Turnaround time
10 workdays
48.4
40
Genetic test for the SLC3A1 c.350delG variant that causes cystinuria type I-A and cystine stones in Labrador Retrievers.
Overview
This genetic test analyses the SLC3A1 variant c.350delG for cystinuria in Labrador Retriever dogs. Cystinuria is also described as cystine urolithiasis, cystine stones, cystine calculi, bladder stones or kidney stones. The test determines whether the dog is clear, heterozygous positive/carrier or homozygous positive/affected for this specific variant.
Cystinuria is an inherited metabolic disorder in which the kidneys fail to reabsorb cystine and related amino acids efficiently. As a result, too much cystine remains in the urine. Cystine is poorly soluble and can form crystals or stones in the bladder, urethra or kidneys.
The condition is also known as cystine urolithiasis, cystine stones, cystine calculi, bladder stones or kidney stones. Signs may include straining to urinate, frequent small urinations, blood in the urine, recurrent bladder inflammation and urinary obstruction. In male dogs, obstruction can become serious quickly because of the narrower urethra.
The trait is inherited as autosomal recessive. A dog with two normal alleles is clear. A dog with one copy is a carrier and can pass the variant on. A dog with two copies is genetically affected for this tested form of cystinuria.
Other causes can also produce urinary signs. This test therefore gives targeted genetic information about the variant for which the analysis was designed.
Included subanalyses
This analysis includes the following subanalysis:
Allele combinations & result interpretations
Below, for each tested locus, you will find the possible allele combinations that may be reported within this analysis, together with a brief explanation of their genetic meaning. The interpretation of possible interactions between different loci is included in the report, but is not shown here in full because that would lead to too many combinations on this page. The final expression may also depend on other genes and their interaction.
Genotype / allele combination: Clear / normal genotype (N/N)
The genotype N/N means the tested SLC3A1 variant c.350delG was not detected. This dog does not develop this variant-linked form of cystinuria and does not pass the tested variant on.
Genotype / allele combination: Carrier / one copy (N/del)
The genotype N/del means the dog carries one copy of the tested SLC3A1 variant c.350delG. One copy does not cause this autosomal recessive form, but the dog can pass the variant on. In breeding, combine only with a clear partner.
Genotype / allele combination: Affected / two copies (del/del)
The genotype del/del causes this tested form of cystinuria. The dog has two copies of the SLC3A1 variant c.350delG, is genetically affected and passes the variant to all offspring.
Sampling and submission guidelines





References