PRA rdyProgressive Retinal Atrophy

44, 90

Specific to Abyssin, Somali breeds

Canvi de proves : dies 3-6 o expressar 3 dies
Races : Abyssin, Somali
Mostres : Swab bucal, o sang en tub EDTA o sang en tub sec

Clar
SKU: pra-rdy-progressive-retinal-atrophy-abyssin-somali Categoria:
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.

Resultats de comprensió de la prova: 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.
Nom de la prova: PRA rdy - Progressive Retinal Atrophy
Mutació genètica: CRX n.546delC
L'herència: autosomal dominant (més informació)
Penetrància complete (més informació)
Resultat de la provaPRA rdy - Progressive Retinal Atrophy (estatusCRX n.546delC)Estat de salut
N/NNo copy of the PRA rdy mutationAnimal és normal (clar)
PRA rdy/N1 copy of the PRA rdy mutationAnimal és, es o podria veure afectada
PRA rdy/PRA rdy2 copies of the PRA rdy mutationAnimal és, es o podria veure afectada

Creuar la taula de la prova: PRA rdy - Progressive Retinal Atrophy


Mare N/NMare PRA rdy/NMare PRA rdy/PRA rdy
Pare N/N100% N/N50% N/N
50% PRA rdy/N
100% PRA rdy/N
Pare 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
Pare PRA rdy/PRA rdy100% PRA rdy/N50% PRA rdy/N
50% PRA rdy/PRA rdy
100% PRA rdy/PRA rdy

Exemple de certificat de la prova: PRA rdy - Progressive Retinal Atrophy

Feu clic sobre el certificat d'exemple per sota per obrir-lo.

Certificat

Referències

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.

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