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GeneQ14912280· pop 8· linked from 389 articles

Also known as CDS1, CHK2, HuCds1, LFS2, PP1425, RAD53, hCds1, checkpoint kinase 2

gen van de soort Homo sapiens

Gene data

CHEK2
Name
checkpoint kinase 2
Type
protein-coding
Position
28,687,738–28,742,422 (−)
Aliases
CDS1, CHK2, HuCds1, LFS2, PP1425, RAD53, TPDS4, hCds1
RefSeq RNA
NM_001005735.3, NM_001257387.3, NM_001349956.3, NM_001437942.1, NM_001438293.1
RefSeq protein
NP_001005735.1, NP_001244316.1, NP_001336885.1, NP_001424871.1, NP_001425222.1

In response to DNA damage and replication blocks, cell cycle progression is halted through the control of critical cell cycle regulators. The protein encoded by this gene is a cell cycle checkpoint regulator and putative tumor suppressor. It contains a forkhead-associated protein interaction domain essential for activation in response to DNA damage and is rapidly phosphorylated in response to replication blocks and DNA damage. When activated, the encoded protein is known to inhibit CDC25C phosphatase, preventing entry into mitosis, and has been shown to stabilize the tumor suppressor protein p53, leading to cell cycle arrest in G1. In addition, this protein interacts with and phosphorylates BRCA1, allowing BRCA1 to restore survival after DNA damage. Mutations in this gene have been linked with Li-Fraumeni syndrome, a highly penetrant familial cancer phenotype usually associated with inherited mutations in TP53. Also, mutations in this gene are thought to confer a predisposition to sarcomas, breast cancer, and brain tumors. This nuclear protein is a member of the CDS1 subfamily of serine/threonine protein kinases. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012].

via MyGene.info

Gene · Ensembl

checkpoint kinase 2

Symbol
CHEK2
Biotype
Protein coding
Organism
Homo sapiens
Location
22:28,687,738-28,742,422
Strand
Reverse (−)
Assembly
GRCh38
View on Ensembl →

via Ensembl · EMBL-EBI

Wikidata facts

Instance of
gene
Image
Protein CHEK2 PDB 1gxc.png
Show 8 more facts
HomoloGene ID
38289
genetic association
urogenital neoplasm
genomic start
29083731
found in taxon
Homo sapiens
genomic end
29138410
cytogenetic location
22q12.1
Sources (6)

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