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


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