SALUKI DNA test Results sent direct to KC Owner submission to KC Not recorded by the Kennel Club AB required AB rec'd Patent SAMOYED

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Transcription:

SALUKI Progressive Retinal Atrophy (PRA) Degenerative Myleopathy Coat length/texture SAMOYED Degenerative Myleopathy Hereditary Nephritis (HN) Progressive Retinal Atrophy, X-Linked (PRA-XL) Retinal Dysplasia / Ocularskeletal Dysplasia

(OSD) Coat Length / Texture Coat Colour Gene Variations SCHIPPERKE Mucopolysaccharidosis (MPS) IIIB PennGen YES von Willebrnd's disease type 1 (vwd1) Progressive Retinal Atrophy, prcd (prcd-pra)* YES Bobtail Gene Coat Colour Gene Variations Coat Length (long hair gene)

SCHNAUZER Dilated Cariomyopathy OFA (DCM) University of Missouri SCOTTISH TERRIER Primary Lens Luxation (PLL) Craniomandibular Osteopathy (CMO) von Willebrand's disease (vwd) type 3 Coat Colour Gene Variations SEALYHAM TERRIER Primary Lens Luxation (PLL) YES

Degenerative Myleopathy Coat Colour Gene Variations SEGUGIO ITALIANO Myeloperoxidase Deficiency SHAR PEI POAG/PLL YES Shar Pei auto-inflammatory disease (SPAID) Coat Colour Gene Variations SHETLAND SHEEPDOG * Collie Eye Anomaly/Choroidal * * YES YES Hypoplasia (CEA/CH)* * * van Haeringen *

Multi Drug Resistance (MDR1) von Willebrand's disease (vwd) Type 3 Progressive Retinal Atrophy (CNGA1-PRA) Dermatomyositis (DMS) Degenerative Myelopathy Leukoencephalomyelopathy SHIH TZU Thrombocytopaenia Degenerative Myelopathy Prekallikrein Deficiency

Coat Colour Gene Variations SIBERIAN HUSKY Degenerative Myleopathy Progressive Retinal Atrophy, prcd (prcd-pra)* YES Cone Degeneration Progressive Retinal Atrophy, X-Linked (PRA-XL) Gangliosidosis (GM1) Warbung Micro Syndrome 1 Coat Length / Texture Coat Colour Gene Variations

SKYE TERRIER Coat Colour Gene Variations SLOUGHI Progressive Retinal Atrophy rcd1a (PRA-rcd1a) Coat Colour Gene Variations van Haeringen SMALL MUNSTERLANDER Progressive Retinal Atrophy, rcd4 (PRA-rcd4) Coat Colour Gene Variations SOFT-COATED WHEATEN TERRIER Protein Losing Nephropathy (PLN) PennVet Degenerative Myelopathy Paroxysmal Dyskinesia OFFA

(PxD) Curly coat test Coat Colour Gene Variations SPANIEL (AMERICAN COCKER) Progressive Retinal Atrophy, YES YES prcd (prcd-pra) * Exercise Induced Collapse (EIC) Pinmoore Animal Laboratory Services Phosphofructokinase Deficiency (PFK) DDC PennGen

Familial Nephropathy (FN) Iron Refractory Iron Deficiency Anaemia (IRIDA) PennGen SPANIEL (CLUMBER) Pyruvate Dehydrogenase Phosphatase Deficiency (PDP1) OFFA YES Exercise Induced Collapse (EIC) YES Degenerative Myelopathy Phosphofructokinase Deficiency (PFK) SPANIEL (COCKER) Familial Nephropathy (FN) YES

Progressive Retinal Atrophy, * * prcd (prcd-pra)* * YES YES Acral Mutilation * * van Haeringen * Syndrome (AMS) Adult Onset Neuropathy (AON) OFFA Degenerative Myelopathy Phosphofructokinase Deficiency (PFK) Exercise Induced Collapse (EIC) PennGen Iron Refractory Iron Deficiency Anaemia (IRIDA) PennGen Genoscoper (MyDgDNA)

SPANIEL (ENGLISH SPRINGER) Fucosidosis PennGen YES Progressive Retinal Atrophy, cord1 (PRA-cord1) YES OFFA Phosphofructokinase Deficiency (PFK) PennGen YES Acral Mutilation OFFA Syndrome (AMS) Familial Nephropathy (FN) Degenerative Myelopathy X-linked Tremor Genocscoper (MyDogDNA)

Malignant Hyperthermia (MH) SPANIEL (FIELD) Phosphofructokinase Deficiency (PFK) Progressive Retinal Atrophy, cord1 (PRA-cord1) SPANIEL (IRISH WATER) Phosphofructokinase Deficiency (PFK) Coagulation Factor V11 Deficiency SPANIEL (SUSSEX)

Phosphofructokinase Deficiency (PFK) Pyruvate Dehydrogenase Phosphatase Deficiency (PDP1) OFFA SPANIEL (WELSH SPRINGER) Familial Nephropathy (FN) Factor VII Deficiency Genoscoper SPANISH WATER DOG Progressive Retinal Atrophy, * * prcd (prcd-pra) * * YES YES Neuroaxonal Dystrophy * * (NAD) Congential Hypothyroidism with goiter (CHG)

Hyperuricosuria (HUU) Bobtail gene STAFFORDSHIRE BULL TERRIER Hereditary Cataract (HC-HSF4) YES OFFA L-2 Hydroxyglutaric Aciduria (L2-HGA) YES Degenerative Myelopathy

ST BERNARD Degenerative Myleopathy Juvenile-onset Inherited Polyneuropathy Coat Colour Gene Variations Coat length / texture SWEDISH LAPPHUND Progressive Retinal Atrophy, prcd (prcd-pra)* YES Pompe's disease (GSD II) Bobtail gene Coat Colour Gene Variations

SWEDISH VALLHUND Retinopathy Hyperuricosuria (HUU) Bobtail gene Coat Length / texture Genoscoper (MyDpgDNA)