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OMIA:001517-9615 : Retinal atrophy, progressive, X-linked, type 3 in Canis lupus familiaris (dog)

Categories: Vision / eye phene

Links to MONDO diseases: No links.

Mendelian trait/disorder: yes

Mode of inheritance: X-linked

Considered a defect: yes

Key variant known: no

Species-specific symbol: XLPRA3

Genetic engineering: Unknown
Have human generated variants been created, e.g. through genetic engineering and gene editing

Breed: Border Collie (Dog) (VBO_0200193).
Breeds in which the phene has been documented. For breeds in which a likely causal variant has been documented, see the variant table below

Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2023). OMIA:001517-9615: 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 Aguirre, G.D., Kazacos, K.R. :
Is it canine DUSN?: Another view of retinopathies, some acquired, and others possibly "inherited": Another view of retinopathies, some acquired, and others possibly "inherited". Vet Ophthalmol 25:96-108, 2022. Pubmed reference: 34894198. DOI: 10.1111/vop.12951.
2008 Vilboux, T., Chaudieu, G., Jeannin, P., Delattre, D., Hedan, B., Bourgain, C., Queney, G., Galibert, F., Thomas, A., André, C. :
Progressive retinal atrophy in the Border Collie: a new XLPRA. BMC Vet Res 4:10, 2008. Pubmed reference: 18315866. DOI: 10.1186/1746-6148-4-10.

Edit History


  • Created by Frank Nicholas on 02 Nov 2010
  • Changed by Imke Tammen2 on 16 Dec 2021
  • Changed by Imke Tammen2 on 17 Jun 2023