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):KB/k[y] or k[br]
- BROWN (345DELPRO) DELETION:B[d]/b[d]
- BROWN (GLNT331STOP) STOP CONDON:B[s]/B[s]
- BROWN (SER41CYS) INSERTION CONDON:B[c]/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
