Latest News

New Test Available - Cerebellar Ataxia (CA) in the Spinone Italiano

Spinocerebellar ataxia (also known as cerebellar ataxia or CA) is an inherited disorder that affects the Spinone Italiano and is characterized by early onset of progressive incoordination (ataxia). Affected dogs are normal at birth and begin showing signs of incoordination and loss of balance at about 4 months of age. The disorder progresses with clinical signs worsening in the next few months. Affected puppies are often euthanized before they reach one year of age due to the inability to ambulate and poor quality of life.

VGL parentage testing confirms rare event in equine reproduction

Delayed embryo development is a rare occurrence in horses. In collaboration with researchers at Colorado State University, results from UC Davis VGL parentage testing verified this rare finding in a donor Quarter Horse (QH) mare. 

New Test Available - Primary Open-Angle Glaucoma (POAG) in the Petit Basset Griffon Vendeen

Primary open-angle glaucoma (POAG) is a type of glaucoma that typically progresses gradually and without obvious signs of pain. A genetic inversion disrupting the ADAMTS17 gene is associated with POAG in the Petit Basset Griffon Vendeen. POAG is characterized by elevated intraocular pressure (increased pressure inside the eye) and partial dislocation of the lens.

New Test Available 🧬🐶 - GM2 Gangliosidosis in the Toy Poodle

GM2 gangliosidosis is a fatal neurodegenerative lysosomal storage disease that affects dogs. A genetic variant causing GM2 gangliosidosis has been identified in certain lineages of Toy Poodles.

Affected dogs typically display neurological signs that begin at 9-12 months of age and may include tremor, incoordination or stiff gait, and difficulty eating. Neurological deterioration progresses over 6-12 months, ultimately resulting in death.

Test Update: new W13 allele added to VGL’s equine Dominant White test

The equine Dominant White test offered by the VGL has been updated to include a fifth allele: W13. This KIT mutation consists of a single base substitution and was initially identified in a Quarter Horse X Paso Peruano cross-bred family that had two white horses.

Announcement: VGL’s Cat Ancestry Test will be discontinued as of December 16

The VGL’s cat ancestry test was developed to determine which geographic region a random bred cat has originated from: Western Europe, Egypt, East Mediterranean, Iran/Iraq, Arabian Sea, India, South Asia and East Asia. It was not designed to answer the question, what is the breed composition of my cat? As such, the results that we are scientifically able to provide with this DNA test are not able to answer the question some of our clients have. Therefore, we have decided to discontinue the offering of this test effective December 16, 2022.

New American Quarter Horse Association Online Educational Resource for Equine Genetic Health

Understanding the results of genetic testing and how to best utilize them is an important component for advancing the health of animals. The American Quarter Horse Association (AQHA) recently formed a task force consisting of veterinarians, geneticists, AQHA staff and AQHA members, to assist in the development of an online resource to aid in the understanding and utilization of the results of genetic testing performed by the UC Davis Veterinary Genetics Laboratory (VGL). 

AQHA has added MYHM to the American Quarter Horse Genetic Health Panel offered through the Association

The American Quarter Horse Association (AQHA) has just announced that the myosin-heavy chain myopathy (MYHM) test has been added to the American Quarter Horse Genetic Health Panel offered through the Association. The decision to add MYHM was made earlier this year at the 2022 AQHA Convention in Las Vegas, NV, following a rule-change proposal submitted by an AQHA member. Starting December 1st, 2022, MYHM will be automatically included in the health panel test ordered through AQHA.

How genetic testing for MYHM helped Legend, a six year old American Quarter Horse

Legend, a 6-year-old American Quarter Horse, was showing signs of lethargy, loss of appetite, fever, dark urine, edema and muscle loss in the hindquarters. Soon after noticing a change in her horse, the concerned owner, Karissa Waber, decided to take him to her veterinarian for care. Legend was hospitalized for 8 days, but despite this care, his condition continued to worsen. In only a few days he developed colitis and signs of kidney failure. Nonetheless, Karissa’s veterinarian, Dr. Mem Dailey, was not ready to give up on Legend and started him on steroid treatments.

Variants associated with equine familial isolated hypoparathyroidism (EFIH) and fragile foal syndrome (FFS) are at low frequency in the US Thoroughbred population and are not recent mutations

The study led by Dr. Carrie Finno, Gregory L. Ferraro Endowed Director of the UC Davis Center for Equine Health (CEH), and Dr. Rebecca Bellone, Director of the Veterinary Genetics Laboratory (VGL), determined that the allele frequencies for equine familial isolated hypoparathyroidism (EFIH) and fragile foal syndrome (FFS) were low in a population of Thoroughbred horses.

New Test Available: Progressive Retinal Atrophy (rcd4-PRA)

Progressive retinal atrophy (PRA) is a term used to describe a group of inherited disorders of the retina, characterized by progressive retinal degeneration and consequent blindness. More than 20 mutations in various genes have been associated with PRA in dogs.

VGL Research identify risk factors for insidious uveitis in Knabstrupper horses

A study conducted by an international team of researchers led by VGL director, Dr. Rebecca Bellone, and with research performed by recent VGL Ph.D. recipient Nicole Kingsley, found that age and homozygosity for the leopard complex spotting allele (LP) are risk factors for insidious uveitis in the Knabstrupper horse. Genotyping for LP is, therefore, useful to assess risk and help inform clinical evaluations of equine recurrent uveitis in this breed.

VGL collaborative research investigates the prevalence of known genetic variants in horses with muscle disease

A collaborative study between the Neuromuscular Disease Laboratory and the Veterinary Genetics Laboratory at the University of California, Davis, showed that genetic variants known to cause skeletal muscle disorders were present in one third of horses with clinical diagnosis of muscle disease who were submitted for histopathological examination.

Dr. Aleman, Professor in the Department of Medicine and Epidemiology at UC Davis, an expert in neuromuscular biology and lead investigator of this study noted: