PRA rdyProgressive Retinal Atrophy

44,90

Specific to Abyssin, Somali breeds

îmtîhan turnaround : 3-6 rojan an Express 3 rojan
Breeds : Abyssin, Somali
Samples : Bi paçekî buccal, an xwînê li tube EDTA, an xwînê li tube dry

Zelal
SKU: pra-rdy-progressive-retinal-atrophy-abyssin-somali Liq:
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.

Fêmkirina encamên testa: 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.
Navê Test: PRA rdy - Progressive Retinal Atrophy
Gene Mutation: CRX n.546delC
derbasdibe: autosomal serdest (Agahiyên zêdetir)
Penetrance: temam (Agahiyên zêdetir)
Di encama TestPRA rdy - Progressive Retinal Atrophy status (CRX n.546delC)rewşa tenduristiyê
N/NNo copy of the PRA rdy mutationAnimal normal e (zelal)
PRA rdy/N1 copy of the PRA rdy mutationAnimal e, yan jî dê nikare bê bandor
PRA rdy/PRA rdy2 copies of the PRA rdy mutationAnimal e, yan jî dê nikare bê bandor

table Cross ya test: PRA rdy - Progressive Retinal Atrophy


N/NPRA rdy/NPRA rdy/PRA rdy
Bav N/N100% N/N50% N/N
50% PRA rdy/N
100% PRA rdy/N
Bav 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
Bav PRA rdy/PRA rdy100% PRA rdy/N50% PRA rdy/N
50% PRA rdy/PRA rdy
100% PRA rdy/PRA rdy

nimûne sertîfîkayê ji bo testa: PRA rdy - Progressive Retinal Atrophy

li ser belgeya nimûne Click li jêr ji bo wan veke.

Şehade

Çavkanî

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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