PRA rdyProgressive Retinal Atrophy

44,90

Specific to Abyssin, Somali breeds

测试周转 : 3-6 天或快递 3 天
品种 : Abyssin, Somali
样品 : 牛签拭子,或 EDTA 管中的血液,或干管中的血液

清楚
Sku: pra-rdy-progressive-retinal-atrophy-abyssin-somali 类别:
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.

了解测试结果 : 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.
测试名称 : PRA rdy - Progressive Retinal Atrophy
基因突变 : CRX n.546delC
遗传: autosomal dominant (更多信息)
佩内兰斯 : complete (更多信息)
测试结果PRA rdy - Progressive Retinal Atrophy 状态(CRX n.546delC)健康状况
N/NNo copy of the PRA rdy mutation动物正常(透明)
PRA rdy/N1 copy of the PRA rdy mutation动物是,将或可能受到影响
PRA rdy/PRA rdy2 copies of the PRA rdy mutation动物是,将或可能受到影响

测试的交叉表 : PRA rdy - Progressive Retinal Atrophy


母亲 N/N母亲 PRA rdy/N母亲 PRA rdy/PRA rdy
父亲 N/N100% N/N50% N/N
50% PRA rdy/N
100% PRA rdy/N
父亲 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
父亲 PRA rdy/PRA rdy100% PRA rdy/N50% PRA rdy/N
50% PRA rdy/PRA rdy
100% PRA rdy/PRA rdy

测试的证书示例: PRA rdy - Progressive Retinal Atrophy

单击下面的示例证书以将其打开。

证书

引用

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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