General description
enthält (15 Euro Patentgebühr für DM Exon2): Brachyurie (Stummelrute), Collie Eye Anomalie** (CEA) (Partnerlabor), Degenerative Myelopathie (DM Exon2), Hereditäre Katarakt (HSF4), MDR1-Gendefekt (Ivermectin-Überempfindlichkeit), Neuronale Ceroid Lipofuszinose (NCL) und Progressive Retinaatrophie*** (prcd-PRA) (Partnerlabor)
Australian Shepherd, Miniature American Shepherd
Order details
Test number | 8624 |
Sample material | 0,5 ml EDTA Blut, 2x Backenabstrich, 1x Spezialabstrich (eNAT) |
Test duration | 7-14 Werktage |
MDR1-Genvariante (Ivermectinunverträglichkeit)
Test specifications
Symptom complex | metabolisch |
Causality | ursächlich |
Gene | ABCB1 |
Mutation | DEL |
Literature | OMIA:001402-9615 |
Progressive Retinaatrophie (prcd-PRA)
Test specifications
Symptom complex | ophtalmisch |
Causality | ursächlich |
Gene | PRCD |
Mutation | C-T |
Literature | OMIA:001298-9615 |
Collie Eye Anomalie (CEA)
Test specifications
Symptom complex | ophtalmisch |
Age of onset | ab Geburt |
Causality | ursächlich |
Gene | NHEJ1 |
Mutation | COMPLEX |
Literature | OMIA:000218-9615 |
Hyperurikosurie (HUU/SLC)
Test specifications
Symptom complex | urologisch |
Causality | ursächlich |
Gene | SLC2A9 |
Mutation | G-T |
Literature | OMIA:001033-9615 |
Degenerative Myelopathie (DM) Exon 2
Test specifications
Symptom complex | neuromuskulär |
Age of onset | ab 8 Jahre |
Causality | Hochrisikofaktor |
Gene | SOD1 |
Mutation | G-A |
Literature | OMIA:000263-9615 |
Brachyurie (Stummelrute)
Test specifications
Symptom complex | skeletal |
Age of onset | ab Geburt |
Causality | ursächlich |
Gene | TBXT |
Mutation | G-C |
Literature | OMIA:000975-9615 |