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Combination Lagotto Romagnolo

General description

includes: Hyperurikosuria (HUU/SLC), Juvenile epilepsy (JE), Lagotto storage disease (LSD), Neuroaxonal dystrophy (NAD), Progressive retinal atrophy (prcd-PRA)*** and Furnishing (wire hair)

Breeds

Lagotto Romagnolo

Order details
Test number8499
Sample material0.5 ml EDTA blood, 2x cheek swab, 1x special swab (eNAT)
Test duration7-14 working days

Hyperuricosuria (HUU/SLC)

Test specifications
Symptom complexurological
Inheritanceautosomal recessive
Causalitycausally
GeneSLC2A9
MutationG-T
LiteratureOMIA:001033-9615

Furnishing (wire hair)

Test specifications
Inheritanceautosomal dominant
GeneRSPO2
MutationCOMPLEX
LiteratureOMIA:001531-9615

Lagotto storage disease (LSD)

Test specifications
Symptom complexneurological
Inheritanceautosomal recessive with incomplete penetrance
Age of onset4 months - 4 years
Causalitycausally
GeneATG4D
MutationC-T
LiteratureOMIA:001954-9615

Juvenile epilepsy (JE)

Test specifications
Symptom complexneurological
Inheritanceautosomal recessive
Age of onset5-12 weeks
Causalitycausally
GeneLGI2
MutationA-T
LiteratureOMIA:001596-9615

Progressive retinal atrophy (prcd-PRA)

Test specifications
Symptom complexophthalmic
Inheritanceautosomal recessive
Causalitycausally
GenePRCD
MutationC-T
LiteratureOMIA:001298-9615