Turnaround time
10 workdays
48.4
40
DNA test for the WNK4 c.2899C>T variant that causes Burmese hypokalaemic periodic paralysis/BHP in cats.
Overview
This genetic test analyses the WNK4 variant c.2899C>T that causes hypokalaemic periodic paralysis in cats. The condition is also known as Burmese Hypokalemia, BHP, HPP or feline hypokalaemic periodic paralysis.
Affected cats develop abnormally low blood potassium with episodes of muscle weakness. This can appear as weakness of the neck and head muscles, head bobbing, muscle tremors, a short gait, difficulty moving and sometimes generalized weakness.
The condition is autosomal recessive: cats with two copies of the variant are genetically affected, while carriers can pass the variant on.
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 for the WNK4 variant
This cat carries no copy of the tested WNK4 variant. It will not develop Burmese Hypokalemia/BHP due to this variant and will not pass it on.
Genotype / allele combination: Carrier of the WNK4 variant
This cat carries one copy of the tested WNK4 variant. It is not expected to be affected, but can pass the variant to offspring.
Genotype / allele combination: Genetically affected for Burmese Hypokalemia/BHP
This cat has two copies of the tested WNK4 variant. This genotype causes Burmese Hypokalemia/BHP with risk of episodes of muscle weakness due to low potassium levels.
Sampling and submission guidelines





References