Turnaround time
10 workdays
48.4
40
DNA test for the CEP290 c.7584+9T>G variant that causes rdAc-PRA / retinal degeneration II in cats.
Overview
This DNA test assesses the CEP290 variant c.7584+9T>G that causes rdAc-PRA / retinal degeneration II. The disorder is also known as rdAc, PRA-CEP290, PRA-B, retinal degeneration II, RD2, late-onset photoreceptor degeneration and progressive retinal atrophy. Progressive retinal atrophy is an inherited retinal disorder in which light-sensitive cells gradually lose function.
Cats with this form are usually born with normal vision. Vision can then decline gradually; many affected cats develop progressive blindness between about three and five years of age, although progression can differ between animals.
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
The tested variant for rdAc-PRA / retinal degeneration II was not detected. This cat is clear for this variant and will not pass it on.
Genotype / allele combination: Carrier
The cat carries one copy of the tested variant for rdAc-PRA / retinal degeneration II. The cat is a carrier and can pass this variant to offspring.
Genotype / allele combination: Affected
The cat has two copies of the tested variant. This genotype causes rdAc-PRA / retinal degeneration II and is important for breeding plans and follow-up.
Sampling and submission guidelines





References