When your veterinarian suspects a genetic cause for your dog’s otherwise unexplainable symptoms, MoxxiTech is here to help.
RALLEE® Certified Canine Diagnostic Panel 2 includes genetic testing for diseases with symptoms involving development, musculoskeletal system, reproduction, skin and hair, and teeth and oral cavity 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 dog’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 Canine Diagnostic Panel 2
Canine Diagnostic Panel 2 Genes and Conditions
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Number of Alleles Tested: 160 |
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Condition |
Gene(s) |
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Abortion |
BTBD17 |
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Alexander Disease |
GFAP |
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Amelogenesis Imperfecta 1-3 |
ACP4, ENAM |
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Bernard-Soulier Syndrome Type C |
GP9 |
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Beta Mannosidosis 1, 2 |
MANBA |
|
Centronuclear Myopathy 1, 2 |
BIN1, HACD1 |
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CHILD-like Syndrome |
NSDHL |
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Chondrodysplasia |
ITGA10 |
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Chondrodystrophy (HT1) |
CFA 12 |
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Ciliary Dyskinesia 1, 2 |
CCDC39, NME5 |
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Cleft Lip and Palate |
ADAMTS20 |
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Cleft Palate |
DLX6 |
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Coat Color Dilution (d^1, d^2) |
MLPH |
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Congenital Ichthyosis |
NIPAL4 |
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Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis |
FAM83H |
|
Congenital Myasthenic Syndrome 1-4 |
CHAT, CHRNE, COLQ |
|
Craniomandibular Osteopathy 1-4 |
SLC37A2, COL1A1, SLC35D1 |
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Cushing’s Syndrome 1-6 |
GNAS |
|
Cyclic Neutropenia |
AP3B1 |
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Decreased Fecundity |
GDF9 |
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Dental Hypomineralization |
FAM20C |
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Dermatosparaxis |
ADAMTS2 |
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Dermoid Sinus |
FGF3 |
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Disorder of Sexual Development |
HSD17B3 |
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Disproportionate Dwarfism |
COL11A2 |
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Dystrophic Epidermolysis Bullosa 1, 2 |
COL7A1 |
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Ectodermal Dysplasia, 1-2 |
FOXI3, PKP1 |
|
Ehlers-Danlos Syndrome 1-4 |
COL5A1, TNXB |
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Epidermolysis Bullosa |
PLEC |
|
Epidermolytic Hyperkeratosis |
KRT10 |
|
Episodic Falling Syndrome |
BCAN |
|
Exercise Induced Collapse |
DNM1 |
|
Exercise Induced Metabolic Myopathy |
ACADVL |
|
Exfoliative Cutaneous Lupus Erythematosus (ECLE) |
UNC93B1 |
|
Fanconi Syndrome |
FAN1 |
|
Fucosidosis Alpha |
FUCA1 |
|
Gangliosidosis 1-3 |
GLB1 |
|
Globoid Cell Leukodystrophy 1, 2 |
GALC |
|
Glycogen Storage Disease IIIa 1 |
AGL |
|
Glycogen Storage Disease VII 1, 2 |
PFKM |
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Hereditary Methemoglobinemia 1, 2 |
CYB5R3 |
|
Hyperkeratosis |
FAM83G |
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Hypomyelination of Central Nervous System |
FNIP2 |
|
Hypophosphatasia |
ALPL |
|
Hypothyroidism 1-4 |
TPO |
|
Hypotrichosis 1, 2 |
SGK3 |
|
Ichthyosis 1-4 |
ASPRV1, PNPLA1, SLC27A4, TGM1 |
|
Intestinal Cobalamin Malabsorption |
AMN |
|
Junctional Epidermolysis Bullosa |
LAMA3 |
|
Lethal Acrodermatitis |
MKLN1 |
|
Leukodystrophy |
CYTB |
|
Ligneous Membranitis |
PLG |
|
Limb Girdle Muscular Dystrophy Type 2F |
SGCD |
|
Malignant Hyperthermia |
RYR1 |
|
Merle (Mc, Mc+, Ma, Ma+, M, Mh) |
PMEL |
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Mucopolysaccharidosis Type I 1 |
IDUA |
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Mucopolysaccharidosis Type VI 1, 2 |
ARSB |
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Mucopolysaccharidosis Type VII 1, 2 |
GUSB |
|
Muscular Dystrophy 1-8 |
COL6A1, DMD |
|
Muscular Hypertrophy |
MSTN |
|
Musladin Lueke Syndrome |
ADAMTSL2 |
|
Myotonia 1-3 |
CLCN1 |
|
Nasal Parakeratosis 1, 2 |
SUV39H2 |
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Nemaline Myopathy |
NEB |
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Oculocutaneous Albinism |
OCA2 |
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Oculocutaneous Albinism Type IV 1-3 |
SLC45A2 |
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Oculoskeletal Dysplasia 1, 2 |
COL9A2, COL9A3 |
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Osteochondrodysplasia |
SLC13A1 |
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Osteochondromatosis |
EXT2 |
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Osteogenesis Imperfecta 1-5 |
COL1A1, COL1A2, SERPINH1 |
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Palmoplantar Keratoderma |
KRT16 |
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Paroxysmal Dyskinesia |
PIGN |
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Periodic Fever Syndrome 1, 2 |
HAS2, MTBP |
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Persistant Mullerian Duct Syndrome |
AMHR2 |
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Pituitary Dwarfism |
LHX3 |
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Polyneuropathy 1-6 |
NDRG1, RAB3GAP1, ARHGEF10, GJA9 |
|
Pompe Disease |
GAA |
|
Pyruvate Dehydrogenase Deficiency |
PDP1 |
|
Pyruvate Kinase Deficiency of Erythrocyte 1-6 |
PKLR |
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Screw Tail |
DVL2 |
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Selective Cobalamin Malabsorption 1-3 |
CUBN |
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Spinal Dyraphism |
NKX2-8 |
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Spinocerebellar Ataxia 6 |
CAPN1 |
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Spondylocostal Dysostosis |
HES7 |
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Tail Length (TBXT) |
T (TBXT) |
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Van den Ende-Gupta Syndrome |
SCARF2 |
|
Vitamin D Deficiency Rickets Type II |
VDR |
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X-linked Hypohidrotic Ectodermal Dysplasia 1, 2 |
EDA |