Cone-rod dystrophy 1 - progressive retinal atrophy (crd4/cord1-PRA)

Order number: GSD361
€48.79

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Application: - Identification of heterozygous carriers The test examines the mutation in the RPGRP1 gene, which was described in the original publication as a risk factor for cone-rod dystrophy 1-progressive retinal atrophy (crd4/cord1-PRA) in longhaired miniature dachshunds. Further research revealed that cord1 also occurs in other breeds and is a multigenic disease in which the previously... more
Product information "Cone-rod dystrophy 1 - progressive retinal atrophy (crd4/cord1-PRA)"
Application:
- Identification of heterozygous carriers
The test examines the mutation in the RPGRP1 gene, which was described in the original publication as a risk factor for cone-rod dystrophy 1-progressive retinal atrophy (crd4/cord1-PRA) in longhaired miniature dachshunds. Further research revealed that cord1 also occurs in other breeds and is a multigenic disease in which the previously known mutations do not alone cause the impairment.
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Classification:
Type: DNA tests
Breeding clubs: Deutscher Teckelklub 1888 e.V., DTK
Class: Inherited diseases
Species: Dog
Breed: Kaninchenteckel Kurzhaar, Kaninchenteckel Langhaar, Kaninchenteckel Rauhaar, Mischling Hund, Teckel, Teckel Kurzhaar, Teckel Langhaar, Teckel Rauhaar, unbekannt, Zwergteckel Kurzhaar, Zwergteckel Langhaar, Zwergteckel Rauhaar
Group: Eyes
Test bundle 1 for wire-haired Dachshunds
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Test bundle 1 Coat Characteristics Dachshund.
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Hereditary diseases Dachshund - Bundle 1
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A – Locus / Agouti - DOG
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Centronuclear Myopathy (CNM)
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crd-PRA
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Curly Coat
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D – Locus (Dilution)
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Glykogen storage disease GSDIIIa
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Harlequin coat pattern
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L – Locus (hair length)
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Malignant Hyperthermia - DOG
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Von-Willebrand-Disease Type 1
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Cystinuria-A (Newfoundland)
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Juvenile Myoclonic Epilepsy
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IVDD-Type 1
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prcd-PRA***
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HNPK
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Exercise Induced Collapse (EIC)***
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STGD - Stargardt Disease
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Hämophilie B [p]
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Malignant Hyperthermia - HORSE
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Polysaccharide Storage Myopathy 1 (PSSM1***)
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DNA profile Identity DOG (ISAG-22-Marker)
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Neuronal Ceroid Lipofuscinosis 10 (NCL10)
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Griscelli Type 1 like syndrome
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Hyperkalemic Periodic Paralysis (HYPP)
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Junctional Epidermolysis Bullosa (JEB)
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Generalized Progressive Retinal Atrophy (gPRA)
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Cone-rod dystrophy 1 (crd-1)
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