PRA rdyProgressive Retinal Atrophy

44,90

Specific to Abyssin, Somali breeds

Gwaje-gwaje turnaround : 3-6 kwanaki ko Express 3 days
breeds : Abyssin, Somali
samfurori : Buccal swab, ko Blood a EDTA tube, ko Blood a bushe tube

Clear
SKU: pra-rdy-progressive-retinal-atrophy-abyssin-somali category:
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.

Fahimtar sakamakon gwajin: 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 sunan: PRA rdy - Progressive Retinal Atrophy
Gene maye gurbi: CRX n.546delC
gadar hali: autosomal rinjaye (ƙarin bayani)
Penetrance: cikakken (ƙarin bayani)
Test sakamakonPRA rdy - Progressive Retinal Atrophy matsayi (CRX n.546delC)Health matsayi
N/NNo copy of the PRA rdy mutationAnimal ne al'ada (bayyanannu)
PRA rdy/N1 copy of the PRA rdy mutationAnimal ne, zai ko za a iya shafa
PRA rdy/PRA rdy2 copies of the PRA rdy mutationAnimal ne, zai ko za a iya shafa

Cross tebur na gwajin: PRA rdy - Progressive Retinal Atrophy


uwar N/Nuwar PRA rdy/Nuwar PRA rdy/PRA rdy
Uba N/N100% N/N50% N/N
50% PRA rdy/N
100% PRA rdy/N
Uba 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
Uba PRA rdy/PRA rdy100% PRA rdy/N50% PRA rdy/N
50% PRA rdy/PRA rdy
100% PRA rdy/PRA rdy

Certificate misali ga gwajin: PRA rdy - Progressive Retinal Atrophy

Click a kan misali takardar shaidar kasa bude shi.

Certificate

References

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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