IMPACT
Protein IMPACT
Also known as: IMPCT_HUMAN, RWDD5
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9P2X3
- Gene
- IMPACT
- Ensembl
- ENSG00000154059
- Chromosome
- 18
- Canonical length
- 320 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Predicted to enable protein sequestering activity. Predicted to be involved in several processes, including GCN2-mediated signaling; cellular response to amino acid starvation; and regulation of gene expression. Predicted to act upstream of or within negative regulation of protein phosphorylation. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
320 residues, UniProt reviewed canonical sequence.
>Q9P2X3|IMPACT
1 MAEGDAGSDQ RQNEEIEAMA AIYGEEWCVI DDCAKIFCIR ISDDIDDPKW TLCLQVMLPN
61 EYPGTAPPIY QLNAPWLKGQ ERADLSNSLE EIYIQNIGES ILYLWVEKIR DVLIQKSQMT
121 EPGPDVKKKT EEEDVECEDD LILACQPESS LKALDFDISE TRTEVEVEEL PPIDHGIPIT
181 DRRSTFQAHL APVVCPKQVK MVLSKLYENK KIASATHNIY AYRIYCEDKQ TFLQDCEDDG
241 ETAAGGRLLH LMEILNVKNV MVVVSRWYGG ILLGPDRFKH INNCARNILV EKNYTNSPEE
301 SSKALGKNKK VRKDKKRNEHLocalizationUniProt · AlphaFold · HPA
Whether an antibody against IMPACT 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)
- 0.37
- Highest tissue expression
- 32 nTPM
Expression across tissuesHPA
Tissue
- testis: 32 nTPM
- thyroid gland: 30 nTPM
- parathyroid gland: 26 nTPM
- breast: 24 nTPM
- salivary gland: 24 nTPM
- kidney: 23 nTPM
Single-cell type
- early primary spermatocytes: 96 nCPM
- differentiating spermatogonia: 71 nCPM
- undifferentiated spermatogonia: 66 nCPM
- breast lactating cells: 62 nCPM
- megakaryocytes: 56 nCPM
- late primary spermatocytes: 54 nCPM
Immune cell
- basophil: 66 nTPM
- eosinophil: 19 nTPM
- intermediate monocyte: 12 nTPM
- myeloid DC: 12 nTPM
- classical monocyte: 9.6 nTPM
- non-classical monocyte: 9.1 nTPM
Brain region
- hypothalamus: 41 nTPM
- midbrain: 27 nTPM
- medulla oblongata: 22 nTPM
- white matter: 22 nTPM
- spinal cord: 22 nTPM
- pons: 22 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)
- 1.12
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.17
- DepMap mean gene effect
- 0.08
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cellular response to amino acid starvation
- GCN2-mediated signaling
- intracellular signal transduction
- negative regulation of transcription by RNA polymerase II
- neuron projection extension
- positive regulation of neuron differentiation
- regulation of translational initiation
- regulation of cytoplasmic translational initiation in response to stress
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- RWD domain
- Ubiquitin-conjugating enzyme/RWD-like
- Ribosomal protein uS5 domain 2-type superfamily
- RWD domain
- Impact, N-terminal
- Uncharacterised protein family UPF0029, Impact, conserved site
- Impact family
- Impact, N-terminal domain superfamily
- Impact N-terminal domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of IMPACT 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 IMPACT as an antibody target. Whether an autoantibody or antibody against IMPACT could matter depends on whether native IMPACT is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
IMPACT 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 IMPACT as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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