Varaico: Literature-Extracted Genetic Variants

Gene:CHEK1
Variant:p.D130A
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CHEK1

NM_001114122.3:p.D130A

Associated Papers

Discriminating activating, deactivating and resistance variants in protein kinases.

Singh G et al.

Genome Medicine, 2025

41152984 (PubMed )
Supplement: 13073_2025_1564_MOESM2_ESM.xlsx › Table_S5

Nuclear ATR lysine-tyrosylation protects against heart failure by activating DNA damage response.

Zhao R et al.

Cell Reports, 2023

Small molecule inhibitors and a kinase-dead expressing mouse model demonstrate that the kinase activity of Chk1 is essential for mouse embryos and cancer cells.

Muralidharan SV et al.

Life Science Alliance, 2020

32571801 (PubMed )
Supplement: LSA-2020-00671_review_history.pdf

SPRTN protease and checkpoint kinase 1 cross-activation loop safeguards DNA replication.

Halder S et al.

Nature Communications, 2019

31316063 (PubMed )
Supplement: 41467_2019_11095_MOESM1_ESM.pdf

Mitotic arrest by tumor suppressor RASSF1A is regulated via CHK1 phosphorylation.

Jiang L et al.

Molecular Cancer Research : Mcr, 2014

Candidate tumor suppressor BTG3 maintains genomic stability by promoting Lys63-linked ubiquitination and activation of the checkpoint kinase CHK1.

Cheng YC et al.

Proceedings of the National Academy of Sciences of the United States of America, 2013

DNA damage-induced CHK1 autophosphorylation at Ser296 is regulated by an intramolecular mechanism.

Okita N et al.

Febs Letters, 2012

DNA damage induces Chk1-dependent centrosome amplification.

Bourke E et al.

Embo Reports, 2007

The relative contribution of CHK1 and CHK2 to Adriamycin-induced checkpoint.

Ho CC et al.

Experimental Cell Research, 2005

Regulatory interactions between the checkpoint kinase Chk1 and the proteins of the DNA-dependent protein kinase complex.

Goudelock DM et al.

The Journal of Biological Chemistry, 2003

Ataxia-telangiectasia-mutated (ATM) and NBS1-dependent phosphorylation of Chk1 on Ser-317 in response to ionizing radiation.

Gatei M et al.

The Journal of Biological Chemistry, 2003

Determination of substrate motifs for human Chk1 and hCds1/Chk2 by the oriented peptide library approach.

O'Neill T et al.

The Journal of Biological Chemistry, 2002

The human homologs of checkpoint kinases Chk1 and Cds1 (Chk2) phosphorylate p53 at multiple DNA damage-inducible sites.

Shieh SY et al.

Genes & Development, 2000

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."