Seroatlas · Human Serome Atlas

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 VRKDKKRNEH

LocalizationUniProt · 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

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

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.

Canonical record: https://seroatlas.com/gene/IMPACT. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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