NCL 5 Neuronal ceroid lipofuscinosisGolden Retrievers

64,90

Specific to the Golden Retrievers

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

清楚
Sku: ncl-5-neuronal-ceroid-lipofuscinosis-golden-retrievers 类别:
N/N : Normal, no copies of the NCL5 mutation. N/NCL5 : Normal, one copy of the NCL5 mutation. NCL5/NCL5 : 2 copies of the NCL5 mutation, the dog may develop this disease.

What is the NCL 5 Neuronal ceroid lipofuscinosis in the Golden Retrievers ?

The clinical signs of NCL in the Golden Retriever is progressive neurological disorders such as a disorientation, an anxiety, a dog that becomes aggressive, a dog that has problems with food intake. We can also observe a loss of vision. The first signs arrive at the age of 15 months.

样品类型

下面是此测试接受的不同类型的示例的列表:
  • 布卡尔斯瓦布
  • EDTA 管中的血液
  • 干管中的血液

可用于测试的品种 : NCL 5 Neuronal ceroid lipofuscinosis - Golden Retrievers


以下品种被识别:
  • Golden Retriever

了解测试结果 : NCL 5 Neuronal ceroid lipofuscinosis - Golden Retrievers


N/N : Normal, no copies of the NCL5 mutation. N/NCL5 : Normal, one copy of the NCL5 mutation. NCL5/NCL5 : 2 copies of the NCL5 mutation, the dog may develop this disease.
测试名称 : NCL 5 Neuronal ceroid lipofuscinosis - Golden Retrievers
基因突变 : CLN5 c.934_935delAG
遗传: 常染色体隐性 (更多信息)
测试结果NCL 5 Neuronal ceroid lipofuscinosis - Golden Retrievers 状态(CLN5 c.934_935delAG)健康状况
N/NNo copy of the NCL5 mutation动物正常(透明)
N/NCL51 copy of the NCL5 mutation动物正常(透明)
NCL5/NCL52 copies of the NCL5 mutation动物是,将或可能受到影响

测试的交叉表 : NCL 5 Neuronal ceroid lipofuscinosis - Golden Retrievers


母亲 N/N母亲 N/NCL5母亲 NCL5/NCL5
父亲 N/N100% N/N50% N/N
50% N/NCL5
100% N/NCL5
父亲 N/NCL550% N/N
50% N/NCL5
25% N/N
50% N/NCL5
25% NCL5/NCL5
50% N/NCL5
50% NCL5/NCL5
父亲 NCL5/NCL5100% N/NCL550% N/NCL5
50% NCL5/NCL5
100% NCL5/NCL5

测试的证书示例: NCL 5 Neuronal ceroid lipofuscinosis - Golden Retrievers

单击下面的示例证书以将其打开。

证书

引用

Gilliam, D., Kolicheski, A., Johnson, G.S., Mhlanga-Mutangadura, T., Taylor, J.F., Schnabel, R.D., Katz, M.L. : Golden Retriever dogs with neuronal ceroid lipofuscinosis have a two-base-pair deletion and frameshift in CLN5. Mol Genet Metab 115:101-9, 2015

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