Archives for October 2019

As part of our commitment to raising the standard in canine genetic disease testing, the team at Paw Print Genetics works hard to assess the validity of genetic mutations published in the medical literature and to develop new disease tests based upon this information. The most recent test to be added to our extensive disease testing menu is for a disease known to be inherited in golden retrievers called   neuronal ceroid lipofuscinosis 5.

What is neuronal ceroid lipofuscinosis 5?

Neuronal ceroid lipofuscinosis (NCL) is an inherited neurological disease belonging to a group of diseases called lysosomal storage diseases. There are multiple types of NCL, each given a number designation based upon the specific gene in which the associated genetic mutation is found. For example, dogs diagnosed with neuronal ceroid lipofuscinosis 5 (NCL5) have inherited a genetic mutation in the canine CLN5 gene. Although there are multiple dog breeds known to inherit NCL5 due to mutations in this gene, the specific mutation responsible for this disease in golden retrievers has only been found in this breed; thus, making testing for NCL5 in golden retrievers breed-specific.

What do the symptoms include?

Dogs affected with NCL5 are born with a deficiency of a ...

Over the past two decades, usage of genetic testing technologies has revolutionized the world of dog breeding. Once limited to selective breeding practices based upon the characteristics or disease states that could be physically observed in a dog, genetic testing has allowed dog breeders to uncover the inherited genetic variants (mutations) that are not being expressed in an individual but may be expressed in their offspring. By comparing the disease-associated mutations inherited by a dog to those of a prospective mate, informed breeding decisions can be made to avoid producing puppies with these diseases. However, despite the immense value of genetic disease testing in the production of healthy puppies, incorrect assumptions about the parentage of a litter can have disastrous consequences for the health of a kennel, even when parental genetic disease testing results are 100% accurate.

Clear by Parentage/Hereditary Clear

In ideal situations, potential dams and sires are tested for breed-specific, disease-associated genetic mutations prior to being bred. If both parents are found to be free of these mutations (often referred to as being “clear”), it can be assumed for practical purposes that the offspring are also clear of the same mutations. With this understanding, it is common ...