Turnaround time
10 workdays
48.4
40
DNA test for the RETN c.19C>T variant interpreted as a copper toxicosis modifier in Labrador Retrievers.
Overview
This genetic test analyses the RETN c.19C>T variant in Labrador Retriever. The disorder and risk profile are described as copper toxicosis, copper storage disease, copper accumulation, copper-associated hepatopathy and copper-associated chronic hepatitis. This test analyses a RETN variant used as a copper toxicosis modifier in Labrador Retrievers. The variant has been linked to lower hepatic copper values in research, but is most useful when interpreted together with ATP7A and ATP7B.
Copper is required for normal metabolism, but excess copper in the liver damages liver cells. Dogs with copper toxicosis can appear normal for a long time and later develop increased liver enzymes, poor appetite, vomiting, lethargy, weight loss, jaundice, behavioural change, chronic hepatitis or liver cirrhosis. Diet, other genetic factors and breed background all influence how strongly the genotype is expressed.
RETN does not follow a classic Mendelian disease inheritance pattern here. The test is used as modifier information: one or two copies can influence the copper profile, especially together with ATP7B and ATP7A.
This DNA test is practically useful because copper accumulation often becomes visible only late. An early genetic result helps breeders avoid risk matings, helps owners understand which dogs deserve extra attention and supports more targeted follow-up when liver values or family history make that relevant.
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 RETN variant detected (C/C)
The RETN c.19C>T variant was not detected. This result does not provide a RETN modifier profile; assess copper risk together with the other relevant copper metabolism tests.
Genotype / allele combination: One RETN variant copy (C/T)
The dog carries one copy of the RETN variant. This can influence the copper profile, but is most useful when interpreted together with ATP7B and ATP7A.
Genotype / allele combination: Two RETN variant copies (T/T)
The dog has two copies of the RETN variant. This gives the highest RETN modifier dose and is mainly useful for combined copper toxicosis interpretation in Labrador Retrievers.
Sampling and submission guidelines





References