GADD45G
Growth arrest and DNA damage-inducible protein GADD45 gamma
Also known as: CR6, DDIT2, GA45G_HUMAN, GADD45gamma, GRP17
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O95257
- Gene
- GADD45G
- Ensembl
- ENSG00000130222
- Chromosome
- 9
- Canonical length
- 159 aa
- Protein class
- Cancer-related genes, Plasma proteins, Predicted intracellular proteins
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene is a member of a group of genes whose transcript levels are increased following stressful growth arrest conditions and treatment with DNA-damaging agents. The protein encoded by this gene responds to environmental stresses by mediating activation of the p38/JNK pathway via MTK1/MEKK4 kinase. The GADD45G is highly expressed in placenta. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
159 residues, UniProt reviewed canonical sequence.
>O95257|GADD45G
1 MTLEEVRGQD TVPESTARMQ GAGKALHELL LSAQRQGCLT AGVYESAKVL NVDPDNVTFC
61 VLAAGEEDEG DIALQIHFTL IQAFCCENDI DIVRVGDVQR LAAIVGAGEE AGAPGDLHCI
121 LISNPNEDAW KDPALEKLSL FCEESRSVND WVPSITLPELocalizationUniProt · AlphaFold · HPA
Whether an antibody against GADD45G 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)
- 0.34
- Highest tissue expression
- 334 nTPM
Expression across tissuesHPA
Tissue
- liver: 334 nTPM
- heart muscle: 314 nTPM
- blood vessel: 215 nTPM
- adrenal gland: 143 nTPM
- skeletal muscle: 137 nTPM
- pituitary gland: 125 nTPM
Single-cell type
- syncytiotrophoblasts: 1,977 nCPM
- breast lactating cells: 468 nCPM
- decidual stromal cells: 291 nCPM
- epididymal principal cells: 281 nCPM
- respiratory ionocytes: 267 nCPM
- hepatocytes: 265 nCPM
Immune cell
- eosinophil: 4.9 nTPM
- neutrophil: 0.7 nTPM
- classical monocyte: 0.2 nTPM
- myeloid DC: 0.1 nTPM
- plasmacytoid DC: 0.1 nTPM
- basophil: 0 nTPM
Brain region
- cerebellum: 40 nTPM
- cerebral cortex: 29 nTPM
- basal ganglia: 27 nTPM
- hypothalamus: 22 nTPM
- thalamus: 21 nTPM
- midbrain: 17 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)
- 0.72
- gnomAD pLI
- 0.55
- gnomAD missense Z
- 2
- DepMap mean gene effect
- -0.04
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- apoptotic process
- cell differentiation
- positive regulation of apoptotic process
- positive regulation of cold-induced thermogenesis
- positive regulation of JNK cascade
- positive regulation of p38MAPK cascade
- regulation of cell cycle
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of GADD45G 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 GADD45G as an antibody target. Whether an autoantibody or antibody against GADD45G could matter depends on whether native GADD45G is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GADD45G 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 GADD45G as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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