PRA rdyProgressive Retinal Atrophy

44,90

Specific to Abyssin, Somali breeds

Testu izpildes : 3-6 dienas vai izteikt 3 dienas
Šķirnes : Abyssin, Somali
Paraugu : Aiz vaiga lietojamās tamponu vai asinis EDTA caurulē, vai asinis sausā caurulē

Skaidrs
SKU: pra-rdy-progressive-retinal-atrophy-abyssin-somali Kategorija:
N/N : Normal, no copy of the PRA rdy mutation. N/PRA rdy : one copy of the PRA rdy mutation, the cat may develop this disease. PRA rdy/PRA rdy : 2 copies of the PRA rdy mutation, the cat may develop this disease.

What is PRA rdyProgressive Retinal Atrophy?

PRA rdyProgressive Retinal Atrophy is a specific mutation found in Abyssin and Somali cat. This disease produce rod cone dysplasia. Kittens will be blind at around 7 weeks old due to a defective protein which is needed for the normal eye development.

Izprast testa rezultātus: PRA rdy - Progressive Retinal Atrophy


N/N : Normal, no copy of the PRA rdy mutation. N/PRA rdy : one copy of the PRA rdy mutation, the cat may develop this disease. PRA rdy/PRA rdy : 2 copies of the PRA rdy mutation, the cat may develop this disease.
Testa nosaukums: PRA rdy - Progressive Retinal Atrophy
Gēnu mutācija: CRX n.546delC
Iedzimtību: autosomāli dominējošs (Papildinformācija)
Penetrance: complete (Papildinformācija)
Testa rezultātsPRA rdy - Progressive Retinal Atrophy statusuCRX n.546delC)Health status
N/NNo copy of the PRA rdy mutationAnimal is normal (clear)
PRA rdy/N1 copy of the PRA rdy mutationAnimal is, will or could be affected
PRA rdy/PRA rdy2 copies of the PRA rdy mutationAnimal is, will or could be affected

Testa Cross tabula: PRA rdy - Progressive Retinal Atrophy


Māte N/NMāte PRA rdy/NMāte PRA rdy/PRA rdy
Tēvs N/N100% N/N50% N/N
50% PRA rdy/N
100% PRA rdy/N
Tēvs PRA rdy/N50% N/N
50% PRA rdy/N
25% N/N
50% PRA rdy/N
25% PRA rdy/PRA rdy
50% PRA rdy/N
50% PRA rdy/PRA rdy
Tēvs PRA rdy/PRA rdy100% PRA rdy/N50% PRA rdy/N
50% PRA rdy/PRA rdy
100% PRA rdy/PRA rdy

Pārbaudes sertifikāta piemērs: PRA rdy - Progressive Retinal Atrophy

Noklikšķiniet uz sertifikāta piemērs zemāk, lai to atvērtu.

Sertifikāts

Atsauces

Menotti-Raymond M, Deckman KH, David V, Myrkalo J, O’Brien SJ, Narfström K. Mutation discovered in a feline model of human congenital retinal blinding disease. Invest Ophthalmol Vis Sci. 2010 Jun; 51(6):2852-9. Epub 2010 Jan 6. PubMed PMID: 20053974.

Atsauksmes

Nav atsauksmes yet.

Tikai pieteicies klientiem, kuri ir iegādājušies šo produktu var atstāt atsauksmi.