Turnaround time
10 workdays
48.4
40
DNA test for the SLC5A3 c.1337G>T variant that causes Foal Immunodeficiency Syndrome in Fell and Dales ponies.
Overview
This genetic test detects the SLC5A3 variant c.1337G>T that causes Foal Immunodeficiency Syndrome, abbreviated FIS, in Fell and Dales ponies. The disorder is a severe inherited immunodeficiency of foals.
Affected foals often appear normal at birth but usually develop progressive anemia and recurrent infections during the first weeks of life. Typical signs include weakness, poor growth, diarrhea, coughing, respiratory problems, failure to suckle properly and reduced immune protection.
FIS is inherited as an autosomal recessive disorder. This test is highly valuable for breeding decisions: identifying carriers makes it possible to avoid carrier-to-carrier matings while still using valuable carriers responsibly when paired with clear animals.
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 (GG)
The tested horse does not carry the assessed variant for Foal Immunodeficiency Syndrome. It will not develop this autosomal recessive disorder due to this variant and will not pass this variant to offspring.
Genotype / allele combination: Carrier / one copy (GT)
The tested horse carries one copy of the assessed variant. The animal is a carrier and is generally not affected by one copy, but can pass the variant to about half of its offspring. Mating two carriers can produce affected foals.
Genotype / allele combination: Affected / two copies (TT)
This horse has two copies of the SLC5A3 c.1337G>T variant. This genotype causes Foal Immunodeficiency Syndrome; affected foals develop severe immunodeficiency and usually die young or require euthanasia.
Sampling and submission guidelines







References