OMIA 002455-9483 : Fragile X syndrome, FMR1-related in Callithrix jacchus |
Possibly relevant human trait(s) and/or gene(s)s (MIM numbers):
300624 (trait)
,
309550 (gene)
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).
Associated gene:
| Symbol | Description | Species | Chr | Location | OMIA gene details page | Other Links |
|---|---|---|---|---|---|---|
| FMR1 | fragile X mental retardation 1 | Callithrix jacchus | X | NC_048405.1 (141110301..141148302) | FMR1 | Homologene, Ensembl, NCBI gene |
Reference
| 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