Lifespan changes: From wild type to clk-2;clk-3
18
22.3
49.66%
Double mutant clk-2(qm37);clk-3(qm38) has a lifespan of 22.3 days, while single mutant clk-2(qm37) has a lifespan of 18.7 days, single mutant clk-3(qm38) has a lifespan of 20.4 days and wild type has a lifespan of 14.9 days.
Almost additive (positive)
Lakowski B, Hekimi S, 1996, Determination of life-span in Caenorhabditis elegans by four clock genes. Science. 272(5264):1010-3 8638122 Click here to select all mutants from this PubMed ID in the graph
20
20.6
27.95%
Double mutant clk-2(qm37);clk-3(qm38) has a lifespan of 20.6 days, while single mutant clk-2(qm37) has a lifespan of 18.0 days, single mutant clk-3(qm38) has a lifespan of 19.9 days and wild type has a lifespan of 16.1 days.
Almost additive (positive)
Lakowski B, Hekimi S, 1996, Determination of life-span in Caenorhabditis elegans by four clock genes. Science. 272(5264):1010-3 8638122 Click here to select all mutants from this PubMed ID in the graph
15
33.8
Double mutant clk-2(qm37);clk-3(qm38) has a lifespan of 33.8 days, while single mutant clk-2(qm37) has a lifespan of 24.6 days and single mutant clk-3(qm38) has a lifespan of 25.7 days.
Partially known monotony. Positive epistasis
Lakowski B, Hekimi S, 1996, Determination of life-span in Caenorhabditis elegans by four clock genes. Science. 272(5264):1010-3 8638122 Click here to select all mutants from this PubMed ID in the graph
Telomere length regulation protein clk-2
Locus: CELE_C07H6.6
Wormbase description: The clk-2 gene encodes an ortholog of the S. cerevisiae telomere length-regulating protein Tel2p that has been shown to bind a number of DNA structures in vitro, including single-, double- and four-stranded DNA; in C. elegans, CLK-2 activity is required for the DNA damage and S phase replication checkpoints, for embryonic development, and for normal biological rhythms and life span; a functional CLK-2::GFP fusion protein is detected exclusively in the cytoplasm of somatic tissues.
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SynergyAge database hosts high-quality, manually curated information about the synergistic and antagonistic lifespan effects of genetic interventions in model organisms, also allowing users to explore the longevity relationships between genes in a visual way.
If you would like to cite this database please use:
Bunu, G., Toren, D., Ion, C. et al. SynergyAge, a curated database for synergistic and antagonistic interactions of longevity-associated genes. Sci Data 7, 366 (2020). https://doi.org/10.1038/s41597-020-00710-z
Group webpage: www.aging-research.group