CUEDC2
CUE domain-containing protein 2
Also known as: C10orf66, CUED2_HUMAN, MGC2491
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H467
- Gene
- CUEDC2
- Ensembl
- ENSG00000107874
- Chromosome
- 10
- Canonical length
- 287 aa
- Protein class
- Disease related genes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
Predicted to enable ubiquitin binding activity. Acts upstream of or within negative regulation of cytokine production involved in inflammatory response and negative regulation of macrophage cytokine production. Located in cytosol; nuclear membrane; and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
287 residues, UniProt reviewed canonical sequence.
>Q9H467|CUEDC2
1 MELERIVSAA LLAFVQTHLP EADLSGLDEV IFSYVLGVLE DLGPSGPSEE NFDMEAFTEM
61 MEAYVPGFAH IPRGTIGDMM QKLSGQLSDA RNKENLQPQS SGVQGQVPIS PEPLQRPEML
121 KEETRSSAAA AADTQDEATG AEEELLPGVD VLLEVFPTCS VEQAQWVLAK ARGDLEEAVQ
181 MLVEGKEEGP AAWEGPNQDL PRRLRGPQKD ELKSFILQKY MMVDSAEDQK IHRPMAPKEA
241 PKKLIRYIDN QVVSTKGERF KDVRNPEAEE MKATYINLKP ARKYRFHLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CUEDC2 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)
- 0.5
- Highest tissue expression
- 112 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 112 nTPM
- tongue: 111 nTPM
- choroid plexus: 101 nTPM
- heart muscle: 92 nTPM
- cerebral cortex: 88 nTPM
- amygdala: 85 nTPM
Single-cell type
- decidual stromal cells: 138 nCPM
- hofbauer cells: 95 nCPM
- epididymal principal cells: 88 nCPM
- schwann cells: 84 nCPM
- cytotrophoblasts: 83 nCPM
- esophageal basal cells: 82 nCPM
Immune cell
- myeloid DC: 112 nTPM
- classical monocyte: 112 nTPM
- basophil: 100 nTPM
- plasmacytoid DC: 98 nTPM
- NK-cell: 93 nTPM
- intermediate monocyte: 92 nTPM
Brain region
- cerebellum: 64 nTPM
- hypothalamus: 64 nTPM
- thalamus: 63 nTPM
- white matter: 58 nTPM
- pons: 57 nTPM
- basal ganglia: 56 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)
- 0.65
- gnomAD pLI
- 0.06
- gnomAD missense Z
- 1.38
- DepMap mean gene effect
- 0.12
- 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
- negative regulation of cytokine production involved in inflammatory response
- negative regulation of macrophage cytokine production
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Ubiquitin system component CUE
- CUE domain
- CUE domain-containing protein 2, CUE domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CUEDC2 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 CUEDC2 as an antibody target. Whether an autoantibody or antibody against CUEDC2 could matter depends on whether native CUEDC2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CUEDC2 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 CUEDC2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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