PRA rdyProgressive Retinal Atrophy

44,90

Specific to Abyssin, Somali breeds

Testleri gerçekleştirme : 3-6 gün veya Ekspres 3 gün
Doğur -mak : Abyssin, Somali
Örnekleri : Buccal bez, veya EDTA tüpünde Kan veya kuru tüpkan

Açık
SKU: pra-rdy-progressive-retinal-atrophy-abyssin-somali Kategori:
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.

Test sonuçlarının anlaşılması: 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.
Test adı : PRA rdy - Progressive Retinal Atrophy
Gen Mutasyonu : CRX n.546delC
Kalıtım: autosomal dominant (daha fazla bilgi)
Penetrance : complete (daha fazla bilgi)
Test sonucuPRA rdy - Progressive Retinal Atrophy durumu (CRX n.546delC)Sağlık durumu
N/NNo copy of the PRA rdy mutationHayvan normaldir (açık)
PRA rdy/N1 copy of the PRA rdy mutationHayvan, olacak ya da etkilenebilir
PRA rdy/PRA rdy2 copies of the PRA rdy mutationHayvan, olacak ya da etkilenebilir

Testin çapraz tablosu: PRA rdy - Progressive Retinal Atrophy


Anne N/NAnne PRA rdy/NAnne PRA rdy/PRA rdy
Baba N/N100% N/N50% N/N
50% PRA rdy/N
100% PRA rdy/N
Baba 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
Baba PRA rdy/PRA rdy100% PRA rdy/N50% PRA rdy/N
50% PRA rdy/PRA rdy
100% PRA rdy/PRA rdy

Test için sertifika örneği: PRA rdy - Progressive Retinal Atrophy

Açmak için aşağıdaki örnek sertifikaya tıklayın.

Sertifika

Referanslar

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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