DDIT4
DNA damage-inducible transcript 4 protein
Also known as: DDIT4_HUMAN, Dig2, FLJ20500, REDD-1, REDD1, RTP801
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NX09
- Gene
- DDIT4
- Ensembl
- ENSG00000168209
- Chromosome
- 10
- Canonical length
- 232 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
Predicted to enable 14-3-3 protein binding activity. Involved in negative regulation of TOR signaling and response to hypoxia. Located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
232 residues, UniProt reviewed canonical sequence.
>Q9NX09|DDIT4
1 MPSLWDRFSS SSTSSSPSSL PRTPTPDRPP RSAWGSATRE EGFDRSTSLE SSDCESLDSS
61 NSGFGPEEDT AYLDGVSLPD FELLSDPEDE HLCANLMQLL QESLAQARLG SRRPARLLMP
121 SQLVSQVGKE LLRLAYSEPC GLRGALLDVC VEQGKSCHSV GQLALDPSLV PTFQLTLVLR
181 LDSRLWPKIQ GLFSSANSPF LPGFSQSLTL STGFRVIKKK LYSSEQLLIE ECLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DDIT4 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)
- 0.46
- Highest tissue expression
- 596 nTPM
Expression across tissuesHPA
Tissue
- ovary: 596 nTPM
- pancreas: 480 nTPM
- vagina: 455 nTPM
- blood vessel: 393 nTPM
- cervix: 376 nTPM
- esophagus: 316 nTPM
Single-cell type
- esophageal apical cells: 4,027 nCPM
- esophageal suprabasal cells: 1,522 nCPM
- prostatic hillock cells: 1,046 nCPM
- basal prostatic cells: 903 nCPM
- pancreatic acinar cells: 805 nCPM
- breast lactating cells: 801 nCPM
Immune cell
- NK-cell: 409 nTPM
- naive CD4 T-cell: 275 nTPM
- MAIT T-cell: 250 nTPM
- gdT-cell: 237 nTPM
- total PBMC: 215 nTPM
- naive CD8 T-cell: 214 nTPM
Brain region
- choroid plexus: 82 nTPM
- medulla oblongata: 80 nTPM
- white matter: 66 nTPM
- thalamus: 65 nTPM
- midbrain: 57 nTPM
- cerebellum: 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)
- 1.28
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.1
- 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
- apoptotic process
- brain development
- cellular response to dexamethasone stimulus
- defense response to virus
- intracellular signal transduction
- intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator
- negative regulation of glycolytic process
- negative regulation of TOR signaling
- neuron differentiation
- neuron migration
- neurotrophin TRK receptor signaling pathway
- protein-containing complex disassembly
- reactive oxygen species metabolic process
- response to hypoxia
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of DDIT4 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 DDIT4 as an antibody target. Whether an autoantibody or antibody against DDIT4 could matter depends on whether native DDIT4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DDIT4 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 DDIT4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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