Turnaround time
10 workdays
48.4
40
DNA test for the KRT71 c.445-1G>C variant that causes the dominant Selkirk Rex curly coat.
Overview
This genetic test analyses the KRT71 variant c.445-1G>C, also known in the Selkirk Rex breed as SADRE, SLK or Re^S. KRT71 encodes keratin 71, a protein important for coat formation and structure.
The Selkirk Rex variant causes a dense, woolly, curly or tousled coat. One copy already gives a curly coat; cats with two copies can show a stronger or differently presented curl and body type.
The Selkirk Rex variant is autosomal incomplete dominant: one copy is visible, while two copies can further influence curl expression.
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: No Selkirk Rex curly coat variant
This cat does not carry the tested Re^S variant. It will not have Selkirk Rex curly coat due to this variant and will not pass it on.
Genotype / allele combination: One copy of Re^S
This cat has one copy of the Re^S variant. This causes Selkirk Rex curly coat and the variant can be passed to offspring.
Genotype / allele combination: Two copies of Re^S
This cat has two copies of the Re^S variant. This causes Selkirk Rex curly coat and can give a stronger or differently presented curl than one copy.
Sampling and submission guidelines





References