Turnaround time
10 workdays
48.4
40
DNA test for the FAM8A1 c.485_507del variant that causes REM sleep behaviour disorder / RBD in Russian Blue cats.
Overview
This genetic test detects the FAM8A1 c.485_507del deletion that causes REM sleep behaviour disorder (RBD) in Russian Blue cats. The condition is also described as hereditary encephalopathy and can involve abnormal movements during REM sleep, vocalisation, sudden jerking or jumping, and impaired bladder control.
Affected cats may show episodes in which the normal muscle inhibition during sleep is disturbed. In the described Russian Blue families, urinary retention, overflow incontinence and sometimes dilated pupils were also reported. The severity and frequency of episodes can vary between cats and may increase over time.
RBD caused by this FAM8A1 variant follows an autosomal recessive inheritance pattern. The test helps breeders identify carriers, plan matings more confidently and avoid affected kittens.
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 / no tested variant
This genotype contains no copy of the tested variant. The cat will not develop REM sleep behaviour disorder caused by this FAM8A1 variant due to this variant and will not pass this variant to offspring.
Genotype / allele combination: Carrier / one copy
This genotype contains one copy of the tested variant. With autosomal recessive inheritance, one copy does not cause REM sleep behaviour disorder caused by this FAM8A1 variant, but the cat can pass the variant to offspring. Mate carriers only to animals tested clear.
Genotype / allele combination: Affected / two copies
This genotype contains two copies of the tested variant. This causes REM sleep behaviour disorder caused by this FAM8A1 variant; the animal will pass the variant to all offspring.
Sampling and submission guidelines





References