When your veterinarian suspects a genetic cause for your cat’s otherwise unexplainable symptoms, MoxxiTech is here to help.
RALLEE® Certified Feline Diagnostic Panel 2 includes genetic testing for diseases with symptoms involving development, musculoskeletal system, skin and hair that may be difficult to accurately diagnose clinically due to rarity or due to broad symptoms that are common to multiple diseases. Understanding the specific genetic cause for your cat’s symptoms allows your veterinarian to identify the best treatment possible, potentially including enrollment in experimental therapies.
Learn more about genetic testing Order a Sample Collection Kit Veterinarians: Order Now
Click Here to View the Genes and Conditions included in Feline Diagnostic Panel 2
For symptoms involving: Development, Musculoskeletal System, Skin and Hair
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Number of Alleles Tested: 45 |
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Condition |
Gene(s) |
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Acute Intermittent Porphyria (AIP) 1-6 |
HMBS |
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Alpha Mannosidosis |
MAN2B1 |
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Brachycephaly and Craniofacial Defects |
ALX1 |
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Chediak-Higashi Syndrome |
LYST |
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Congenital Hypothyroidism |
TPO |
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Dihydropyrimidinase (DHP) |
CPYS |
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Ehlers-Danlos Syndrome, Classic Type I (EDS) |
COL5A1 |
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Erythrocyte Pyruvate Kinase Deficiency (PK Deficiency) |
PKLR |
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Erythropoietic Porphyria |
UROS |
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Fibrodysplasia Ossificans |
ACVR1 |
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Glycogen Storage Disease Type IV (GSD IV) |
GBE |
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GM1 Gangliosidosis 1-5 |
GLB1, GM2A, HEXB |
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Hairless with shortened lifespan |
FOXN1 |
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Hemophilia B 1, 2 |
F9 |
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Hyperlipoproteinaemia |
LPL |
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Hypokalemic Periodic Paralysis |
WNK4 |
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Inflammatory Linear Verrucous Epidermal Nevus (ILVEN) |
NSDHL |
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Mucolipidosis Type II |
GNPTAB |
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Mucopolysaccharidosis Type I |
IDUA |
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Mucopolysaccharidosis Type VI |
ARSB |
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Mucopolysaccharidosis VII 1, 2 |
GUSB |
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Myotonia Congenita |
CLCN1 |
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Neuronal Ceroid Lipofuscinosis Type 7 (CLN7) |
MFSD8 |
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Niemann-Pick Disease Type C1 (NPC1) 1, 2 |
NPC1 |
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Niemann-Pick Disease Type C2 (NPC2) |
NPC2 |
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Osteochondrodysplasia |
TRPV4 |
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Rickets Type I 1, 2 |
CYP27B1, CYP27B2 |
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Rickets Type IB |
CYP2R1 |
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Spasticity (Congenital Myasthenic Syndrome, CMS) |
COLQ |
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Spinal Muscular Atrophy |
LIX1 |
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Testicular Hypoplasia and Persistent Primary Dentition |
TAC3 |