APOBEC3C
DNA dC->dU-editing enzyme APOBEC-3C
Also known as: ABC3C_HUMAN, APOBEC1L, ARDC2, ARDC4, ARP5, bK150C2.3, PBI
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NRW3
- Gene
- APOBEC3C
- Ensembl
- ENSG00000244509
- Chromosome
- 22
- Canonical length
- 190 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Subcellular location
- Intermediate filaments
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene is a member of the cytidine deaminase gene family. It is one of seven related genes or pseudogenes found in a cluster thought to result from gene duplication, on chromosome 22. Members of the cluster encode proteins that are structurally and functionally related to the C to U RNA-editing cytidine deaminase APOBEC1. It is thought that the proteins may be RNA editing enzymes and have roles in growth or cell cycle control. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
190 residues, UniProt reviewed canonical sequence.
>Q9NRW3|APOBEC3C
1 MNPQIRNPMK AMYPGTFYFQ FKNLWEANDR NETWLCFTVE GIKRRSVVSW KTGVFRNQVD
61 SETHCHAERC FLSWFCDDIL SPNTKYQVTW YTSWSPCPDC AGEVAEFLAR HSNVNLTIFT
121 ARLYYFQYPC YQEGLRSLSQ EGVAVEIMDY EDFKYCWENF VYNDNEPFKP WKGLKTNFRL
181 LKRRLRESLQLocalizationUniProt · AlphaFold · HPA
Whether an antibody against APOBEC3C 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)
- 0.27
- Highest tissue expression
- 63 nTPM
Expression across tissuesHPA
Tissue
- tonsil: 63 nTPM
- lymph node: 54 nTPM
- fallopian tube: 53 nTPM
- epididymis: 49 nTPM
- adrenal gland: 36 nTPM
- spleen: 34 nTPM
Single-cell type
- microglia: 9.3 nCPM
- erythrocyte progenitors: 6.5 nCPM
- platelets: 5.7 nCPM
- nk-cells: 5 nCPM
- megakaryocyte-erythroid progenitors: 4.7 nCPM
- oligodendrocyte progenitor cells: 3.9 nCPM
Immune cell
- gdT-cell: 309 nTPM
- eosinophil: 277 nTPM
- memory CD8 T-cell: 276 nTPM
- naive B-cell: 250 nTPM
- non-classical monocyte: 248 nTPM
- memory B-cell: 242 nTPM
Brain region
- white matter: 11 nTPM
- medulla oblongata: 7.9 nTPM
- spinal cord: 6.5 nTPM
- thalamus: 5.7 nTPM
- pons: 5.3 nTPM
- hypothalamus: 4.6 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)
- 0.94
- gnomAD pLI
- 0.03
- gnomAD missense Z
- -0.46
- DepMap mean gene effect
- -0.13
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- clearance of foreign intracellular DNA
- cytidine to uridine editing
- defense response to virus
- DNA cytosine deamination
- innate immune response
- negative regulation of single stranded viral RNA replication via double stranded DNA intermediate
- negative regulation of viral genome replication
- positive regulation of gene expression via chromosomal CpG island demethylation
- transposable element silencing
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of APOBEC3C 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 APOBEC3C as an antibody target. Whether an autoantibody or antibody against APOBEC3C could matter depends on whether native APOBEC3C is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
APOBEC3C 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 APOBEC3C as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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