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by Blitzen on 08 July 2015 - 15:07
IMO the dog should be DNA tested for DM and if found to be at risk autopsied when the time comes. The results should not be used to dictate treatment or to make a positve DM diagnosis. How else can the researchers prove or disprove the test results? It should be about the breed not who is right and who is wrong. Hasn't that attitude gone on long enough and how has it worked for the breed so far?
by Blitzen on 08 July 2015 - 15:07
"Neurologist said DNA testing would just show if he was a carrier and at this point I don't see any reason to do it."
That was the reason for not DNA testing Stuart ^^^^.
Breeders selling "dm free" dogs are no more dishonest that those who sell dogs based on overstated show results, working ability, progeny evaluation, and other BS. What's the difference?
by Villa Maximus on 08 July 2015 - 20:07
Can someone assist in explaining what they believe the following might mean for my seemingly healthy and active 3-year old GSD? Will he develop DM symptoms? Likelihood of developing symptoms? If I mate him with a dog 100% free and clear of the DM gene are they still within the 50 percentile of getting the gene? He is a wonderful dog. Sire was VA1 in Germany a few years ago as was grand-sire. Hips and elbows are completely normal (A-). Thoughts?
LABOKLIN GmbH&CoKG
Steubenstraβe 4
DE-97688 Bad Kissingen
Fax-Nr.: +49 971 68546
Tel.: +49 971 72020
Report
No.: ---
Date of arrival: 24-12-2014
Date of report: 29-12-2014
+----------------------------------------------------------------+
| Patient identification: Dog Male * 19.02.12 |
| German Shepherd Dog |
| Owner / Animal-ID: --- |
| Type of sample: EDTA-Blood |
| Date sample was taken: 12-12-2014 |
+----------------------------------------------------------------+
Name: ---
Stud book no.: ---
Chip no.: ---
Tattoo no.: ---
Degenerative Myelopathy - PCR
Result: genotype N/DM (exon 2)
Interpretation: The analysed dog is a carrier of the mutation in exon 2 of SOD1-gene that has been suggested to be a major risk factor for the development of Degenerative Myelopathy. The mutation will be passed on to the offspring with a probability of 50%.
Please note: In the Bernese Mountain Dog breed the mutation in exon 1 of SOD1 gene also occurs in correlation with DM.
The current result is only valid for the sample submitted to our laboratory. The sender is responsible for the correct information regarding the sample material.The laboratory can not be made liable. Furthermore, any obligation for compensation is limited to the value of the tests performed.
There is a possibility that other mutations may have caused the disease/phenotype. The analysis was performed according to the latest knowledge and technology.
The laboratory is accredited for the performed tests according to DIN EN ISO 17025 (D-PL-13186-01). (except partner lab tests).
*** END of report ***
Fr.Dipl.-Biol. Bärbel Gunreben
Abt. Molekularbiologie
by Blitzen on 08 July 2015 - 20:07
Villa, this might help you make a decision.
http://www.caninegeneticdiseases.net/DM/testDM.htm
by joanro on 08 July 2015 - 21:07
"There is a possibility that other mutations may have caused the disease/phenotype. The analysis was performed according to the latest knowledge and technology."
by joanro on 08 July 2015 - 21:07
"Interpretation: The analysed dog is a carrier of the mutation in exon 2 of SOD1-gene that has been SUGGESTED to be a major risk factor for the development of Degenerative Myelopathy."
Looks to me like this lab is doing a courtesy by testing for the sod1 gene, but doesn't believe in the validity of the test.
by Blitzen on 08 July 2015 - 22:07
Joan, did you read the link I posted here?
by Blitzen on 08 July 2015 - 22:07
Villa, read all the available information on DM and decide for yourself how you use the results.
by Blitzen on 08 July 2015 - 22:07
What do you in the US who follow the German guidelines intend to do should the SV require a DM DNA test prior to breeding? That could happen you know.
by Blitzen on 08 July 2015 - 22:07
Looks to me like this lab is doing a courtesy by testing for the sod1 gene, but doesn't believe in the validity of the test.
How did you decide that, Joan?
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