General description
includes: Degenerative myelopathy (exon 2), Hyperurikosuria (SLC) and Juvenile laryngeal paralysis & polyneuropathy (JLPP
Russian Black Terrier
Order details
Test number | 8756 |
Sample material | 0.5 ml EDTA blood, 2x cheek swab, 1x special swab (eNAT) |
Test duration | 3-5 working days |
Hyperuricosuria (HUU/SLC)
Test specifications
Symptom complex | urological |
Inheritance | autosomal recessive |
Causality | causally |
Gene | SLC2A9 |
Mutation | G-T |
Literature | OMIA:001033-9615 |
Degenerative myelopathy exon 2 (DM exon 2)
Test specifications
Symptom complex | neuromuscular |
Inheritance | autosomal recessive with age-dependent incomplete penetrance; a risk factor associated with DM is detected. |
Age of onset | ab 8 years |
Causality | High-risk factor |
Gene | SOD1 |
Mutation | G-A |
Literature | OMIA:000263-9615 |
Juvenile laryngeal paralysis & polyneuropathy (JLPP)
Test specifications
Symptom complex | neurological |
Inheritance | autosomal recessive |
Age of onset | 3 months |
Causality | causally |
Gene | RAB3GAP1 |
Mutation | DEL |
Literature | OMIA:001970-9615 |