|
Gene/Disease |
Comments |
Laboratory |
|
Alpha-mannosidosis (MA) |
Cattle |
|
|
Arthrogryposis
multiplex |
Cattle |
|
|
Blood typing in
macaques |
Identification of blood type in cynomolgus and rhesus macaques - blood group A, B or AB |
|
|
Blood typing in
pigs |
Identification of blood type in swine - blood
group AA, AO or OO. |
|
|
Cerebellar Abiotrophy Screening Test (CA) |
Arabian horses |
|
|
Chondrodysplasia
(CHO) |
Cattle |
|
|
Congenital
Stationary Night Blindness (CSNB) |
Appaloosa |
|
|
Contractural Arachnodactyly (CA) |
Cattle |
|
|
Detection and
differentiation of rhesus and cynomolgus macaque
DNA |
Identification of full-blooded rhesus,
full-blooded cyno, or hybrid. |
|
|
Developmental
Duplication (DD) |
Cattle |
|
|
Dexter Bulldog
Dwarfism (Chondrodysplasia) |
Cattle |
|
|
Dexter
Pulmonary Hypoplasia with Anasarca (PHA) |
Cattle |
|
|
Digital
Subluxation (DS) |
Cattle |
|
|
Foal Immunodeficiency
Syndrome |
Sodium/myo-inositol
cotransporter gene (SLC5A3) mutation |
|
|
Freemartin |
|
|
|
G6-Sulfatase
Deficiency (G6-S MPSIIID) |
Nubian goats |
|
|
Genotyping of cynomolgus DNA by PCR fragment analysis |
This assay identifies genetic origin of a cynomolgus macaque sample by microsatellite marker
analysis. It uses five Macaca fascicularis genomic markers to determine the
relatedness of two animals, or to attribute a sample to a source animal. |
|
|
Glycogen
Branching Enzyme Deficiency (GBED) |
Quarter Horses |
|
|
Hereditary
Equine Regional Dermal Asthenia (HERDA) |
|
|
|
Hoof Wall
Separation Disease |
Connemara Pony |
|
|
Hydrocephalus
in Friesian horses |
Nonsense mutation in B3GALNT2 |
|
|
Hyperkalemic
Periodic Paralysis (HYPP) |
|
|
|
Hypotrychosis (HY) |
Cattle |
|
|
Idiopathic
Epilepsy |
Cattle |
|
|
Junctional
Epidermolysis Bullosa (JEB) |
Belgian Draft horses, American Saddlebred |
|
|
Karyotyping |
|
|
|
Lavender foal
syndrome |
Arabian horses |
|
|
Lethal White
Foal Syndrome |
American Paint (overo) |
|
|
Malignant
Hyperthermia (MH) |
|
|
|
Mamu-6 in
macaques |
|
|
|
Mamu-7 in
macaques |
|
|
|
Myostatin |
Cattle |
|
|
Neuropathic
hydrocephalus |
Cattle |
|
|
Osteopetrosis |
Cattle |
|
|
Polysaccharide
storage myopathy- type I |
Quarter Horses |
|
|
Scrapie
susceptibility |
|
|
|
Severe combined
immunodeficiency (SCID) |
Arabian foals |
|
|
Spider lamb |
|
|
|
Splashed White
Overo (SW-1, SW-2, SW-3) |
|
|
|
Tibial Hemimelia |
Cattle |
|
|
Warmblood
Fragile Foal Syndrome |
Mutation in lysyl
hydroxylase 1 (LHl) gene |
