ANAPC13
Anaphase-promoting complex subunit 13
Also known as: APC13, APC13_HUMAN, DKFZP566D193, SWM1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BS18
- Gene
- ANAPC13
- Ensembl
- ENSG00000129055
- Chromosome
- 3
- Canonical length
- 74 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Mitochondria,Cytosol
OverviewNCBI Gene
This gene encodes a component of the anaphase promoting complex, a large ubiquitin-protein ligase that controls cell cycle progression by regulating the degradation of cell cycle regulators such as B-type cyclins. The encoded protein is evolutionarily conserved and is required for the integrity and ubiquitin ligase activity of the anaphase promoting complex. Pseudogenes and splice variants have been found for this gene; however, the biological validity of some of the splice variants has not been determined. [provided by RefSeq, Nov 2008]
Canonical amino-acid sequenceUniProt
74 residues, UniProt reviewed canonical sequence.
>Q9BS18|ANAPC13
1 MDSEVQRDGR ILDLIDDAWR EDKLPYEDVA IPLNELPEPE QDNGGTTESV KEQEMKWTDL
61 ALQYLHENVP PIGNLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ANAPC13 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)
- 0.6
- Highest tissue expression
- 113 nTPM
Expression across tissuesHPA
Tissue
- kidney: 113 nTPM
- epididymis: 108 nTPM
- choroid plexus: 108 nTPM
- heart muscle: 92 nTPM
- thyroid gland: 89 nTPM
- skeletal muscle: 86 nTPM
Single-cell type
- parietal cells: 279 nCPM
- gastric chief cells: 208 nCPM
- oocytes: 198 nCPM
- late spermatids: 145 nCPM
- decidual stromal cells: 132 nCPM
- epididymal principal cells: 131 nCPM
Immune cell
- neutrophil: 229 nTPM
- non-classical monocyte: 111 nTPM
- basophil: 111 nTPM
- intermediate monocyte: 108 nTPM
- classical monocyte: 96 nTPM
- naive CD4 T-cell: 94 nTPM
Brain region
- choroid plexus: 76 nTPM
- hypothalamus: 52 nTPM
- pons: 49 nTPM
- medulla oblongata: 44 nTPM
- midbrain: 41 nTPM
- white matter: 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)
- 1.86
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.13
- DepMap mean gene effect
- -0.52
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% 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
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Apc13
- Apc13p protein
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ANAPC13 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 ANAPC13 as an antibody target. Whether an autoantibody or antibody against ANAPC13 could matter depends on whether native ANAPC13 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ANAPC13 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 ANAPC13 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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