OMIA:002455-9031 : Fragile X syndrome, FMR1-related in Gallus gallus (chicken) |
In other species: white-tufted-ear marmoset
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: unknown
Considered a defect: yes
Genetic engineering:
Unknown
Have human generated variants been created, e.g. through genetic engineering and gene editing
Cite this entry
Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2023). OMIA:002455-9031: 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. | |
| 2020 | Wang, X., Kohl, A., Yu, X., Zorio, D.A.R., Klar, A., Sela-Donenfeld, D., Wang, Y. : |
| Temporal-specific roles of fragile X mental retardation protein in the development of the hindbrain auditory circuit. Development 147:dev188797, 2020. Pubmed reference: 32747436. DOI: 10.1242/dev.188797. |
Edit History
- Created by Imke Tammen2 on 17 Jan 2023
- Changed by Imke Tammen2 on 16 Oct 2023