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Dog DNA testing illustration

MDR1 Multi Drug Resistance – Dog

Kodas: H629

74,72 €

Mėginio duomenys

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Short description

Multi Drug Resistance 1 or Multidrug Sensitivity seems to inherited in an autosomal dominant way with incomplete penetrance.

General information

Multi Drug Resistance 1 or Multidrug Sensitivity seems to inherited in an autosomal dominant way with incomplete penetrance. Affected dogs are susceptible to neurotoxicity following the administration of certain commonly used drugs like Ivermectin. The condition is linked to the ATP Binding Cassette Subfamily B Member 1 (ABCB1) gene, also known as the multidrug resistance (MDR1) gene. This gene encodes for a drug transporter protein called P-glycoprotein (P-gp), which plays a crucial role in the blood-brain barrier by preventing certain drugs from accumulating in the brain. Dogs with two copies of the MDR1 variant are at higher risk and should be closely monitored to avoid adverse reactions to certain medications. Some dogs with one copy of the MDR1 variant have also been reported to exhibit multidrug sensitivity, though symptoms vary hugely.

Specifications

Breeds

Smooth Collie, Australian Shepherd, Border Collie, German Shepherd, Miniature American Shepherd, Old English Sheepdog, Rough Collie, Shetland Sheepdog, Whippet

Gene

ABCB1

Chromosome

14

Mutation

c.228_231del

Organ

Nervous System

Specimen

Swab, Blood EDTA, Blood Heparin, Semen, Tissue

Mode of Inheritance

Autosomal Dominant with Incomplete Penetrance

Also known as

MDR1

Clinical features

Neurotoxicity following drug administration, which varies according to dose, is the main sign. Dogs may show ataxia, tremors, seizures, excessive salivation, obtundation, bradycardia, mydriasis, loss of menace, loss of papillary light responses, coma and respiratory arrest.

Additional information

This test is based on an association study.

The disorder is noted as incomplete dominant. It means that, in some cases, carriers of the mutation have been observed to present with a milder form of the disorder and in other cases no symptoms were present at all.

References

Pubmed ID: 11692082

Year published: 2001

Omia ID: 1402

Omia variant ID:

Turnaround information

  • 10 working days