Turnaround time
10 workdays
48.4
40
DNA test for ACSL5-related intestinal lipid malabsorption / ILM in Australian Kelpies, analysing the g.23380074_23483377del deletion.
Overview
This genetic test analyses the ACSL5 deletion g.23380074_23483377del for intestinal lipid malabsorption in the Australian Kelpie. The condition is also known as ILM, lipid malabsorption, dietary fat malabsorption, fat malabsorption and ACSL5-related metabolic disorder. The test shows whether the dog is clear, a carrier or has two copies of the tested deletion.
ACSL5 is involved in processing and absorption of long-chain fatty acids in the intestine. Puppies with two copies of the deletion absorb dietary fat inefficiently, even when food intake is normal or increased. This can lead to poor growth, smaller size compared with littermates and abnormal faeces.
Typical signs include failure to thrive, polyphagia, pale or fatty faeces, steatorrhea, abdominal distension, increased faecal volume and a dull or wiry coat. Signs can improve with age, but affected dogs can remain smaller and less tolerant of high-fat diets.
The test is especially valuable for Kelpie breeders, owners of related lines and veterinarians who want to place digestive or growth problems in a young Kelpie in a genetic context. An early result makes breeding plans, puppy-buyer communication and practical dietary choices much clearer.
ILM is inherited as autosomal recessive. N/N means that the tested deletion was not detected. N/del means that the dog is a carrier and can pass the deletion on. del/del causes the tested form of intestinal lipid malabsorption.
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 variant detected (N/N)
The tested ACSL5 deletion was not detected. This dog will not pass this specific ILM deletion to offspring.
Genotype / allele combination: One variant copy detected (N/del)
The dog carries one copy of the tested ACSL5 deletion. The dog can pass the deletion on; matings with another carrier create a risk of puppies with intestinal lipid malabsorption.
Genotype / allele combination: Two variant copies detected (del/del)
The dog has two copies of the tested ACSL5 deletion. This genotype causes the tested autosomal recessive form of intestinal lipid malabsorption.
Sampling and submission guidelines





References