DNA & genetic tests
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48.4

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40

Progressive retinal atrophy / rdAc-PRA / RD2 (CEP290-related) - Cat

DNA test for the CEP290 c.7584+9T>G variant that causes rdAc-PRA / retinal degeneration II in cats.

Turnaround time
10 workdays
test Methods
Sequencing
Test code
PVT-1629519E2C26
Species
Cat
Matrices
Blood, Blood (EDTA), Blood (Heparin), Swab, Tissue

Overview

rdAc-PRA / retinal degeneration II in cats

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.

How to read the result

  • Clear: the tested variant is not detected; the cat will not pass on this variant.
  • Carrier: the cat carries one copy; for recessive PRA forms, the cat remains clear because of this variant but can pass it on.
  • Affected: two copies cause this form of progressive retinal disease and provide clear breeding-risk information.

Practical value of this test

  • confirms whether a cat is clear, carrier or genetically affected for this specific variant;
  • identifies carriers reliably, even when they have normal vision;
  • supports breeding selection, mating plans and reducing affected offspring.

Included subanalyses

This analysis includes the following subanalysis:

  • Progressive retinal atrophy / rdAc-PRA / RD2 (CEP290)

Allele combinations & result interpretations

Sampling and submission guidelines

References