HOPSCOTCH Mera (Mera)
- Colour: BLACK
- Coat: FLEECE
- Size / Height to Withers (Weight): MEDIUM / (14kg)
- DNA Profile: ORIVET 20203948
- GENETIC TRAITS: Associated with Phenotype
- A LOCUS (Fawn/Sable, Tri/Tan): a[y]/a[t]
- BLACK AND TAN/SADDLE COAT COLOUR: CARRIER - ONE COPY
- K LOCUS (Dominant Black): K/k[y] or k[br]
- BROWN (345DELPRO) DELETION: B/b[d]
- BROWN (GLNT331STOP) STOP CONDON: B/B[s]
- BROWN (SER41CYS) INSERTION CONDON: B/b[c]
- D (Dilute) LOCUS: D/D
- E LOCUS (Cream / Red / Yellow): E/e
- I Locus Colour Intensity: I/I
- PIED: S/S
- EM (MC1R) LOCUS - MELANISTIC MASK: E[m]/E[n]
- CURLY COAT (R151W): ONE COPY
- IMPROPER COAT (RSPO2) - FURNISHINGS: NEGATIVE
- COAT COMPOSITION (Double/Single): UDC/UDC - NO COPY OF THE DOUBLE COAT
- LONG HAIR GENE (Canine C95F): POSITIVE
- HEREDITARY DISEASE DNA TEST RESULTS: Orivet GENO 5.0 - Clear of All Screenable Genetic Diseases 21 BREED SPECIFIC RESULTS LISTED BELOW
- Canine Hyperuricosuria (SLC2A9): CLEAR BY PARENTAGE
- Centronuclear Myopathy (Labrador Retriever Type) (HACD1): CLEAR BY PARENTAGE
- Congenital Myasthenic Syndrome (Labrador Retriever Type) (COLQ): CLEAR BY PARENTAGE
- Cystinuria Labrador Retriever Type - CYN (SLC3A1): CLEAR BY PARENTAGE
- Degenerative Myelopathy - DM (SOD1): CLEAR BY PARENTAGE
- Elliptocytosis B-spectrin (Labrador Retriever/Poodle Type) (SPTB): CLEAR BY PARENTAGE
- Exercise Induced Collapse (Retriever Type) (EIC): CLEAR BY PARENTAGE
- Gangliosidosis GM2 (Poodle Type) (HEXB): CLEAR BY PARENTAGE
- Hereditary Nasal Parakeratosis/Dry Nose (Labrador Retriever Type) (SUV39H2): CLEAR BY PARENTAGE
- Hyperuricosuria: CLEAR BY PARENTAGE
- Macular Corneal Dystrophy (Labrador Type) (LOC4): CLEAR BY PARENTAGE
- Malignant Hyperthermia (RYR1): CLEAR BY PARENTAGE
- Mucopolysaccharidosis VI (Poodle Type): CLEAR BY PARENTAGE
- Myotubular Myopathy X-linked (MTM1): CLEAR BY PARENTAGE
- Myotubular Myopathy X-Linked (Labrador Retriever Type) (MTM1): CLEAR BY PARENTAGE
- Narcolepsy (Labrador) (HCRTR2): CLEAR BY PARENTAGE
- Neonatal Encephalopathy (Poodle Type) (ATF2): CLEAR BY PARENTAGE
- Progressive Rod Cone Degeneration - PRA (PRCD): CLEAR BY PARENTAGE
- Pyruvate Kinase Deficiency (Labrador Type) (PKLR): CLEAR BY PARENTAGE
- Skeletal Dysplasia 2 (Mild Disproportionate Dwarfism) (COL11A2): CLEAR BY PARENTAGE
- von Willebrand's Disease Type I - VWDI (VWF): CLEAR BY PARENTAGE
