Turnaround time
10 workdays
48.4
40
Genetic test for the recessive ABCB1 c.1930_1931delTC variant that causes MDR1-related sensitivity to certain medicines in cats.
Overview
This genetic test examines the ABCB1 variant c.1930_1931delTC. The trait is also known as MDR1, Multi Drug Resistance 1, multidrug sensitivity, ivermectin sensitivity or P-glycoprotein deficiency. ABCB1 encodes P-glycoprotein, a transport protein that helps keep certain substances out of vulnerable tissues, including the central nervous system.
Cats with two copies of the variant produce insufficient functional P-glycoprotein. As a result, certain medicines, especially P-glycoprotein substrates such as macrocyclic lactones, can penetrate more strongly and cause more severe adverse effects. Neurological signs may include lethargy, ataxia, tremors, salivation, vomiting, dilated pupils, breathing problems, seizures, blindness, coma or death.
The result shows whether a cat carries zero, one or two copies of the tested ABCB1 variant. This helps owners, breeders and veterinarians make better informed medication and breeding decisions. For cats with two copies, the result is especially valuable because MDR1 status is relevant when using drugs that depend on P-glycoprotein transport.
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 ABCB1 variant was not detected. This cat is clear for this MDR1 variant and will not pass this variant to offspring.
Genotype / allele combination: Carrier
This cat has one copy of the tested ABCB1 variant. The cat is a carrier and can pass the variant on; this status is important for breeding plans and for keeping MDR1 information in the medical record.
Genotype / allele combination: Affected
This cat has two copies of the tested ABCB1 variant. This genotype causes MDR1-related P-glycoprotein deficiency and increases the risk of severe adverse effects with certain medicines.
Sampling and submission guidelines





References