Korat GM1 Gangliosidosis

Quick Summary

Korat GM1 gangliosidosis causes progressive neurologic dysfunction and premature death in Korat cats.

Click here for Price and Turnaround Time

Phenotype: Korat GM1 gangliosidosis causes progressive neurologic dysfunction, including tremors, ataxia, and dysmetria. Disease onset begins around 3 months of age and reaches terminal stage around 9-10 months, at which point blindness and epileptiform seizures are also observed.

Mode of Inheritance: Autosomal recessive

Alleles: N = Normal, GM1k = Korat GM1 gangliosidosis

Breeds appropriate for testing: Korat, Siamese

Explanation of Results:

  • Cats with N/N genotype will not have Korat GM1 gangliosidosis and cannot transmit this GM1 variant to their offspring.
  • Cats with N/GM1k genotype will not have Korat GM1 gangliosidosis, but are carriers. They will transmit this GM1 variant to 50% of their offspring. Matings between two carriers are predicted to produce 25% kittens with Korat GM1 gangliosidosis.
  • Cats with GM1k/GM1k genotype will have Korat GM1 gangliosidosis, a fatal condition.

Turnaround Time
At least 15 business days; may be delayed beyond 15 business days if sample requires additional testing, or a new sample is requested.
Price

$44 one test per animal
$66 this test + Korat GM2 per animal

Cat DNA tests are carried out using cells brushed from your cat's cheeks and gums using household cotton swabs.

The cat DNA submission form with instructions and a place to tape the cotton swabs is sent to you via email after you place an order, and can be printed from your home computer. DNA test kits are no longer mailed.

Instructions

Step-By-Step:

1.

Person looking at different brands of cotton swabs in a storePurchase regular household cotton swabs for cat DNA collection (the cotton swabs can be purchased at a pharmacy or drug store)

 

 

 

 

2.

Three Bengal kittens

Make sure the cat has not had anything to eat or drink for at least 1 hour prior to collecting sample.
When swabbing kittens, isolate each kitten from the mother, littermates and any shared toys for 1 hour prior to swabbing. Kittens should not have nursed or eaten for 1 hour prior to collecting sample.

If collecting samples from more than one cat, make sure to sample one cat at a time and wash your hands before swabbing another cat.

 

 

3.

Label indicating both ends of the two cotton swabs Use both ends of the two cotton swabs for a total of four swabs.

 

 

 

 

 

4.

Place the cotton head of the swab between the cat’s gums and cheek and rub or rotate the swab back and forth for 15 seconds. Repeat with each cotton swab head, for a total of 4 swabs. We recommend swabbing a different area of the gums with each swab head.

 

 

5.

Wave the swab in the air for 10-15 seconds to air dry it before attaching it to the submission form.

 

6.

Cotton swabs taped to bar-coded submission form for VGLAfter swabbing the cheek and gums, tape the cotton swabs to the bar-coded submission form printed from your MyVGL account.

 

ATTENTION:

  • Do not collect saliva/drool – the key to obtaining a good sample is getting cheek cells on the swab.
  • Do not rub swab on the cat’s tongue or teeth – this will result in poor quality sample.
  • Do not collect a sample from a kitten that has recently nursed – the mother’s genetic material can rub off on the kitten’s mouth and contaminate the sample.
Additional Details

Gangliosidoses are degenerative, fatal neurological diseases caused by abnormal accumulation of lipids known as gangliosides in central and peripheral nervous systems, and nerve cells in particular. Cats affected with gangliosidosis have progressive neurologic dysfunction and premature death. Two forms of gangliosidosis affect Korat cats – GM1 and GM2. Both have a genetic basis and a recessive mode of inheritance. Two copies of the defective gene are needed to cause the disease. Both diseases cause similar progressive neurologic dysfunction, including tremors, ataxia, and dysmetria. Disease progression is more rapid in GM2.

Korat GM1 is caused by a mutation in exon 14 of the Beta-Galactosidase gene (GLB1). Disease onset begins around 3 months of age and reaches terminal stage around 9-10 months, at which point blindness and epileptiform seizures are also observed. The mutation has been found in the Siamese breed which was used in the development of the Korat breed.

Testing for GM1 and GM2 in Korat cats assists owners and breeders in identifying affected and carrier cats. Breeders can use these tests as a tool to avoid breeding carriers together which would produce 25% affected offspring.

 

Note: This test is specific for the single base substitution in the GLB1 gene that causes GM1 in Korat and Siamese cats. It will not detect other gangliosidosis mutations known to exist in other breeds of cats.