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CHEK2
CHEK2
<div class="infobox infobox-gene">
<span class="infobox-title">CHEK2</span>
<table>
<tr><th>Full Name</th><td>Checkpoint Kinase 2</td></tr>
<tr><th>Chromosomal Location</th><td>22q12.1</td></tr>
<tr><th>NCBI Gene ID</th><td>1111</td></tr>
<tr><th>OMIM</th><td>604373</td></tr>
<tr><th>Ensembl ID</th><td>ENSG00000149554</td></tr>
<tr><th>UniProt ID</th><td>O96017</td></tr>
<tr><th>Protein</th><td>CHEK2 protein</td></tr>
<tr><th>Associated Diseases</th><td>Li-Fraumeni syndrome variant, Prostate cancer, Breast cancer, Osteosarcoma, Glioma</td></tr>
</table>
</div>
Overview
...
CHEK2
<div class="infobox infobox-gene">
<span class="infobox-title">CHEK2</span>
<table>
<tr><th>Full Name</th><td>Checkpoint Kinase 2</td></tr>
<tr><th>Chromosomal Location</th><td>22q12.1</td></tr>
<tr><th>NCBI Gene ID</th><td>1111</td></tr>
<tr><th>OMIM</th><td>604373</td></tr>
<tr><th>Ensembl ID</th><td>ENSG00000149554</td></tr>
<tr><th>UniProt ID</th><td>O96017</td></tr>
<tr><th>Protein</th><td>CHEK2 protein</td></tr>
<tr><th>Associated Diseases</th><td>Li-Fraumeni syndrome variant, Prostate cancer, Breast cancer, Osteosarcoma, Glioma</td></tr>
</table>
</div>
Overview
Checkpoint kinase 2 (CHEK2) is a serine/threonine-protein kinase encoded by the CHEK2 gene located on chromosome 22q12.1[@ahn2000]. CHEK2 plays a critical role in maintaining genomic stability through its involvement in the DNA damage checkpoint pathway. As a key effector of ATM-mediated DNA damage response, CHEK2 helps coordinate cell cycle arrest, DNA repair, and [apoptosis](/entities/apoptosis) in response to genotoxic stress["@matsuoka2000"].
Mutations in CHEK2 have been associated with increased cancer risk, particularly in the context of Li-Fraumeni-like syndromes. The protein's kinase activity is regulated by phosphorylation in response to DNA double-strand breaks, making it a potential therapeutic target in cancers with defective DNA repair mechanisms.
Function
<div class="infobox infobox-gene">
<span class="infobox-title">CHEK2</span>
<table>
<tr><th>Full Name</th><td>Checkpoint Kinase 2</td></tr>
<tr><th>Chromosomal Location</th><td>22q12.1</td></tr>
<tr><th>NCBI Gene ID</th><td>1111</td></tr>
<tr><th>OMIM</th><td>604373</td></tr>
<tr><th>Ensembl ID</th><td>ENSG00000149554</td></tr>
<tr><th>UniProt ID</th><td>O96017</td></tr>
<tr><th>Protein</th><td>CHEK2 protein</td></tr>
<tr><th>Associated Diseases</th><td>Li-Fraumeni syndrome variant, Prostate cancer, Breast cancer, Osteosarcoma, Glioma</td></tr>
</table>
</div>
Function
Checkpoint kinase 2 (CHEK2) is a serine/threonine-protein kinase that plays a critical role in the DNA damage checkpoint pathway[@ahn2000]. In response to DNA double-strand breaks (DSBs), ATM kinase phosphorylates CHEK2 at Thr68, activating its kinase activity[@matsuoka2000]. Activated CHEK2 then phosphorylates multiple downstream targets including:
- p53 (TP53): Phosphorylation at Ser20 disrupts MDM2-mediated degradation, stabilizing p53 and promoting DNA repair or apoptosis[@chehab2000]
- CDC25A/B/C: Phosphorylation leads to cell cycle arrest at G1/S and G2/M checkpoints[@zhou2004]
- BRCA1: Phosphorylation supports homologous recombination repair[@zhang2003]
- E2F1: Phosphorylation regulates transcription of pro-apoptotic genes[@stevens2003]
CHEK2 exists as a dimer that undergoes trans-autophosphorylation upon DNA damage[@cai2009]. The protein contains an N-terminal SQ/TQ cluster domain (SCD) with multiple ATM phosphorylation sites, a central forkhead-associated (FHA) domain, and a C-terminal kinase domain[@li2002].
Disease Associations
Cancer
- Li-Fraumeni syndrome: Heterozygous germline CHEK2*1100delC variant increases cancer risk 2-4 fold[@weischer2008]
- Prostate cancer: CHEK2 variants associated with aggressive disease[@seppala2003]
- Breast cancer: CHEK2 I157T variant increases risk 1.5-2 fold[@bane2007]
Neurodegeneration
- Alzheimer's disease: CHEK2 dysregulation reported in AD brain tissue; involved in neuronal DNA damage response[@hashimoto2002]
- [Parkinson's disease](/diseases/parkinsons-disease): CHEK2 phosphorylation patterns altered in PD models[@jhaveri2013]
- Amyotrophic lateral sclerosis (ALS): CHEK2 activation observed in ALS patient spinal cord[@sathasivam2014]
Expression
CHEK2 is ubiquitously expressed in human tissues with highest levels in testis, thymus, and prostate[@us]. In the brain, CHEK2 is expressed in:
- [Neurons](/entities/neurons) (cortical, hippocampal, cerebellar)[@inoue2002]
- [Astrocytes](/entities/astrocytes)
- [Microglia](/cell-types/microglia-neuroinflammation)
- [Oligodendrocytes](/cell-types/oligodendrocytes)
Expression increases in response to DNA damage, oxidative stress, and during aging[@rashielkeles2011].
Therapeutic Implications
- CHEK2 inhibitors: Preclinical compounds in development for cancer therapy[@antoni2007]
- DNA damage response modulators: Combination strategies with radiotherapy or chemotherapy[@zhou2014]
See Also
- [ATM](/genes/atm) - ATM kinase, upstream activator of CHEK2
- [p53](/mechanisms/p53-pathway) - Tumor suppressor, downstream target
- [DNA Damage Response](/mechanisms/dna-damage-response) - Broader pathway context
- [BRCA1](/genes/brca1) - DNA repair partner
- [Alzheimer's Disease](/diseases/alzheimers-disease) - Disease association
External Links
- [NCBI Gene: CHEK2](https://www.ncbi.nlm.nih.gov/gene/1111)
- [UniProt: O96017](https://www.uniprot.org/uniprot/O96017)
- [OMIM: 604373](https://www.omim.org/entry/604373)
References
Pathway Diagram
The following diagram shows the key molecular relationships involving CHEK2 discovered through SciDEX knowledge graph analysis:
▸Metadataorigin_type: v1_polymorphic_backfill
| slug | genes-check2 |
| kg_node_id | CHEK2 |
| entity_type | gene |
| origin_type | v1_polymorphic_backfill |
| source_table | wiki_pages |
| wiki_page_id | wp-e10da0c60dfa |
| __merged_from | {'merged_at': '2026-05-13', 'unprefixed_id': 'genes-check2'} |
| _schema_version | 1 |
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