ANAPC15
Anaphase-promoting complex subunit 15
Also known as: APC15, APC15_HUMAN, C11orf51, DKFZP564M082, HSPC020
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P60006
- Gene
- ANAPC15
- Ensembl
- ENSG00000110200
- Chromosome
- 11
- Canonical length
- 121 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Vesicles
OverviewNCBI Gene
Involved in anaphase-promoting complex-dependent catabolic process; protein polyubiquitination; and regulation of mitotic cell cycle spindle assembly checkpoint. Part of anaphase-promoting complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
121 residues, UniProt reviewed canonical sequence.
>P60006|ANAPC15
1 MSTLFPSLFP RVTETLWFNL DRPCVEETEL QQQEQQHQAW LQSIAEKDNN LVPIGKPASE
61 HYDDEEEEDD EDDEDSEEDS EDDEDMQDMD EMNDYNESPD DGEVNEVDME GNEQDQDQWM
121 ILocalizationUniProt · AlphaFold · HPA
Whether an antibody against ANAPC15 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)
- 0.65
- Highest tissue expression
- 94 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 94 nTPM
- skeletal muscle: 93 nTPM
- amygdala: 87 nTPM
- cerebral cortex: 83 nTPM
- basal ganglia: 83 nTPM
- midbrain: 77 nTPM
Single-cell type
- esophageal basal cells: 143 nCPM
- early primary spermatocytes: 138 nCPM
- undifferentiated spermatogonia: 128 nCPM
- differentiating spermatogonia: 124 nCPM
- esophageal suprabasal cells: 113 nCPM
- hofbauer cells: 104 nCPM
Immune cell
- classical monocyte: 174 nTPM
- T-reg: 158 nTPM
- myeloid DC: 154 nTPM
- eosinophil: 141 nTPM
- total PBMC: 128 nTPM
- plasmacytoid DC: 123 nTPM
Brain region
- cerebral cortex: 44 nTPM
- hypothalamus: 43 nTPM
- white matter: 42 nTPM
- basal ganglia: 41 nTPM
- midbrain: 41 nTPM
- spinal cord: 40 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)
- 0.78
- gnomAD pLI
- 0.3
- gnomAD missense Z
- 1.22
- DepMap mean gene effect
- -0.59
- DepMap dependency class
- common
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
- anaphase-promoting complex-dependent catabolic process
- cell division
- protein branched polyubiquitination
- protein K11-linked ubiquitination
- protein K48-linked ubiquitination
- regulation of meiotic cell cycle
- regulation of mitotic cell cycle
- regulation of mitotic cell cycle spindle assembly checkpoint
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Anaphase-promoting complex subunit 15
- Anaphase-promoting complex subunit 15
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ANAPC15 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 ANAPC15 as an antibody target. Whether an autoantibody or antibody against ANAPC15 could matter depends on whether native ANAPC15 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ANAPC15 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 ANAPC15 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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