Turnaround time
10 workdays
48.4
40
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.
Overview
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.
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.
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:
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 / normal genotype (N/N)
The dog does not carry the tested ENAM variant for amelogenesis imperfecta / FEH. This animal will not pass this specific variant to offspring.
Genotype / allele combination: Carrier (N/delTTTCC)
The dog carries one copy of the tested ENAM variant. Carriers generally do not develop this recessive form themselves, but can pass the variant on; two carriers together can produce affected puppies.
Genotype / allele combination: Genetically affected (delTTTCC/delTTTCC)
The dog has two copies of the tested ENAM variant. This genotype causes the recessive form of amelogenesis imperfecta / FEH covered by this test and explains the genetic risk of abnormal dental enamel.
Sampling and submission guidelines





References