DCUN1D3
DCN1-like protein 3
Also known as: DCNL3_HUMAN, DKFZp686O0290, FLJ41725, MGC48972, SCCRO3
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8IWE4
- Gene
- DCUN1D3
- Ensembl
- ENSG00000188215
- Chromosome
- 16
- Canonical length
- 304 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
Enables cullin family protein binding activity. Involved in several processes, including negative regulation of G1/S transition of mitotic cell cycle; regulation of protein neddylation; and response to UV-C. Located in several cellular components, including cytosol; nucleoplasm; and perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
304 residues, UniProt reviewed canonical sequence.
>Q8IWE4|DCUN1D3
1 MGQCVTKCKN PSSTLGSKNG DREPSNKSHS RRGAGHREEQ VPPCGKPGGD ILVNGTKKAE
61 AATEACQLPT SSGDAGRESK SNAEESSLQR LEELFRRYKD EREDAILEEG MERFCNDLCV
121 DPTEFRVLLL AWKFQAATMC KFTRKEFFDG CKAISADSID GICARFPSLL TEAKQEDKFK
181 DLYRFTFQFG LDSEEGQRSL HREIAIALWK LVFTQNNPPV LDQWLNFLTE NPSGIKGISR
241 DTWNMFLNFT QVIGPDLSNY SEDEAWPSLF DTFVEWEMER RKREGEGRGA LSSGPEGLCP
301 EEQTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DCUN1D3 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.4
- Highest tissue expression
- 27 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 27 nTPM
- adipose tissue: 19 nTPM
- retina: 12 nTPM
- liver: 11 nTPM
- blood vessel: 9.9 nTPM
- lung: 9.2 nTPM
Single-cell type
- paneth cells: 3.9 nCPM
- medullary thymic epithelial cells: 2.4 nCPM
- platelets: 1.4 nCPM
- urothelial cells: 1.4 nCPM
- ocular epithelial cells: 1.3 nCPM
- early spermatids: 1.2 nCPM
Immune cell
- basophil: 1.3 nTPM
- intermediate monocyte: 0.6 nTPM
- memory CD8 T-cell: 0.6 nTPM
- naive CD8 T-cell: 0.6 nTPM
- NK-cell: 0.6 nTPM
- non-classical monocyte: 0.5 nTPM
Brain region
- white matter: 19 nTPM
- cerebellum: 16 nTPM
- thalamus: 15 nTPM
- hypothalamus: 14 nTPM
- cerebral cortex: 14 nTPM
- midbrain: 13 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)
- 0.43
- gnomAD pLI
- 0.87
- gnomAD missense Z
- 1.4
- 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
- negative regulation of cell growth
- negative regulation of G1/S transition of mitotic cell cycle
- negative regulation of protein neddylation
- positive regulation of apoptotic process
- positive regulation of protein neddylation
- protein neddylation
- regulation of cell cycle process
- regulation of protein neddylation
- response to gamma radiation
- response to UV-C
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of DCUN1D3 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 DCUN1D3 as an antibody target. Whether an autoantibody or antibody against DCUN1D3 could matter depends on whether native DCUN1D3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DCUN1D3 is annotated at the cell surface, where native DCUN1D3 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label DCUN1D3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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