Cystinuria Labrador Retriever type (L-CYS)

54.90 € inc. Vat

Acronyms: IA Type Cystinuria, L-CYS
Gene: SLC3A1
Mutation: Deletion
Mode of inheritance: Autosomal recessive
Breeds: Labrador Retriever

Animal ID *

Name or unique identification of your animal microchip number, tattoo number, etc

SKU: CD112 Categories: , Tag:

Product Description

Cystinuria Labrador Retriever type (L-CYS)

Cystinuria Labrador Retriever type (L-CYS) is an inherited renal disorder affecting the Labrador retriever breed. Different forms of cystinuria have been identified in humans and in dogs, but also in several other carnivorous animal species, including mink, maned wolf and cat. The disorder has been most extensively studied in dogs. Cystinuria is considered a heterogeneous group of disorders, individually differing among each other in its severity and age of onset and first cystine stones formation. Other than that, cystinuria among dogs also differs in causative mutation and mode of inheritance. In humans, it is divided in two groups, type I and non-type I cystinuria. Studies have established that cystinuria affecting Newfoundland dogs shares many similarities with cystinuria type I in humans.

Characteristics and Symptoms

Cystinuria was one of the first identified inborn defects of metabolism. It was recognized by Sir Archibald Garrod as an inherited defect of renal transport that included malabsorption of cystine and the dibasic amino acids ornithine, lysine and arginine, collectively known as COLA. In dogs it has been reported for the first time in 1823 and today it is known to affect more than 70 dog breeds. In the normally functioning kidney, amino acids and some other substances are filtered out of the blood, and then reclaimed from the urine. Malabsorption of COLA amino acids in the proximal renal tubules causes their high concentrations in the urine of the affected individual. Main problems are caused by low solubility of cystine in urine of acidic and neutral pH. High concentrations of cystine in urine and its low solubility leads to cystine crystals and bladder stones formation, known as uroliths. Uroliths in the urinary tract can result in stranguria, hematuria, urinary obstruction and renal failure with possible fatal outcome.

Symptoms of disease include straining to urinate, frequent urination or inability to urinate. In Labrador retrievers both males and females are affected, but obstruction of urine flow is more common in males due to differences in anatomy and females tend to develop stones later than males. Dogs with cystinuria often have recurrent inflammation of the urinary tract and if not treated, urinary stones can cause urinary tract infections, kidney failure and even death.


Cystinuria Labrador Retriever type (L-CYS) is caused by a mutation SLC3A1 gene. SLC3A2 encodes for a transporter protein that allows the kidneys a transport of cystine and other amino acids from the urine. The mutation comprises a homozygous 1bp deletion in exon of the SLC3A1 gene. This deletion causes premature stop codon and consequently synthesis of defected protein, disabling COLA amino acids reabsorption to blood.

Cystinuria Labrador Retriever type (L-CYS) is inherited in an autosomal recessive manner. Healthy parents of an affected puppy are obligate heterozygotes, and therefore carry one mutant allele. Heterozygotes have no symptoms. Dogs homozygous for the mutation will display the symptoms of the L-CYS. At conception, when mating two carrier dogs, each cub has a 25% chance of being affected, a 50% chance of being an asymptomatic carrier, and a 25% chance of being unaffected and not a carrier.


Brons AK, Henthorn PS, Raj K, Fitzgerald CA, Liu J, Sewell AC, Giger U. SLC3A1 and SLC7A9 mutations in autosomal recessive and dominant canine cystinuria: A new classification system. J Vet Intern Med. 2013 Nov;27(6):1400-8.

Henthorn, P., Giger, U. (2003.): Challenges to understanding cystinuria in dogs that are not Newfoundlands.