DCAF12
DDB1- and CUL4-associated factor 12
Also known as: CT102, DCA12_HUMAN, DKFZP434O125, KIAA1892, MGC1058, TCC52, WDR40A
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5T6F0
- Gene
- DCAF12
- Ensembl
- ENSG00000198876
- Chromosome
- 9
- Canonical length
- 453 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
This gene encodes a WD repeat-containing protein that interacts with the COP9 signalosome, a macromolecular complex that interacts with cullin-RING E3 ligases and regulates their activity by hydrolyzing cullin-Nedd8 conjugates. [provided by RefSeq, Jul 2009]
Canonical amino-acid sequenceUniProt
453 residues, UniProt reviewed canonical sequence.
>Q5T6F0|DCAF12
1 MARKVVSRKR KAPASPGAGS DAQGPQFGWD HSLHKRKRLP PVKRSLVYYL KNREVRLQNE
61 TSYSRVLHGY AAQQLPSLLK EREFHLGTLN KVFASQWLNH RQVVCGTKCN TLFVVDVQTS
121 QITKIPILKD REPGGVTQQG CGIHAIELNP SRTLLATGGD NPNSLAIYRL PTLDPVCVGD
181 DGHKDWIFSI AWISDTMAVS GSRDGSMGLW EVTDDVLTKS DARHNVSRVP VYAHITHKAL
241 KDIPKEDTNP DNCKVRALAF NNKNKELGAV SLDGYFHLWK AENTLSKLLS TKLPYCRENV
301 CLAYGSEWSV YAVGSQAHVS FLDPRQPSYN VKSVCSRERG SGIRSVSFYE HIITVGTGQG
361 SLLFYDIRAQ RFLEERLSAC YGSKPRLAGE NLKLTTGKGW LNHDETWRNY FSDIDFFPNA
421 VYTHCYDSSG TKLFVAGGPL PSGLHGNYAG LWSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DCAF12 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)
- 0.3
- Highest tissue expression
- 58 nTPM
Expression across tissuesHPA
Tissue
- testis: 58 nTPM
- tonsil: 40 nTPM
- lymph node: 35 nTPM
- bone marrow: 32 nTPM
- adrenal gland: 31 nTPM
- esophagus: 29 nTPM
Single-cell type
- erythrocytes: 402 nCPM
- esophageal apical cells: 267 nCPM
- early spermatids: 174 nCPM
- kupffer cells: 129 nCPM
- late primary spermatocytes: 125 nCPM
- neutrophil progenitors: 75 nCPM
Immune cell
- basophil: 37 nTPM
- classical monocyte: 29 nTPM
- eosinophil: 28 nTPM
- neutrophil: 28 nTPM
- myeloid DC: 25 nTPM
- intermediate monocyte: 24 nTPM
Brain region
- choroid plexus: 23 nTPM
- medulla oblongata: 19 nTPM
- white matter: 17 nTPM
- spinal cord: 17 nTPM
- midbrain: 17 nTPM
- pons: 17 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about DCAF12.
Disease | ImmuneIEDB
Conditions an epitope on DCAF12 was assayed in.
- colorectal cancer T cell
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)
- 0.86
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.55
- DepMap mean gene effect
- -0.08
- DepMap dependency class
- selective
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
- protein ubiquitination
- regulation of autophagy
- T cell activation
- ubiquitin-dependent protein catabolic process via the C-end degron rule pathway
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of DCAF12 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 DCAF12 as an antibody target. Whether an autoantibody or antibody against DCAF12 could matter depends on whether native DCAF12 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DCAF12 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 DCAF12 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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