PRA rdyProgressive Retinal Atrophy

44,90

Specific to Abyssin, Somali breeds

Tes perputaran : 3-6 hari atau Express 3 hari
Breeds : Abyssin, Somali
Sampel : Buccal Swab, atau darah dalam tabung EDTA, atau darah dalam tabung kering

Jelas
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.

Memahami hasil tes: 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.
Nama uji: PRA rdy - Progressive Retinal Atrophy
Mutasi gen: CRX n.546delC
Keturunan: autosomal dominant (informasi lebih lanjut)
Penetrance : complete (informasi lebih lanjut)
Hasil tesPRA rdy - Progressive Retinal Atrophy statusCRX n.546delC)Status kesehatan
N/NNo copy of the PRA rdy mutationHewan adalah normal (jelas)
PRA rdy/N1 copy of the PRA rdy mutationHewan adalah, akan atau dapat dipengaruhi
PRA rdy/PRA rdy2 copies of the PRA rdy mutationHewan adalah, akan atau dapat dipengaruhi

Cross Table dari tes: PRA rdy - Progressive Retinal Atrophy


Ibu N/NIbu PRA rdy/NIbu PRA rdy/PRA rdy
Bapa N/N100% N/N50% N/N
50% PRA rdy/N
100% PRA rdy/N
Bapa 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
Bapa PRA rdy/PRA rdy100% PRA rdy/N50% PRA rdy/N
50% PRA rdy/PRA rdy
100% PRA rdy/PRA rdy

Sertifikat contoh tes: PRA rdy - Progressive Retinal Atrophy

Klik pada sertifikat contoh di bawah ini untuk membukanya.

Sertifikat

Referensi

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.

Ulasan

Ada tidak ada ulasan belum.

Hanya Login Pelanggan yang telah membeli produk ini dapat meninggalkan review.