OMIA:002455-9483 : Fragile X syndrome, FMR1-related in Callithrix jacchus (white-tufted-ear marmoset) |
In other species: chicken
Categories: Nervous system phene
Possibly relevant human trait(s) and/or gene(s)s (MIM numbers): 300624 (trait) , 309550 (gene)
Links to MONDO diseases: No links.
Mendelian trait/disorder: yes
Considered a defect: yes
Key variant known: no
Species-specific description: This phene includes references to studies involving genetically modified organisms (GMO).
Genetic engineering:
Unknown
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 |
|---|---|---|---|---|---|---|
| FMR1 | fragile X mental retardation 1 | Callithrix jacchus | X | NC_071464.1 (139877912..139915845) | FMR1 | Homologene, Ensembl , NCBI gene |
Cite this entry
Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2023). OMIA:002455-9483: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
References
Note: the references are listed in reverse chronological order (from the most recent year to the earliest year), and alphabetically by first author within a year.
| 2022 | Curnow, E., Wang, Y. : |
| New animal models for understanding FMRP functions and FXS pathology. Cells 11:1628, 2022. Pubmed reference: 35626665. DOI: 10.3390/cells11101628. | |
| 2021 | Abe, Y., Nakao, H., Goto, M., Tamano, M., Koebis, M., Nakao, K., Aiba, A. : |
| Efficient marmoset genome engineering by autologous embryo transfer and CRISPR/Cas9 technology. Sci Rep 11:20234, 2021. Pubmed reference: 34642413. DOI: 10.1038/s41598-021-99656-4. |
Edit History
- Created by Imke Tammen2 on 19 Oct 2021
- Changed by Imke Tammen2 on 19 Oct 2021
- Changed by Imke Tammen2 on 17 Jan 2023