OMIA:002455-9031 : Fragile X syndrome, FMR1-related in Gallus gallus (chicken)

In other species: white-tufted-ear marmoset

Categories: Nervous system phene

Links to possible relevant human trait(s) and/or gene(s) in OMIM: 300624 (trait) , 309550 (gene)

Mendelian trait/disorder: unknown

Considered a defect: yes

Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2023). OMIA:002455-9031: 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.
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