OMIA:002455-9483 : Fragile X syndrome, FMR1-related in Callithrix jacchus (white-tufted-ear marmoset)

In other species: chicken

Categories: Nervous system phene

Links to possible relevant human trait(s) and/or gene(s) in OMIM: 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).

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
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].


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
  • Changed by Imke Tammen2 on 10 Dec 2023