OMIA:002158-9541 : Developmental retardation in Macaca fascicularis (crab-eating macaque) |
Categories: Mortality / aging (incl. embryonic lethal)
Links to possible relevant human trait(s) and/or gene(s) in OMIM: 606211 (gene)
Mendelian trait/disorder: yes
Disease-related: yes
Key variant known: yes
Year key variant first reported: 2018
Species-specific description: This is genetically-modified organism (GMO)
Molecular basis: Zhang et al. (2018) generated "a SIRT6-null cynomolgus monkey (Macaca fascicularis) model using a CRISPR-Cas9-based approach. SIRT6-deficient monkeys die hours after birth and exhibit severe prenatal developmental retardation".
Genetic engineering:
Yes - variants have been created artificially, e.g. by genetic engineering or gene editing
Have human generated variants been created, e.g. through genetic engineering and gene editing
Associated gene:
Symbol | Description | Species | Chr | Location | OMIA gene details page | Other Links |
---|---|---|---|---|---|---|
SIRT6 | sirtuin 6 | Macaca fascicularis | 19 | NC_088393.1 (4921755..4912514) | SIRT6 | Homologene, Ensembl , NCBI gene |
Cite this entry
Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2023). OMIA:002158-9541: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
Reference
2018 | Zhang, W., Wan, H., Feng, G., Qu, J., Wang, J., Jing, Y., Ren, R., Liu, Z., Zhang, L., Chen, Z., Wang, S., Zhao, Y., Wang, Z., Yuan, Y., Zhou, Q., Li, W., Liu, G.H., Hu, B. : |
SIRT6 deficiency results in developmental retardation in cynomolgus monkeys. Nature 560:661-665, 2018. Pubmed reference: 30135584. DOI: 10.1038/s41586-018-0437-z. |
Edit History
- Created by Frank Nicholas on 03 Sep 2018
- Changed by Imke Tammen2 on 10 Dec 2023