RALLEE Certified Canine Genetic Testing Panel 3
$1,549.00
For symptoms involving: Blood, Cancer, Endocrine System, Gastrointestinal Tract, Heart, Immune System, Kidneys, Liver, Metabolism, Respiratory Tract
RALLEE® Certified Canine Genetic Testing Panel 3
RALLEE® Certified Canine Genetic Testing Panel 3 includes genetic testing for diseases with symptoms involving blood, cancer, endocrine system, gastrointestinal tract, heart, immune system, kidneys, liver, metabolism, and respiratory system that may be difficult to accurately diagnose clinically due to rarity or broad symptoms that are common to multiple diseases. Understanding the specific genetic cause for your dog’s symptoms allows your veterinarian to identify the best treatment possible, potentially including enrollment in experimental therapies.
Number of Alleles Tested: 135 | |
Condition |
Gene(s) |
Acute Respiratory Distress Syndrome | ANLN |
Bernard-Soulier Syndrome Type C | GP9 |
C3 Deficiency | C3 |
Cardiomyopathy | YARS2 |
Ciliary Dyskinesia 1, 2 | CCDC39, NME5 |
Colorectal Hamartomatous Polyposis and Ganglioneuromatosis | PTEN |
Congenital Dyshormonogenic Hypothyroidism | SLC5A5 |
Copper Toxicosis | COMMD1 |
Cushing’s Syndrome 1-6 | GNAS |
Cyclic Neutropenia | AP3B1 |
Cystinuria Type IA | SLC3A1 |
Cystinuria Type IIA 1, 2 | SLC3A1 |
Cystinuria Type IIB | SLC7A9 |
Demyelinating Peripheral Neuropathy | SBF2 |
Diffuse Cystic Renal Dysplasia and Hepatic Fibrosis | INPP5E |
Dilated Cardiomyopathy | PLN |
Elliptocytosis | SPTB |
Exercise Induced Metabolic Myopathy | ACADVL |
Factor VII Deficiency | F7 |
Factor XI Deficiency | F11 |
Fanconi Syndrome | FAN1 |
Fatal Neonatal Interstitial Lung Disease | LAMP3 |
Gallbladder Mucoceles | ABCB4 |
Gastrointestinal Stromal Tumors 1-6 | KIT |
Glycogen Storage Disease Ia | G6PC |
Glycogen Storage Disease IIIa | AGL |
Glycogen Storage Disease VII 1, 2 | PFKM |
Hemophilia A 1-5 | F8 |
Hemophilia B 1-7 | F9 |
Hepatic Copper Toxicosis | ATP7B |
Hereditary Nephritis | COL4A5 |
Hereditary Methemoglobinemia 1, 2 | CYB5R3 |
Hereditary Nephropathy 1-3 | COL4A4, COL4A5 |
Hypocatalasia | CAT |
Hypothyroidism 1-4 | TPO |
Inflammatory Pulmonary Disease | AKNA |
Intestinal Cobalamin Malabsorption | AMN |
Invasive Transitional Cell Carcinoma | BRAF |
Laryngeal Paralysis Risk Factor | RAPGEF6 |
Lethal Acrodermatitis | MKLN1 |
Leukocyte Adhesion Deficiency | FERMT3 |
Leukocyte Adhesion Deficiency Type I | ITGB2 |
Ligneous Membranitis | PLG |
Lundehund Syndrome | LEPREL1 |
Malignant Hyperthermia | RYR1 |
May-Hegglin Anomaly | MYH9 |
Mucopolysaccharidosis Type I | IDUA |
Mucopolysaccharidosis Type VI 1, 2 | ARSB |
Myeloperoxidase Deficiency | MPO |
Myotubular Myopathy 1, 2 | MTM1 |
Obesity and Food Motivation | POMC |
Oculocutaneous Albinism Type IV 1-3 | SLC45A2 |
Pancreatitis Variant 1-3 | SPINK1 |
Periodic Fever Syndrome 1,2 | HAS2, MTBP |
Pituitary Dwarfism | LHX3 |
Polycystic Kidney Disease | PKD1 |
Pompe Disease | GAA |
Postoperative Hemorrhage | P2RY12 |
Prekallikrein Deficiency | KLKB1 |
Primary Hyperoxaluria | AGXT |
Primary Polycythemia 1 | JAK2 |
Protection Against Liver Copper Accumulation | ATP7A |
Pyruvate Dehydrogenase Deficiency | PDP1 |
Pyruvate Kinase Deficiency of Erythrocyte 1-6 | PKLR |
Renal Cystadenocarcinoma | FLCN |
Scott Syndrome | ANO6 |
Selective Cobalamin Malabsorption 1-3 | CUBN |
Severe Combined Immunodeficiency Disease 1,2 | PRKDC, RAG1 |
Squamous Cell Carcinoma | KITLG |
Thrombasthenia 1-3 | ITGA2B |
Thrombocytopenia 1, 2 | TUBB1 |
Thrombopathia 1-3 | RASGRP1 |
Trapped Neutrophil Syndrome | VPS13B |
Upper Airway Syndrome | ADAMTS3 |
Urolithiasis | SLC2A9 |
Vitamin D Deficiency Rickets Type II | VDR |
Von Willebrand Disease Type I | VWF |
Von Willebrand Disease Type II 1, 2 | VWF |
Von Willebrand Disease Type III 1-3 | VWF |
X-linked Severe Combined Immunodeficiency 1, 2 | IL2RG |