DNA & genetic tests
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Amelogenesis imperfecta / FEH (ENAM-related) - Greyhound / Italian Greyhound

DNA test for the ENAM c.1991_1995delTTTCC variant that causes inherited amelogenesis imperfecta, also called AI or familial enamel hypoplasia, in Greyhounds and Italian Greyhounds.

Turnaround time
10 workdays
test Methods
Sequencing
Test code
PVT-CAD8CB2B6987
Species
Dog
Breeds
Greyhound, Italian Greyhound
Matrices
Blood, Blood (EDTA), Blood (Heparin), Swab, Tissue

Overview

What does this test examine?

This genetic test examines the ENAM c.1991_1995delTTTCC variant in Greyhounds and Italian Greyhounds. The condition is known as amelogenesis imperfecta, AI, familial enamel hypoplasia or FEH. This variant affects the formation and quality of dental enamel.

What does this mean for the dog?

Amelogenesis imperfecta disrupts enamel development in deciduous and permanent teeth. Affected dogs can develop thin, rough or irregular enamel, often with brown discoloration, pitting, faster wear and small or pointed teeth. As a result, the teeth are more vulnerable and dental care can become important from a young age.

Practical value of this test

  • The test shows whether the dog is clear, a carrier or has two copies of the tested variant.
  • Breeders can manage carriers deliberately and avoid pairings that may produce affected puppies.
  • In young dogs, the result helps explain tooth changes genetically and supports a more informed breeding plan.

The condition is inherited as an autosomal recessive trait. Carriers have one copy of the variant and pass it to some offspring; dogs with two copies develop the genetic presentation of ENAM-related amelogenesis imperfecta.

Included subanalyses

This analysis includes the following subanalysis:

  • Amelogenesis imperfecta / FEH (ENAM, Greyhound type)

Allele combinations & result interpretations

Sampling and submission guidelines

References