Turnaround time
10 workdays
48.4
40
Genetic test for the dominant FLCN c.764A>G variant in renal cystadenocarcinoma and nodular dermatofibrosis (RCND) in the German Shepherd Dog.
Overview
This genetic test examines the FLCN variant c.764A>G in the German Shepherd Dog. The variant is associated with renal cystadenocarcinoma and nodular dermatofibrosis, commonly abbreviated as RCND. The disorder is also described as renal cancer syndrome, nodular dermatofibrosis and kidney disease, or hereditary multifocal renal cystadenocarcinomas with skin nodules.
RCND is an inherited cancer syndrome in which dogs can develop firm skin nodules and cystic or tumour-like lesions in the kidneys. Female dogs may also develop uterine leiomyomas. The condition is progressive and often becomes visible later in life, so genetic information is valuable before clinical signs are obvious.
Because the disorder is autosomal dominant, one copy of the tested variant is already important for breeding selection and health planning. The test helps identify risk in a line early, instead of waiting until skin nodules or kidney problems become visible.
A dog with A/A does not carry the tested variant. A dog with A/G carries one copy of the dominant variant and has genetic predisposition for RCND. A dog with G/G carries two copies of the variant; this is a clearly abnormal result that should be considered very significant within the dominant disease model.
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: A/A - variant not detected
This dog does not carry the tested FLCN variant and will not pass this variant to offspring.
Genotype / allele combination: A/G - dominant variant present
This dog carries one copy of the dominant FLCN variant. This genotype causes genetic predisposition for RCND and the variant can be passed to about half of the offspring.
Genotype / allele combination: G/G - two copies of the dominant variant
This dog carries two copies of the FLCN variant. In this dominant disease model, presence of the variant means genetic predisposition for RCND; this result is therefore highly relevant for breeding selection and follow-up.
Sampling and submission guidelines





References