MHOC (MALADIE HÉRÉDITAIRE OCULAIRE CANINE) : INDEMNE

• Aurelie Sauvage
• 17 Tue Jun

MERLE : m/[Mc(223 )]/M (266)

ested dog is a mosaic for tested 5/LV gene and carries an additional M* allele in some cells; the phenotypic impact and inheritance of the additional allele cannot be predicted as cell distribution throughout the body may be variable.

• EVG
• 19 Thu Jun

PRA-PRCD (Atrophie Progressive de la Rétine) : +/-

19 Jun 25

PRA-PRCD (ATROPHIE PROGRESSIVE DE LA RÉTINE) : +/+

• EVG
• 19 Thu Jun

AOC (ANOMALIE DE L’OEIL DU COLLEY) : +/+

• EVG
• 19 Thu Jun

DM (MYÉLOPATHIE DÉGÉNÉRATIVE) : +/+

• EVG
• 19 Thu Jun

MDR1 (Sensibilité Médicamenteuse) : +/+

• EVG
• 19 Thu Jun

NATURAL BOBTAIL : N/N

• EVG
• 19 Thu Jun

HUU (HYPERURICOSURIA) : +/+

The test examines presence or absence of SLC2A9 gene mutation ( c. 616G> T) described as the cause of hyperuricosuria (HU) in many dog breeds. The disease is characterized by an excessive excretion of uric acid into urine, leading to formation of uric acid stones. Hyperuricosuria is inherited as an autosomal recessive trait.

• EVG
• 19 Thu Jun

NCL-6 (NEURONAL CEROID LIPOFUSCINOSIS 6) : +/+

The test examines presence or absence of CLN6 gene mutation (c.829T>C) described as the cause of neuronal ceroid lipofuscinosis (NCL6) in Australian Shepherd. The disease is characterized by neurodegeneration, which causes psychological abnormalities and ataxia. Neuronal ceroid lipofuscinosis is inherited as an autosomal recessive trait.

• EVG
• 19 Thu Jun

CMRl (CANINE MULTIFOCAL RETINOPATHY1YPE 1) : +/+

The test examines presence or absence of BESTl gene mutation (c.73C>T) described as the cause for canine multifocal retinopathy (CMRl) in several dog breeds. Causative mutation in BESTl gene generates a premature stop codon, which results in non-functional protein responsible for proper formation of pigment epithelium in retina. CMRl is inherited as an autosomal recessive trait.

• EVG
• 19 Thu Jun