DEDD2
DNA-binding death effector domain-containing protein 2
Also known as: DEDD2_HUMAN, FLAME-3
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8WXF8
- Gene
- DEDD2
- Ensembl
- ENSG00000160570
- Chromosome
- 19
- Canonical length
- 326 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes a nuclear-localized protein containing a death effector domain (DED). The encoded protein may regulate the trafficking of caspases and other proteins into the nucleus during death receptor-induced apoptosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012]
Canonical amino-acid sequenceUniProt
326 residues, UniProt reviewed canonical sequence.
>Q8WXF8|DEDD2
1 MALSGSTPAP CWEEDECLDY YGMLSLHRMF EVVGGQLTEC ELELLAFLLD EAPGAAGGLA
61 RARSGLELLL ELERRGQCDE SNLRLLGQLL RVLARHDLLP HLARKRRRPV SPERYSYGTS
121 SSSKRTEGSC RRRRQSSSSA NSQQGQWETG SPPTKRQRRS RGRPSGGARR RRRGAPAAPQ
181 QQSEPARPSS EGKVTCDIRL RVRAEYCEHG PALEQGVASR RPQALARQLD VFGQATAVLR
241 SRDLGSVVCD IKFSELSYLD AFWGDYLSGA LLQALRGVFL TEALREAVGR EAVRLLVSVD
301 EADYEAGRRR LLLMEEEGGR RPTEASLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DEDD2 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)
- 0.48
- Highest tissue expression
- 22 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 22 nTPM
- pituitary gland: 20 nTPM
- spleen: 19 nTPM
- cerebral cortex: 17 nTPM
- hypothalamus: 16 nTPM
- lung: 14 nTPM
Single-cell type
- syncytiotrophoblasts: 211 nCPM
- neutrophils: 174 nCPM
- esophageal apical cells: 111 nCPM
- epididymal efferent duct absorptive cells: 75 nCPM
- colonocytes: 71 nCPM
- epididymal principal cells: 68 nCPM
Immune cell
- neutrophil: 127 nTPM
- eosinophil: 95 nTPM
- non-classical monocyte: 83 nTPM
- basophil: 82 nTPM
- intermediate monocyte: 73 nTPM
- total PBMC: 72 nTPM
Brain region
- hypothalamus: 44 nTPM
- cerebral cortex: 42 nTPM
- white matter: 42 nTPM
- pons: 39 nTPM
- thalamus: 32 nTPM
- midbrain: 32 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)
- 0.77
- gnomAD pLI
- 0.06
- gnomAD missense Z
- 1.34
- DepMap mean gene effect
- 0.06
- DepMap dependency class
- none
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
- apoptotic nuclear changes
- cellular homeostasis
- extrinsic apoptotic signaling pathway via death domain receptors
- intracellular signal transduction
- negative regulation of DNA-templated transcription
- positive regulation of extrinsic apoptotic signaling pathway
- RNA processing
- rRNA catabolic process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of DEDD2 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 DEDD2 as an antibody target. Whether an autoantibody or antibody against DEDD2 could matter depends on whether native DEDD2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DEDD2 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 DEDD2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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