- German Shorthaired Pointer
- CNGB3
- Organes sensoriels
Achromatopsia 3 (Day Blindness) – Pointer type
€57,48 €47,50 excl. BTW
Description
Achromatopsia (sometimes referred to as Cone Degeneration or Hemeralopia) is an eye disorder that can cause day blindness, sensitivity to light and a loss of colour vision. This particular form of the disorder is known as Achromatopsia-3, and is caused by a recessive mutation to the gene CNGB3. The variant analysed in this test occurs in the German Shorthaired Pointer. A related variant has been found in the Alaskan Malamute, Siberian Husky and Australian Shepherd.
Informations complémentaires
| Breeds | |
|---|---|
| Gene | |
| Organ | |
| specimen | Swab, Blood EDTA, Blood Heparin, Semen, Tissue, Swab, Blood EDTA, Blood Heparin, Semen, Tissue |
| Mode of Inheritance | |
| Chromosome | |
| Also known as | |
| Year Published |
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