cell: 0.3 nTPM
- naive B-cell: 0.3 nTPM
- plasmacytoid DC: 0.3 nTPM
- memory B-cell: 0.2 nTPM
- memory CD8 T-cell: 0.1 nTPM
Brain region
- hypothalamus: 45 nTPM
- cerebral cortex: 38 nTPM
- pons: 38 nTPM
- cerebellum: 37 nTPM
- midbrain: 35 nTPM
- basal ganglia: 33 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)
- 0.21
- gnomAD pLI
- 0.99
- DepMap mean gene effect
- -0.07
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- DNA damage response
- negative regulation of DNA-templated transcription
- regulation of protein ADP-ribosylation
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SPINDOC 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 SPINDOC as an antibody target. Whether an autoantibody or antibody against SPINDOC could matter depends on whether native SPINDOC is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SPINDOC 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 SPINDOC as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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