CHOVNÁ FENA, výška 52 cm, hlava typická, špičatější čenich, výraznější nadočnicové oblouky, ucho nížeji nasazené, větší, korektně nesené, oko mandlové, správně uloženo, obě oči hnědé, chrup nadpočetný, zdvojená P1 vpravo nahoře, skus těsný nůžkový, krk dle standardu, hrudník hluboký, prostorný, hřbet rovný, silný, záď lehce spáditá, břicho dle standardu, postoj hrudních končetin lehce sbíhavý, volné lokty, končetina silná, úhlení předních končetin korektní, postoj pánevních končetin korektní, hlezna krátká, kolmá, rovnoběžná, úhlení zadních končetin korektní, ocas dlouhý, nekupírovaný, zálomek v poslední 1/3, srst střední textury a délky, barva dle standardu, rozlité pálení na hlavě a na stehnech, pigmentace odpovídá barvě srsti, víčka, pysky i nosní houba plně pigmentované, pohybová mechanika měkká, volná, plynulá, vyvážená, vzadu užší, pohlavní výraz vyjádřen správně, kondice výstavní, celkový vzhled vyvážený, střední velikosti a kostry, správného rámce, povaha vyrovnaná, živá, pozorná. Slabá reakce na střelbu.

Povahový test: 10 – 10 – 16 – 5 – 10 – 14 – 10 – 10 – 9 = 94 bodů/A.

(19.6.2016 Pňov, rozh. Alexandra Grygarová)

16.9.2017 Coursing - MR ČR, Ptýrov - nechrti - 1.místo AUO - Mistr ČR (7 závodníků) - 353 b.
11.9.2016 Coursing - Klubový závod, Ptýrov - sk. I - 1. místo (4 závodníci) - 345 b. - Nejlepší fena
21.8.2016 Coursing - Mistrovství Čech, Ješín - australský ovčák - 2. místo (4 závodníci) - 352 b.

18.9.2016 Genoscoper Laboratories
DNA Hyperuricosuria, (HUU) - clear
DNA Neuronal Ceroid Lipofuscinosis 8, (NCL8) - clear
DNA Craniomandibular Osteopathy, (CMO) - clear
DNA Color Locus E - Extensions - E/E
DNA Color Locus B - Brown - B/bs || bs/bd
DNA Color Locus K - Dominant Black - ky/ky
DNA Color Locus A - Agouti - at/at
DNA Color Locus S - Piebald or extreme white spotting - S/S
DNA Color Locus H - Harlequin - h/h
DNA Furnishings / Improper Coat in Portuguese Water Dogs (marker test) - GG/CC
DNA Tiny size, insulin-like growth factor 1 receptor (IGF1R) gene variant - G/G
DNA Ear erectness (pricked ears versus floppy ears), variant chr10:11072007 - T/T
DNA Bobtail - C/C
DNA Snout/skull length (shortened head versus elongated head), bone morphogenetic protein 3 (BMP3) gene variant - C/C
DNA Color Locus C - Albinism (caL-allele) - C/C
DNA Body mass, insulin-like growth factor 1 (IGF1) gene variant - G/G
DNA Coat length, FGF5 gene variant - T/T
DNA Curly coat - C/C
DNA Color Pattern (RALY gene): Saddle Tan - dup/dup
DNA Bleeding disorder due to P2RY12 defect - clear
DNA Canine Cyclic Neutropenia, Cyclic Hematopoiesis, Gray Collie Syndrome, (CN) - clear
DNA Canine Leukocyte Adhesion Deficiency (CLAD), type III - clear
DNA Canine Scott Syndrome, (CSS) - clear
DNA Factor IX Deficiency or Hemophilia B (4 mutations) - clear
DNA Factor VII Deficiency - clear
DNA Factor VIII Deficiency or Hemophilia A (3 mutations) - clear
DNA Factor XI Deficiency - clear
DNA Glanzmann Thrombasthenia Type I, (GT); mutation originally found in Pyrenean Mountain Dog - clear
DNA Hereditary Elliptocytosis - clear
DNA Hereditary Phosphofructokinase (PFK) Deficiency - clear
DNA Macrothrombocytopenia; disease-linked variant originally found in Norfolk and Cairn Terrier - clear
DNA May-Hegglin Anomaly (MHA) - clear
DNA Prekallikrein Deficiency - clear
DNA Pyruvate Kinase Deficiency (4 mutations) - clear
DNA Thrombopathia (3 mutations) - clear
DNA Trapped Neutrophil Syndrome, (TNS) - clear
DNA Von Willebrand's Disease (vWD) Type I - clear
DNA Von Willebrand's Disease (vWD) Type II - clear
DNA Von Willebrand's Disease (vWD) Type III (3 mutations) - clear
DNA Canine Multifocal Retinopathy 2, (CMR2); mutation originally found in Coton de Tulear - clear
DNA Canine Multifocal Retinopathy 3, (CMR3); mutation originally found in Lapponian Herder - clear
DNA Cone Degeneration, (CD) or Achromatopsia (2 mutations) - clear
DNA Cone-Rod Dystrophy 1, (crd1); mutation originally found in American Staffordshire Terrier - clear
DNA Cone-Rod Dystrophy 2, (crd2); mutation originally found in Pit Bull Terrier - clear
DNA Cone-Rod Dystrophy, (cord1-PRA / crd4) Autosomal Recessive - clear
DNA Cone-Rod Dystrophy, Standard Wirehaired Dachshund, (crd SWD) - clear
DNA Congenital Stationary Night Blindness (CSNB) - clear
DNA Dominant Progressive Retinal Atrophy, (DPRA) - clear
DNA Early Retinal Degeneration, (erd); mutation originally found in Norwegian Elkhound - clear
DNA Generalized Progressive Retinal Atrophy - clear
DNA Golden Retriever Progressive Retinal Atrophy 1, (GR_PRA 1) - clear
DNA Primary Lens Luxation, (PLL) - clear
DNA Primary Open Angle Glaucoma, (POAG); mutation originally found in Beagle - clear
DNA Primary Open Angle Glaucoma, (POAG); mutation originally found inNorwegian Elkhound - clear
DNA Progressive Retinal Atrophy Type III, (PRA type III); mutation originally found in Tibetan Spaniel and Tibetan Terrier - clear
DNA Progressive Retinal Atrophy, (CNGA1-PRA); mutation originally found in Shetland Sheepdog - clear
DNA Progressive Retinal Atrophy, (PAP1_PRA); mutation originally found in Papillon and Phalene - clear
DNA Progressive Retinal Atrophy, (PRA); mutation originally found in Basenji - clear
DNA Rod-Cone Dysplasia 1, (rcd1) and Rod-Cone Dysplasia 1a, (rdc1a) (2 mutations) - clear
DNA Rod-Cone Dysplasia 3, (rcd3) - clear
DNA X-Linked Progressive Retinal Atrophy 1, (XLPRA1) - clear
DNA X-Linked Progressive Retinal Atrophy 2, (XLPRA2) - clear
DNA Long QT Syndrome - clear
DNA Congenital Hypothyroidism; mutation originally found in Toy Fox- and Rat Terrier - clear
DNA Autosomal Recessive Severe Combined Immunodeficiency, (ARSCID) - clear
DNA Complement 3 (C3) Deficiency - clear
DNA Myeloperoxidase Deficiency - clear
DNA Severe Combined Immunodeficiency in Frisian Water Dogs, (SCID) - clear
DNA X-linked Severe Combined Immunodeficiency (XSCID) (2 mutations) - clear
DNA Cystinuria Type I-A; mutation originally found in Newfoundland Dog - clear
DNA Cystinuria Type II-A and Cystinuria Type II-B (2 mutations) - clear
DNA Fanconi Syndrome - clear
DNA Polycystic Kidney Disease in Bull Terriers, (BTPKD) - clear
DNA Primary Hyperoxaluria, (PH); mutation originally found in Coton de Tulear - clear
DNA Protein Losing Nephropathy, (PLN); NPHS1 gene variant - clear
DNA Renal Cystadenocarcinoma and Nodular Dermatofibrosis, (RCND) - clear
DNA X-Linked Hereditary Nephropathy, (XLHN) (2 mutations) - clear
DNA Glycogen Storage Disease Type II or Pompe's Disease, (GSD II) - clear
DNA Glycogen Storage Disease Type IIIa, (GSD IIIa) - clear
DNA Glycogen Storage Disease Type Ia, (GSD Ia) - clear
DNA Hypocatalasia or Acatalasemia - clear
DNA Intestinal Cobalamin Malabsorption or Imerslund-Gräsbeck Syndrome, (IGS) (2 mutations) - clear
DNA Mucopolysaccharidosis Type IIIA, (MPS IIIA) (2 mutations) - clear
DNA Mucopolysaccharidosis Type VII, (MPS VII) (2 mutations) - clear
DNA Pyruvate Dehydrogenase Phosphatase 1 (PDP1) Deficiency - clear
DNA Cavalier King Charles Spaniel Muscular Dystrophy, (CKCS-MD) - clear
DNA Centronuclear Myopathy, (CNM) (2 mutations) - clear
DNA Duchenne or Dystrophin Muscular Dystrophy, (DMD); mutation originally found in Golden Retriever - clear
DNA Duchenne or Dystrophin Muscular Dystrophy, (DMD); mutation originally found in Norfolk Terrier - clear
DNA Muscular Dystrophy (MDL), Ullrich-type; mutation originally found in Landseer - clear
DNA Muscular Hypertrophy (Double Muscling) - clear
DNA Myotonia Congenita (2 mutations) - clear
DNA X-Linked Myotubular Myopathy (2 mutations) - clear
DNA Alaskan Husky Encephalopathy, (AHE) - clear
DNA Bandera's Neonatal Ataxia, (BNAt) - clear
DNA Benign Familial Juvenile Epilepsy or Remitting Focal Epilepsy - clear
DNA Cerebral Dysfunction; mutation originally found in Friesian Stabyhoun - clear
DNA Dandy-Walker-Like Malformation (DWLM); mutation originally found in Eurasier - clear
DNA Early-Onset Progressive Polyneuropathy (2 mutations) - clear
DNA Fetal Onset Neuroaxonal Dystrophy, (FNAD) - clear
DNA Hereditary Ataxia or Cerebellar Ataxia; mutation originally found in Old English Sheepdog and Gordon Setter - clear
DNA Hyperekplexia or Startle Disease - clear
DNA Hypomyelination; mutation originally found in Weimaraner - clear
DNA L-2-Hydroxyglutaric aciduria, (L2HGA); mutation originally found in Staffordshire Bull Terrier - clear
DNA Lagotto Storage Disease, (LSD) - clear
DNA Neonatal Cerebellar Cortical Degeneration or Cerebellar Abiotrophy,(NCCD) - clear
DNA Neonatal Encephalopathy with Seizures, (NEWS) - clear
DNA Neuroaxonal Dystrophy (NAD); mutation originally found in Spanish Water Dog - clear
DNA Neuronal Ceroid Lipofuscinosis 1, (NCL1); mutation originally found inDachshund - clear
DNA Neuronal Ceroid Lipofuscinosis 10, (NCL10); mutation originally found in American Bulldog - clear
DNA Neuronal Ceroid Lipofuscinosis 12, (NCL12) - clear
DNA Neuronal Ceroid Lipofuscinosis 4A, (NCL4); mutation originally found in American Staffordshire Terrier - clear
DNA Neuronal Ceroid Lipofuscinosis 5, (NCL5); mutation originally found in Border Collie - clear
DNA Neuronal Ceroid Lipofuscinosis 8, (NCL8); mutation originally found in English Setter - clear
DNA Neuronal Ceroid Lipofuscinosis, (NCL7); mutation originally found in Chinese Crested Dog and Chihuahua - clear
DNA Progressive Early-Onset Cerebellar Ataxia; mutation originally found in Finnish Hound - clear
DNA Spinal Dysraphism - clear
DNA Spinocerebellar Ataxia with Myokymia and/or Seizures (SCA) - clear
DNA Spinocerebellar Ataxia/ Late-Onset Ataxia (SCA, LOA) - clear
DNA X-Linked Tremors; mutation originally found in English Springer Spaniel - clear
DNA Congenital Myasthenic Syndrome, (CMS); mutation originally found in Jack Russell Terrier - clear
DNA Congenital Myasthenic Syndrome (CMS); mutation originally found in Labrador Retriever - clear
DNA Congenital Myasthenic Syndrome, (CMS); mutation originally found in Old Danish Pointing Dog - clear
DNA GM1 Gangliosidosis (3 mutations) - clear
DNA GM2 Gangliosidosis or Sandhoff Disease (2 mutations) - clear
DNA Globoid Cell Leukodystrophy or Krabbe's Disease, (GLD) (2 mutations) - clear
DNA Chondrodysplasia; mutation originally found in Norwegian Elkhound and Karelian Bear Dog - clear
DNA Cleft Palate; Cleft Lip and Palate with Syndactyly; DLX6 gene mutation originally found in Nova Scotia Duck Tolling Retriever - clear
DNA Cleft Palate; Cleft Lip and Palate with Syndactyly; ADAMTS20 gene mutation originally found in Nova Scotia Duck Tolling Retriever - clear
DNA Hereditary Vitamin D-Resistant Rickets, (HVDRR) - clear
DNA Oculoskeletal Dysplasia 2 or Dwarfism-Retinal Dysplasia 2, (OSD2) - clear
DNA Osteochondrodysplasia; mutation originally found in Miniature Poodle - clear
DNA Osteogenesis Imperfecta, (OI); mutation originally found in Beagle - clear
DNA Osteogenesis Imperfecta, (OI); mutation originally found in Dachshund - clear
DNA Skeletal Dysplasia 2, (SD2) - clear
DNA Spondylocostal Dysostosis - clear
DNA Van den Ende-Gupta Syndrome, (VDEGS) - clear
DNA Dystrophic Epidermolysis Bullosa (2 mutations) - clear
DNA Epidermolytic Hyperkeratosis - clear
DNA Focal Non-Epidermolytic Palmoplantar Keratoderma (FNEPPK/DH) - clear
DNA Hereditary Footpad Hyperkeratosis, (HFH) - clear
DNA Golden Retriever Ichthyosis - clear
DNA Ichthyosis; mutation originally found in Great Dane - clear
DNA Lamellar Ichthyosis, (LI) - clear
DNA Ligneous Membranitis - clear
DNA Musladin-Lueke syndrome, (MLS) - clear
DNA X-Linked Ectodermal Dysplasia, (XHED) - clear
DNA Malignant Hyperthermia (MH) - clear
DNA Amelogenesis Imperfecta, (AI) - clear
DNA Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis, (CKCSID) - clear
DNA Dental Hypomineralization; mutation originally found in Border Collie - clear
DNA Narcolepsy (3 mutations) - clear
DNA Persistent Müllerian Duct Syndrome, (PMDS); mutation originally found in Miniature Schnauzer - clear
DNA Primary Ciliary Dyskinesia, (PCD) – clear