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CH Outlaws Sure Hit “Jonah”
Jennifer & Mirko WalterKreuzbergstr.44 | 47800 Krefeld | NRW | Germany
CH Outlaws Sure Hit “Jonah”
CH Outlaws Sure Hit “Jonah”
Hip / Ellbow (HD & ED)
OR
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DNA
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s be
en v
erifi
ed a
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the
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atab
ase.
havi
ng fu
lly c
ompl
eted
the
requ
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ents
of t
his
club
On
this
dat
e A
pril
12,
2015
OW
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RSH
ER
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SA
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Mar
ch 2
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Issu
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ASC
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RflPD VPN BEHEERD U T C H K E N N E L CL UB
Canine DNA ISAG2006 certificate
Name:NHSB number: BreedDate of birth:Microchipnumber:Sex:VHL-id:
OUTLAWS SURE HIT N.H.S.B. 3014396 DE AUSTRALIAN SHEPHERD 28/02/2012 981020013491908 MALE H l14931
Printdate: 6 Oktober 2015 at the Raad van Beheer in Amsterdam
The DNA profile is in compliance with the International Standard ISAG2006:
AHT121 100/108 INU030 144/150AHT137 137/137 INU055 210/210AHTH171 221/233 REN162C04 202/202AHTH260 238/240 REN169D01 210/212AHTK211 87/89 REN169018 164/166AHTK253 288/292 REN247M23 268/268CXX279 120/124 REN54P11 222/226FH2054 152/152 AHTH130 125/125FH2848 238/244 AMELOGENIN 182/217INRA21 99/101 REN64E19 147/153INU005 124/124 REN105L03 241/241
This DNA test is available at Certagen GmbH (part of Van Haeringen Group- VHL), and commissioned by the Dutch Kennel Club 'Raad van Beheer'. VHL exercises the utmost care in performing and/or registering each DNA test. No party other than the dient may derive any rights from the results of this DNA test. The General Terms of Delivery of the Dutch Kennel Club 'Raad van Beheer' apply to this DNA test.
This certificate is an integral part of the pedigree issued by the Dutch Kennel Club 'Raad van Beheer'.
In Cooperation with Van Haeringen Group.
AMERICAN KENNEL CLUB
' N ^ oeo
May 11,2016
R AGTERBERG-MENNES VLEDDERHUIZEN 3 9591 TK ONSTWEDDE NETHERLANDS
Letter of DNA AnalysisBfeed: Australian Shepherd DNA Profile #GV784949^Sex: MaleDate o f Birth: 28-FEB-2012 ID # : 981020013491908 Date o f Analysis: 21-APR-2016 AKC #: DN34605901 AKC Name: Outlaws Sure Hit Owner(s): Ragterberg Mennes
The following genotype uniquely represents the Neogen Corporation genetic identity of the dog named herein:
Neogen#: C0928410
D D A G A A C F A D F F D D B D B B A C F G D D C F X YPEZ 1 PEZ 3 PEZ 5 PEZ 6 PEZ 8 PEZ 12 PEZ 20 UCB 2010 UCB 2054 UCB 2079 PEZ 16 PEZ 17 PEZ 21 GEN
Mark Dünn, AVP, Registration Development American Kennel Club
Stewart Bauck, General Manager GeneSeek Neogen Corporation
AKC #: DN34605901 DNA Profile #: V784949 Owner(s): Ragterberg Mennes
Mail Order form to
AKC DNA Operations PO Box 900065 Raleigh NC 27675-9065
Number o f DNA certificates _______@ $10 each = $__
Check or money Order □ MasterCard □ Visa □
Account Number:_________________________________
Name on Card:___________________________________
_________ total amountincluded
AmEx □
Exp. Date:__________
ODNA088051 Arco Corporate Drive, Suite 100 Raleigh, NC 27617-3390 Tel 919-816-3600 www.akc.org
Augen / Eyes
★★★
E < * v o >
* *
RAPPORT-OOG-ONDERZOEK★
Certificate★of★eye★examination
European★College★of★Veterinary★Ophthalmologists
Registration★for★The★Netherlands
Raad★van★Beheer★PO★Box★75901★1070★AX★Amsterdam
Tel.:+31.20.6644471★Fax:★+31.20.6710846
ECVO★reg.nr.onderzoek★reg.no.examinatfon
O-NL★no.ECVO★reg.nr.0nderz0ekCTreg.no.★examiner
D ief★ animal
Naamname
Rasbreed
Stamboek★no.registration no.
Microchip★no.microchip no.
Geb.datumdate of birth
-m a a n d — ^ - ja a r -
- month A- y e a r -
Vrouwelijk★femaie Eerder★onderzoek★I I Nee'★ l★ l★ Mannelijk★maie
Eigenaar/houder★ owner/agen t
I★Ja★yes: I★ I★Vrij★ unaffected
l★ l★Voorlopig★niet★vrij★suspicious [
Indien★abnormaal:★ datum,★cert.★no.★-★reg.no.★ onderz........................................
previous examinationOnbeslist★undetermined
Niet★vrij★ atfected
Naamname
Ad★resaddress
date, cert.no.+reg.no. examin.
DNA-Tests Ja★yes Type+datum.Nee★no Vpe + date
Land,★ PCcountry, Zip -country
postcode -Woonpltown l
Ondergetekende gaat akkoord met de regels van het nationale programma ter bestrijding van erfelijke oogafwijkingen en verklaart dat het ter keurina aangeboden dier het hierboven beschreven dier is. Hij/zij gaat akkoord met de onderzoeksvoorwaarden zoals deze zijn vastgelegd in hei Onderzoeksreglement en tevens met openbaarmaking van de gegevens en resultaten van het onderzoek en/of beschikbaarstelling voor door de ECVO goedgekeurd gebruik. Een aantal bepalingen, zoals de voorwaarden waaronder de uitslagen worden doorgegeven aan de rasvereniging is opgenomen op de achterzijde van dit formulier.
The★undersigned★agrees★to★the★rules★of★the★national★scheme★and★confirms★that★the★animal★submitted★for★examination★is★the★one★described★above.★Signature★also★means★that★the★results★are★available★for★official★publication★and★other★ECVO★approved★use.
Handtekening★eigenaar/houder★ signature owner/agent ■
Onderzoek examination7 - dag----------v"
^-dav—-—
Identificatie identification
Datumdate 'ZIa r ----------' Controle★tatoeage★ I★ I★Correct
check tattoo correct-d a y —- — rrronth— yeär
Methode★minimaal:★ Mydriaticum,★ophthalmoscopie★indirect★en★spleetlamp★biomicroscopie★^10x★ Controle★microchip★ l★ .★ l★Correctmethod minimal: Mydriatic, Indirect ophthalmoscopy and binocular biomicroscopy ^dOx check microchip correct
p★ .★ I___ I Onderzocht★vöör★pupilverwijding★ i i Tonometrie★ (zonder mydryaticum)Fxaminarl hafnrp riilatatinn Tonometry (without mydriatic)
Deels★/Niet★leeshaarl★ lAfwijkenril★ l Afwezigpartly /unreadable incorrect absent
Afwijkendl★ I★Afwezigincorrect absent
optional:
l★ l★Onderzocht★vöör★pupilverwijdingExamined before dilatation
l★ l★Ophthalmoscopie,★directDirect Ophthalmoscopy
IG o n io s c o p ie ★ (zonder★mydriaticum)Gonioscopy (without mydriatic)
Anders:Other:
Indien★een★andere★methode★is★toegepast,★ heeft★deze★verklaring★alleen★waarde★indien★vergezeld★van★een★specificerend★certificaat.If another method is used, this form only has value with a specifying certificate.
Commentaar:descriptive comments
Oogziekte★n o .:........................................................★ :★ Jgering★ l★ lmiddelmatig★ I★ I★ernstigeye disease no.: mild moderate severe
Resultaat voor de (als) erfelijk(e) (beschouwde) oogziekten (E-EBOZ): results★for★the★k p -h e d :
VRIJ
1. Membrana Pupillaris Persistens (PPM)★ l ~l
2. Persisterende Hyperpl.Tunica Vasculosa ,Lentis/Primair Vitreum (p h t v l / p h p v ) —
3. Cataract (congenitaal) H D
4. Retina Dysplasie (RD)★ H D
5. Hypoplasie-/Micropapilla l~~i
6. Collie Eye Anomaly (CEA)★ CH]
7. Anders: other:★ .........................................................
8.★L.pectinatum★abn.★ (PLA;★only★after★gonioscopy)★ CH
Interpretatie Interpretation
ONBESLIST NIET
CH I------ liris★ I★ IcorneaI★lens★ l★ llamina
HD ------ Igraad★ 1------ ^ — I★ laraad★2-6
CH H D
□X 1 Z Z ★(multi)focaal
I★ \★ I★ I★geografisch★|★totaal
HD HD
HDX I ★ Ichoroid.★hypoplasie★
l★ \★ I★ Icoloboma★\ | ★ I★anders:
HD HD★ „__ ,
CH--------X I ★ Ifibrae★latae★
—I★ f ★ I★ llaminae\ J ★ locclusio
UNDETERMINED★ AFFECTED
Resultaten geldig voor 12 maanden results★valid★for★ 2 month
11. Entropion/Trichiasis
VRIJ
□ Z I
VOORLOPIG NIET VRIJ
□ Z
NIETVRIJ□ z
12. Ectropion/Macroblepharon C H I C H H D
13. Distichiasis /Ectopische cilie H D H D H D
14. Cornea dystrophie H D C H C H /C I corticaal
15. Cataract (niet-congenitaal)
1 6 . Lensluxatie (primair)
C H
H D
H D ----------
C Hh d v
I post. pol.
I ant.sut. I.
I punctata
I nucleus
17. Retina degeneratie (PRA) C H C H C H___ | anders
18. Anders: other: ......................................UNAFFECTED
I C HSUSP1CICXJS
C CAFFECTED
* ★ “Vrij":★ Het★dier★vertoont★geen★verschijnselen★van★deze,★ erfe lijke★oogziekte(s).★ "N iet★vrij":★ Het★dier★vertoont★de★klin ische★Symptomen★van★de★ (als)★erfelijk(e)★ (beschouwde)★oogziekte★ (E-EBOZ).★"Unaffected"★signifies★that★there★ is★no★clinical★ evidence★o f★the★known★o r★presumed★ hereditary★eye★diseases★ (KP-HED)★specified,★whereas★ "affected"★signifies★that★there★ is★such★evidence.
* * ★ Zeer★geringe★afwijkingen,★ die★mogelijk★passen★ bij★ het★klinische★beeid★van★deze,★als★ E-EBOZ;★ deze★zijn★echter★onvoldoende★specifiek.The★animal★displays★clinical★ features★that★could★ possibly★fit★the★known★or★presumed★ hereditary★eye★diseases★ (KP-HED)★mentioned,★ but★the★changes★are★ inconclusive.
* * * ★ Geringe★afwijkingen★ passend★ in★het★klinisch★ beeid★van★deze,★ als★E-EBOZ.★Voortschrijden★van★ het★proces★moet★dit★bevestigen.★ Herkeuring★o v e r ........ maanden.The★animal★displays★minor,★ but★specific★clinical★signs★of★the★known★or★presumed★hereditary★eye★diseases★ (KP-HED)★mentioned.★ Further★development★will★confirm★the★diagnosis.★ Reexamination★ in ......months.
VOOR★VERDERE★INFORMATIE:★Z.O.Z.★ further★info:★P.T.O. Onderzoeker★ examinerOndergetekende★heeft★bovenstaand★dier★onderzocht★ in★het★ kader★van★ het★ bestrijdingsprogramma★ van★ erfelijke★oogziekten,★met★het★bovengenoemde★resultaat,
T h e undersigned has today examined the above mentioned animal for the hereditary eye disease schem e with the results a s shown.
kleur★/★distributie★ coiour / distributionwit★ RvB★ white national registrygeel★ rasvereniging★ yellow national breed clubroze★ onderzoeker★ Pink examinerwit★ eigenaar/houder★ white owner/agent
Naam
Plaats★ ....................................................................................25-05-’16★© ★e c v o
handtekening★dierenarts,★geautoriseerd★door★de★ECVOsignature examiner, authorized by ECVO -
★★★
E < * v o >
* *
RAPPORT-OOG-ONDERZOEK★
Certificate★of★eye★examination
European★College★of★Veterinary★Ophthalmologists
Registration★for★The★Netherlands
Raad★van★Beheer★PO★Box★75901★1070★AX★Amsterdam
Tel.:+31.20.6644471★Fax:★+31.20.6710846
ECVO★reg.nr.onderzoek★reg.no.examinatfon
O-NL★no.ECVO★reg.nr.0nderz0ekCTreg.no.★examiner
D ief★ animal
Naamname
Rasbreed
Stamboek★no.registration no.
Microchip★no.microchip no.
Geb.datumdate of birth
-m a a n d — ^ - ja a r -
- month A- y e a r -
Vrouwelijk★femaie Eerder★onderzoek★I I Nee'★ l★ l★ Mannelijk★maie
Eigenaar/houder★ owner/agen t
I★Ja★yes: I★ I★Vrij★ unaffected
l★ l★Voorlopig★niet★vrij★suspicious [
Indien★abnormaal:★ datum,★cert.★no.★-★reg.no.★ onderz........................................
previous examinationOnbeslist★undetermined
Niet★vrij★ atfected
Naamname
Ad★resaddress
date, cert.no.+reg.no. examin.
DNA-Tests Ja★yes Type+datum.Nee★no Vpe + date
Land,★ PCcountry, Zip -country
postcode -Woonpltown l
Ondergetekende gaat akkoord met de regels van het nationale programma ter bestrijding van erfelijke oogafwijkingen en verklaart dat het ter keurina aangeboden dier het hierboven beschreven dier is. Hij/zij gaat akkoord met de onderzoeksvoorwaarden zoals deze zijn vastgelegd in hei Onderzoeksreglement en tevens met openbaarmaking van de gegevens en resultaten van het onderzoek en/of beschikbaarstelling voor door de ECVO goedgekeurd gebruik. Een aantal bepalingen, zoals de voorwaarden waaronder de uitslagen worden doorgegeven aan de rasvereniging is opgenomen op de achterzijde van dit formulier.
The★undersigned★agrees★to★the★rules★of★the★national★scheme★and★confirms★that★the★animal★submitted★for★examination★is★the★one★described★above.★Signature★also★means★that★the★results★are★available★for★official★publication★and★other★ECVO★approved★use.
Handtekening★eigenaar/houder★ signature owner/agent ■
Onderzoek examination7 - dag----------v"
^-dav—-—
Identificatie identification
Datumdate 'ZIa r ----------' Controle★tatoeage★ I★ I★Correct
check tattoo correct-d a y —- — rrronth— yeär
Methode★minimaal:★ Mydriaticum,★ophthalmoscopie★indirect★en★spleetlamp★biomicroscopie★^10x★ Controle★microchip★ l★ .★ l★Correctmethod minimal: Mydriatic, Indirect ophthalmoscopy and binocular biomicroscopy ^dOx check microchip correct
p★ .★ I___ I Onderzocht★vöör★pupilverwijding★ i i Tonometrie★ (zonder mydryaticum)Fxaminarl hafnrp riilatatinn Tonometry (without mydriatic)
Deels★/Niet★leeshaarl★ lAfwijkenril★ l Afwezigpartly /unreadable incorrect absent
Afwijkendl★ I★Afwezigincorrect absent
optional:
l★ l★Onderzocht★vöör★pupilverwijdingExamined before dilatation
l★ l★Ophthalmoscopie,★directDirect Ophthalmoscopy
IG o n io s c o p ie ★ (zonder★mydriaticum)Gonioscopy (without mydriatic)
Anders:Other:
Indien★een★andere★methode★is★toegepast,★ heeft★deze★verklaring★alleen★waarde★indien★vergezeld★van★een★specificerend★certificaat.If another method is used, this form only has value with a specifying certificate.
Commentaar:descriptive comments
Oogziekte★n o .:........................................................★ :★ Jgering★ l★ lmiddelmatig★ I★ I★ernstigeye disease no.: mild moderate severe
Resultaat voor de (als) erfelijk(e) (beschouwde) oogziekten (E-EBOZ): results★for★the★k p -h e d :
VRIJ
1. Membrana Pupillaris Persistens (PPM)★ l ~l
2. Persisterende Hyperpl.Tunica Vasculosa ,Lentis/Primair Vitreum (p h t v l / p h p v ) —
3. Cataract (congenitaal) H D
4. Retina Dysplasie (RD)★ H D
5. Hypoplasie-/Micropapilla l~~i
6. Collie Eye Anomaly (CEA)★ CH]
7. Anders: other:★ .........................................................
8.★L.pectinatum★abn.★ (PLA;★only★after★gonioscopy)★ CH
Interpretatie Interpretation
ONBESLIST NIET
CH I------ liris★ I★ IcorneaI★lens★ l★ llamina
HD ------ Igraad★ 1------ ^ — I★ laraad★2-6
CH H D
□X 1 Z Z ★(multi)focaal
I★ \★ I★ I★geografisch★|★totaal
HD HD
HDX I ★ Ichoroid.★hypoplasie★
l★ \★ I★ Icoloboma★\ | ★ I★anders:
HD HD★ „__ ,
CH--------X I ★ Ifibrae★latae★
—I★ f ★ I★ llaminae\ J ★ locclusio
UNDETERMINED★ AFFECTED
Resultaten geldig voor 12 maanden results★valid★for★ 2 month
11. Entropion/Trichiasis
VRIJ
□ Z I
VOORLOPIG NIET VRIJ
□ Z
NIETVRIJ□ z
12. Ectropion/Macroblepharon C H I C H H D
13. Distichiasis /Ectopische cilie H D H D H D
14. Cornea dystrophie H D C H C H /C I corticaal
15. Cataract (niet-congenitaal)
1 6 . Lensluxatie (primair)
C H
H D
H D ----------
C Hh d v
I post. pol.
I ant.sut. I.
I punctata
I nucleus
17. Retina degeneratie (PRA) C H C H C H___ | anders
18. Anders: other: ......................................UNAFFECTED
I C HSUSP1CICXJS
C CAFFECTED
* ★ “Vrij":★ Het★dier★vertoont★geen★verschijnselen★van★deze,★ erfe lijke★oogziekte(s).★ "N iet★vrij":★ Het★dier★vertoont★de★klin ische★Symptomen★van★de★ (als)★erfelijk(e)★ (beschouwde)★oogziekte★ (E-EBOZ).★"Unaffected"★signifies★that★there★ is★no★clinical★ evidence★o f★the★known★o r★presumed★ hereditary★eye★diseases★ (KP-HED)★specified,★whereas★ "affected"★signifies★that★there★ is★such★evidence.
* * ★ Zeer★geringe★afwijkingen,★ die★mogelijk★passen★ bij★ het★klinische★beeid★van★deze,★als★ E-EBOZ;★ deze★zijn★echter★onvoldoende★specifiek.The★animal★displays★clinical★ features★that★could★ possibly★fit★the★known★or★presumed★ hereditary★eye★diseases★ (KP-HED)★mentioned,★ but★the★changes★are★ inconclusive.
* * * ★ Geringe★afwijkingen★ passend★ in★het★klinisch★ beeid★van★deze,★ als★E-EBOZ.★Voortschrijden★van★ het★proces★moet★dit★bevestigen.★ Herkeuring★o v e r ........ maanden.The★animal★displays★minor,★ but★specific★clinical★signs★of★the★known★or★presumed★hereditary★eye★diseases★ (KP-HED)★mentioned.★ Further★development★will★confirm★the★diagnosis.★ Reexamination★ in ......months.
VOOR★VERDERE★INFORMATIE:★Z.O.Z.★ further★info:★P.T.O. Onderzoeker★ examinerOndergetekende★heeft★bovenstaand★dier★onderzocht★ in★het★ kader★van★ het★ bestrijdingsprogramma★ van★ erfelijke★oogziekten,★met★het★bovengenoemde★resultaat,
T h e undersigned has today examined the above mentioned animal for the hereditary eye disease schem e with the results a s shown.
kleur★/★distributie★ coiour / distributionwit★ RvB★ white national registrygeel★ rasvereniging★ yellow national breed clubroze★ onderzoeker★ Pink examinerwit★ eigenaar/houder★ white owner/agent
Naam
Plaats★ ....................................................................................25-05-’16★© ★e c v o
handtekening★dierenarts,★geautoriseerd★door★de★ECVOsignature examiner, authorized by ECVO -
MDR1
VGM O LEK U LA R N A D IAG N O STIKA
tel: +38640566273e-mail: [email protected]
web: www.eurovetgene.com
REFERENCE NO.: 2015-04539 NAME/LABEL:OWNER: JONAHRENATE AGTERBERG-MENNES SPECIES: DOGVLEDDERHUIZEN 3 BREED: AUSTRALIAN SHEPHERDNL-9591 ONSTWEDDE SEX: MALENETHERLANDS MICROCHIP NO.: 981020013491908
TATOO NO.: NOT PROVIDEDPEDIGREE NO.: NOT PROVIDED
GENETIC REPORT
SAMPLE:
SAMPLE TAKEN BY:
REQUESTEDTEST:
B U C C A LSW A B
O W N E R
M U LTI DRUG RESISTANCE (IVERM ECTIN SEN SITIV ITY , M D R1)
RESULT: C LEA R (W T /W T )
COMMENT:
Regarding to the presence of tested mutation animals are classified in three groups:
Affected (mut/m ut) - both alleles carry mutations, disease is clinically manifested Carrier (m ut/wt) - one of tw o alleles carries a mutation, disease is not clinically manifested Clear (w t/wt) - mutation is not present, normal genotype
For each group different breeding strategies should be followed. Breeding of affected and carrier animals should be avoided. If particularly valuable animal is classified as affected it should be bred only w ith clear anim al. In such a case all first Generation siblings will be carriers. If a carrier is bred with clear animal, 50% of siblings are expected to be clear. In case two carriers are bred, 25% of siblings are expected to be clear and 50% are expected to be carriers. However, 25% of siblings are expected to be affected, therefore such breeding practice is discouraged. Genetic test should be done for all animals where genotype cannot be inferred from parent genotypes or if certificate of Genetic Status is required.
For additional information we are available on our phone during working days between 9 a.m. and 3 p.m. or e-mail.
AUTHORIZED SIGN ATU RE: MARIBOR, 22 .05 .2015
Results are valid for laboratory analysed samples only. Accuracy of the data about animal identity is the sole responsibility of the customer/owner. Laboratory is not responsible for false results which arise due to inaccurate animal identity data, false sample labels etc. To the extent the law allows, the maximal compensation for potential false result is limited to the invoiced amount. With the test itis not possibie torule out the presence of other genetic changes which mightaffect the development of the disease. Testing is performed according to the tatest scientific knowledge.
EVG molekularna diagnostika d.o.o. • Grajski trg 1 • SI-2000 Maribor • Slovenia
VGM O LEK U LA R N A D IAG N O STIKA
tel: +38640566273e-mail: [email protected]
web: www.eurovetgene.com
REFERENCE NO.: 2015-04539 NAME/LABEL:OWNER: JONAHRENATE AGTERBERG-MENNES SPECIES: DOGVLEDDERHUIZEN 3 BREED: AUSTRALIAN SHEPHERDNL-9591 ONSTWEDDE SEX: MALENETHERLANDS MICROCHIP NO.: 981020013491908
TATOO NO.: NOT PROVIDEDPEDIGREE NO.: NOT PROVIDED
GENETIC REPORT
SAMPLE:
SAMPLE TAKEN BY:
REQUESTEDTEST:
B U C C A LSW A B
O W N E R
M U LTI DRUG RESISTANCE (IVERM ECTIN SEN SITIV ITY , M D R1)
RESULT: C LEA R (W T /W T )
COMMENT:
Regarding to the presence of tested mutation animals are classified in three groups:
Affected (mut/m ut) - both alleles carry mutations, disease is clinically manifested Carrier (m ut/wt) - one of tw o alleles carries a mutation, disease is not clinically manifested Clear (w t/wt) - mutation is not present, normal genotype
For each group different breeding strategies should be followed. Breeding of affected and carrier animals should be avoided. If particularly valuable animal is classified as affected it should be bred only w ith clear anim al. In such a case all first Generation siblings will be carriers. If a carrier is bred with clear animal, 50% of siblings are expected to be clear. In case two carriers are bred, 25% of siblings are expected to be clear and 50% are expected to be carriers. However, 25% of siblings are expected to be affected, therefore such breeding practice is discouraged. Genetic test should be done for all animals where genotype cannot be inferred from parent genotypes or if certificate of Genetic Status is required.
For additional information we are available on our phone during working days between 9 a.m. and 3 p.m. or e-mail.
AUTHORIZED SIGN ATU RE: MARIBOR, 22 .05 .2015
Results are valid for laboratory analysed samples only. Accuracy of the data about animal identity is the sole responsibility of the customer/owner. Laboratory is not responsible for false results which arise due to inaccurate animal identity data, false sample labels etc. To the extent the law allows, the maximal compensation for potential false result is limited to the invoiced amount. With the test itis not possibie torule out the presence of other genetic changes which mightaffect the development of the disease. Testing is performed according to the tatest scientific knowledge.
EVG molekularna diagnostika d.o.o. • Grajski trg 1 • SI-2000 Maribor • Slovenia
HSF4
Sr&vcsM O LEK U LA R N A D IAG N O STIKA
tel: +38640566273e-mail: [email protected]
web: www.eurovetgene.com
REFERENCE NO.: 2015 - 04539 NAME/LABEL:OWNER: JONAHRENATE AGTERBERG-MENNES SPECIES: DOGVLEDDERHUIZEN 3 BREED: AUSTRALIAN SHEPHERDNL-9591 ONSTWEDDE SEX: MALENETHERLANDS MICROCHIP NO.: 981020013491908
TATOO NO.: NOT PROVIDEDPEDIGREE NO.: NOT PROVIDED
GENETIC REPORT
SAMPLE: B U C C A LS W A B
SAMPLE TAKEN BY: O W N E R
REQUESTED TEST: H ERED ITARY CA TA RA C T(H C )
RESULT: C LEA R (W T /W T )
COMMEIMT:
The test examines presence or absence of HSF4 gene mutation described as the cause of primary hereditary cataract in Australian Shepherds. Regarding to the presence of tested mutation animals are classified in three groups:
Affected (mut/m ut) - both alleles carry m utations, disease is clinically manifestedCarrier (m ut/wt) - one of two alleles carries a mutation, high probability of clinical manifestationClear (w t/w t) - mutation is not present, normal genotype
Hereditary cataract in Australian Shepherds has autosomal dominant mode of inheritance with incomplete penetrance. That means it is not developed in every heterozygous animal carrying deleterious mutation. O ther genetic or environmental factors cannot be excluded in developm ent of the disease. According to the scientific literature the probability of developing the disease is 17 times higher in heterozygous animal comparing to clear anim al. Carriers pass the mutation to their siblings therefore mating of two carrier anim als should be avoided as 25% of puppies will be affected. The test cannot exclude other genetic defects which may be involved in development of hereditary cataract in Australian Shepherds.
For additional information we are available on our phone during working days between 9 a.m . and 3 p.m. or e-mail.
AUTHORIZED SIGN ATURE: M aribor, 22 .05 .2015
lgOj)EKULARN/f DIAGNOSTIKAResult&VB vplifkf.pQa^Mtay^plh'aißbd;sdmples only. Accuracy ofthe data about animal identity is the sole responsibility ofthe customer/owner. Laboratory is not responsibleforfolse results which arise due to inaccurate animal identity data, false sample labels etc. To the extent the law allows, the maximal compensation for potential fatse result is limited to the invoiced amount. With the test it is not possibte to rule out the presence of other genetic changes which might affect the development o f the disease. Testing is performed according to the latest scientific knowledge.
EVG molekularna diagnostika d.o.o. • Grajski trg 1 • SI-2000 Maribor • Slovenia
Sr&vcsM O LEK U LA R N A D IAG N O STIKA
tel: +38640566273e-mail: [email protected]
web: www.eurovetgene.com
REFERENCE NO.: 2015 - 04539 NAME/LABEL:OWNER: JONAHRENATE AGTERBERG-MENNES SPECIES: DOGVLEDDERHUIZEN 3 BREED: AUSTRALIAN SHEPHERDNL-9591 ONSTWEDDE SEX: MALENETHERLANDS MICROCHIP NO.: 981020013491908
TATOO NO.: NOT PROVIDEDPEDIGREE NO.: NOT PROVIDED
GENETIC REPORT
SAMPLE: B U C C A LS W A B
SAMPLE TAKEN BY: O W N E R
REQUESTED TEST: H ERED ITARY CA TA RA CT(H C )
RESULT: C LEA R (W T /W T )
COMMEIMT:
The test examines presence or absence of HSF4 gene mutation described as the cause of primary hereditary cataract in Australian Shepherds. Regarding to the presence of tested mutation animals are classified in three groups:
Affected (mut/m ut) - both alleles carry m utations, disease is clinically manifestedCarrier (m ut/wt) - one of two alleles carries a mutation, high probability of clinical manifestationClear (w t/w t) - mutation is not present, normal genotype
Hereditary cataract in Australian Shepherds has autosomal dominant mode of inheritance with incomplete penetrance. That means it is not developed in every heterozygous animal carrying deleterious mutation. O ther genetic or environmental factors cannot be excluded in developm ent of the disease. According to the scientific literature the probability of developing the disease is 17 times higher in heterozygous animal comparing to clear anim al. Carriers pass the mutation to their siblings therefore mating of two carrier anim als should be avoided as 25% of puppies will be affected. The test cannot exclude other genetic defects which may be involved in development of hereditary cataract in Australian Shepherds.
For additional information we are available on our phone during working days between 9 a.m . and 3 p.m. or e-mail.
AUTHORIZED SIGN ATURE: M aribor, 22 .05 .2015
lgOj)EKULARN/f DIAGNOSTIKAResult&VB vplifkf.pQa^Mtay^plh'aißbd;sdmples only. Accuracy ofthe data about animal identity is the sole responsibility ofthe customer/owner. Laboratory is not responsibleforfolse results which arise due to inaccurate animal identity data, false sample labels etc. To the extent the law allows, the maximal compensation for potential fatse result is limited to the invoiced amount. With the test it is not possibte to rule out the presence of other genetic changes which might affect the development o f the disease. Testing is performed according to the latest scientific knowledge.
EVG molekularna diagnostika d.o.o. • Grajski trg 1 • SI-2000 Maribor • Slovenia
CEA
tel: +38640566273e-mail: [email protected]
web: www.eurovetgene.com
REFERENCE NO.: 2015-04539 NAME/LABEL:OWNER: JONAHRENATE AGTERBERG-MENNES SPECIES: DOGVLEDDERHUIZEN 3 BREED: AUSTRALIAN SHEPHERDNL-9591 ONSTWEDDE SEX: MALENETFIERLANDS MICROCHIP NO.: 981020013491908
TATOO NO.: NOT PROVIDEDPEDIGREE NO.: NOT PROVIDED
GENETIC REPORT
SAMPLE:
SAMPLE TAKEN BY:
REQUESTED TEST:
RESULT:
B U C C A LSW A B
O W N E R
COLLIE EYE A N O M ALY (CEA)
C LEA R (W T /W T )
COMMENT:
Regarding to the presence of tested mutation animals are classified in three groups:
Affected (mut/m ut) - both alleles carry mutations, disease is clinically manifested Carrier (m ut/wt) - one of tw o alleles carries a mutation, disease is not clinically manifested Clear (w t/w t) - mutation is not present, normal genotype
For each group different breeding strategies should be followed. Breeding of affected and carrier animals should be avoided. If particularly valuable animal is classified as affected it should be bred only w ith clear anim al. In such a case all first Generation siblings will be carriers. If a carrier is bred with clear animal, 50% of siblings are expected to be clear. In case two carriers are bred, 25% of siblings are expected to be clear and 50% are expected to be carriers. However, 25% of siblings are expected to be affected, therefore such breeding practice is discouraged. Genetic test should be done for all animals where genotype cannot be inferred from parent genotypes or if certificate of Genetic Status is required.
For additional Information we are available on our phone during working days between 9 a.m. and 3 p.m. or e-mail.
AUTHORIZED SIGN ATURE: MARIBOR, 22.05 .2015
Resu/fPorevote / änalys^cifa'fiiples only. Accuracy ofthe data about animal identity is the sole responsibility ofthe customer/owner. Laboratoryisnot responsible forfalse results which arise due to inaccurate animal identity dataJ false sample labels etc. To the extent the law allows, the maximal compensation for potential false result is limited to the invoiced amount. With the test it is not possible to rule out the presence of other genetic changes which might affect the development ofthe disease. Testing is performed according to the latest scientific knowledge.
EVG molekulama diagnostika d.o.o. • Grajski trg 1 • SI-2000 Maribor • Slovenia
tel: +38640566273e-mail: [email protected]
web: www.eurovetgene.com
REFERENCE NO.: 2015-04539 NAME/LABEL:OWNER: JONAHRENATE AGTERBERG-MENNES SPECIES: DOGVLEDDERHUIZEN 3 BREED: AUSTRALIAN SHEPHERDNL-9591 ONSTWEDDE SEX: MALENETFIERLANDS MICROCHIP NO.: 981020013491908
TATOO NO.: NOT PROVIDEDPEDIGREE NO.: NOT PROVIDED
GENETIC REPORT
SAMPLE:
SAMPLE TAKEN BY:
REQUESTED TEST:
RESULT:
B U C C A LSW A B
O W N E R
COLLIE EYE A N O M ALY (CEA)
C LEA R (W T /W T )
COMMENT:
Regarding to the presence of tested mutation animals are classified in three groups:
Affected (mut/m ut) - both alleles carry mutations, disease is clinically manifested Carrier (m ut/wt) - one of tw o alleles carries a mutation, disease is not clinically manifested Clear (w t/w t) - mutation is not present, normal genotype
For each group different breeding strategies should be followed. Breeding of affected and carrier animals should be avoided. If particularly valuable animal is classified as affected it should be bred only w ith clear anim al. In such a case all first Generation siblings will be carriers. If a carrier is bred with clear animal, 50% of siblings are expected to be clear. In case two carriers are bred, 25% of siblings are expected to be clear and 50% are expected to be carriers. However, 25% of siblings are expected to be affected, therefore such breeding practice is discouraged. Genetic test should be done for all animals where genotype cannot be inferred from parent genotypes or if certificate of Genetic Status is required.
For additional Information we are available on our phone during working days between 9 a.m. and 3 p.m. or e-mail.
AUTHORIZED SIGN ATURE: MARIBOR, 22.05 .2015
Resu/fPorevote / änalys^cifa'fiiples only. Accuracy ofthe data about animal identity is the sole responsibility ofthe customer/owner. Laboratoryisnot responsible forfalse results which arise due to inaccurate animal identity dataJ false sample labels etc. To the extent the law allows, the maximal compensation for potential false result is limited to the invoiced amount. With the test it is not possible to rule out the presence of other genetic changes which might affect the development ofthe disease. Testing is performed according to the latest scientific knowledge.
EVG molekulama diagnostika d.o.o. • Grajski trg 1 • SI-2000 Maribor • Slovenia
PRA
tel: +38640566273e-mail: [email protected]
web: www.eurovetgene.com
REFERENCE NO.: 2015-04539 OWNER:RENATE AGTERBERG-MENNES VLEDDERHUIZEN 3 NL-9591 ONSTWEDDE NETHERLANDS
NAME/LABEL:JONAHSPECIES: DOGBREED: AUSTRALIAN SHEPHERD SEX: MALEMICROCHIP NO.: 981020013491908 TATOO NO.: NOT PROVIDED PEDIGREE NO.: NOT PROVIDED
GENETIC REPORT
SAMPLE: B U C C A LSW A B
SAMPLE TAKEN BY: O W N E R
REQUESTED TEST: PRO G RESSIVE RETIN AL ATRO PH Y (PRA-PRCD)
RESULT: C LEA R (W T /W T )
COMMENT:
Regarding to the presence of tested mutation animals are classified in three groups:
Affected (mut/m ut) - both alleles carry m utations, disease is clinically manifested Carrier (m ut/wt) - one of two alleles carries a mutation, disease is not clinically manifested Clear (w t/wt) - mutation is not present, normal genotype
For each group different breeding strategies should be followed. Breeding of affected and carrier animals should be avoided. If particularly valuable animal is classified as affected it should be bred only with clear anim al. In such a case all first Generation siblings will be carriers. If a carrier is bred with clear animal, 50% of siblings are expected to be clear. In case two carriers are bred, 25% of siblings are expected to be clear and 50% are expected to be carriers. However, 25% of siblings are expected to be affected, therefore such breeding practice is discouraged. Genetic test should be done for all animals where genotype cannot be inferred from parent genotypes or if certificate of Genetic Status is required.
For additional information we are available on our phone during working days between 9 a.m. and 3 p.m. or e-mail.
AUTHORIZED SIGN ATURE: MARIBOR, 22 .05 .2015
ksem ä tMOL£KÜtÄRN>j DIAGNOSTIK*
Resulfsffie fihalys^d stMifdids only. Accuracy of the data about animal identity is the sole responsibility of the customer/owner. Laboratory isnot responsible forfalse results which arise due to inaccurate animal identity data, faise sample labels etc. To the extent the law allows, the maximal compensation for potential false result is limited to the invoiced amount. With the test it is not possible to rule out the presence ofother genetic changes which might affect the development of the disease. Testing is performed according to the latest scientific knowledge.
EVG molekularna diagnostika d.o.o. • Grajski trg 1 • SI-2000 Maribor • Slovenia
DM
tel: +38640566273e-mail: [email protected]
web: www.eurovetgene.com
REFERENCE NO.: 2015-04539 OWNER:RENATE AGTERBERG-MENNES VLEDDERHUIZEN 3 NL-9591 ONSTWEDDE NETHERLANDS
NAME/LABEL:JONAHSPECIES: DOGBREED: AUSTRALIAN SHEPHERD SEX: MALEMICROCHIP NO.: 981020013491908 TATOO NO.: NOT PROVIDED PEDIGREE NO.: NOT PROVIDED
GENETIC REPORT
SAMPLE: B U C C A LSW A B
SAMPLE TAKEN BY: O W N E R
REQUESTED TEST: PRO G RESSIVE RETIN AL ATRO PH Y (PRA-PRCD)
RESULT: C LEA R (W T /W T )
COMMENT:
Regarding to the presence of tested mutation animals are classified in three groups:
Affected (mut/m ut) - both alleles carry m utations, disease is clinically manifested Carrier (m ut/wt) - one of two alleles carries a mutation, disease is not clinically manifested Clear (w t/wt) - mutation is not present, normal genotype
For each group different breeding strategies should be followed. Breeding of affected and carrier animals should be avoided. If particularly valuable animal is classified as affected it should be bred only with clear anim al. In such a case all first Generation siblings will be carriers. If a carrier is bred with clear animal, 50% of siblings are expected to be clear. In case two carriers are bred, 25% of siblings are expected to be clear and 50% are expected to be carriers. However, 25% of siblings are expected to be affected, therefore such breeding practice is discouraged. Genetic test should be done for all animals where genotype cannot be inferred from parent genotypes or if certificate of Genetic Status is required.
For additional information we are available on our phone during working days between 9 a.m. and 3 p.m. or e-mail.
AUTHORIZED SIGN ATURE: MARIBOR, 22 .05 .2015
ksem ä tMOL£KÜtÄRN>j DIAGNOSTIK*
Resulfsffie fihalys^d stMifdids only. Accuracy of the data about animal identity is the sole responsibility of the customer/owner. Laboratory isnot responsible forfalse results which arise due to inaccurate animal identity data, faise sample labels etc. To the extent the law allows, the maximal compensation for potential false result is limited to the invoiced amount. With the test it is not possible to rule out the presence ofother genetic changes which might affect the development of the disease. Testing is performed according to the latest scientific knowledge.
EVG molekularna diagnostika d.o.o. • Grajski trg 1 • SI-2000 Maribor • Slovenia
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Sam
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buc
cal b
rush
Dat
e of b
irth:
23.
02.2
012
Sex:
MId
entit
y of
the a
nim
al h
as n
ot b
een
verif
ied.
30.0
1.20
2005
.02.
2020
10.0
2.20
20
Custo
mer
:Jen
nife
r WA
LTER
Kre
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rgstr
. 44
4780
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refe
ld, D
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iagn
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ké la
bora
tóriu
m, I
lkov
ičov
a 8,
841
04 B
ratis
lava
4, t
el: +
421
905
550
916,
Reg
. No.
(ICO
): 35
7006
29, V
AT:
SK
2020
9061
51,
acco
unts:
SK
5511
0000
0000
2626
2527
86 (T
ATR
SKBX
); CZ
8855
0000
0000
6107
9020
01 (R
ZBCC
ZPP)
; Pay
pal F
S5LN
9AA
C848
S
DN
A A
NA
LYSI
S PR
OTO
COL
FOR
DET
ECTI
ON
OF
HER
EDIT
ARY
DIS
EASE
SPr
otoc
ol N
o. D
2002
0041
90
Bree
d/N
ame
Tatto
o or
RFI
D id
Pedi
gree
num
ber
Labo
rato
ry co
deTy
pe o
f ana
lysis
Res
ult
Aus
tralia
n Sh
ephe
rd /
Ch O
utla
w's
Sure
Hit
9810
2001
3491
908
.20
0205
/U02
14D
M-S
G: S
OD
1ex
on2
- par
tner
lab
N/N
(G/G
)Cl
ear
The r
esul
ts of
anal
ysis
are s
tore
d in
a da
taba
se u
nder
the l
ab co
de 2
0020
5/U
0214
.H
ints:
DM
– D
egen
erat
ive m
yelo
path
y, m
utat
ion
SOD
1:c.1
18G
>A (e
xon
2), a
utos
omal
rece
sive
Perfo
rmed
by
partn
er la
bora
tory
und
er S
lovg
en su
perv
ision
WT/
WT
(G/G
) – C
LEA
R - h
omoz
ygou
s ind
ivid
ual c
arry
ing
two
G al
lele
s – n
on –
affe
cted
(cle
ar)
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/WT
(A/G
) – C
ARR
IER
- het
eroz
ygou
s car
rier c
arry
ing
one a
llele
G an
d on
e AD
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M (A
/A) –
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ECTE
D -
hom
ozyg
ous a
t risk
/affe
cted
indi
vidu
al –
bot
h al
lele
s are
A
Not
ice:
This
prot
ocol
appl
ies e
xclu
sivel
y to
the s
ampl
e and
the d
ata t
hat w
ere s
uppl
ied
by th
e sub
mitt
er. D
NA
anal
ysis
conc
erns
onl
y th
e abo
ve-
men
tione
d di
seas
e. N
o in
form
atio
n re
gard
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the c
usto
mer
as w
ell a
s the
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f the
anal
ysis
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to th
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Dat
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Sonstiges / Miscellaneous
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Cert
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This
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tifie
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at th
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Ow
ner
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Cert
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This
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tifie
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nite
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Deg
ree
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mpi
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IT
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Deg
ree
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May
18,
201
3
Ow
ner
on r
ecor
d: S
HE
RE
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CH
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Witn
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013
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, 201
5.
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AmericAnKennel Club®
RAGTERBERG MENNES = ULEDDERHUIZEN 3 = G5G1 TK ONSTWEDDE S5SS NETHERLANDS
™ Congratulations on your new Australian Shepherd and welcome to the world of purebred dogs. Your AKC registration ^ 5̂ dollars Support numerous AKC efforts to benefit dogs and dog owners. By registering your dog with the AKC, you ■ supported valuable programs such as Canine Search-and-Rescue, the AKC Canine Health Foundation, the AKC Kennel
Inspection Program, public education, canine legislation, and DNA parentage verification.
AKC registration provides wonderful opportunities for every purebred dog lover. The AKC Canine Good Citizen® program is an outstanding way to train your dog in basic obedience, valuable for every family. In addition, many dog owners enjoy the thrill of participating in AKC activities, shows and trials throughout the country. I invite you and your dog to get involved with the AKC!
Please note, if you ordered multiple items at the time of registration, they will be mailed separately and should arrive shortly. These include the AKC Certified Pedigree, the Dog Care and Training Video, Family Dog magazine, and the AKC collar tag. If you did not order a Pedigree, you still have the opportunity to do so. An order form is provided on the back of this letter.
All of us want to be responsible dog owners. To help, the AKC öfters a wealth of information at www.akc.org. Our site lists national and local dog clubs and AKC Canine Good Citizen® evaluators. Please visit us online and on Facebook and Twitter. If we can be of further Service to, please contact us by phone at 919-233-9767 or by email at [email protected].
Sincerely,
8051 Arco Corporate Drive Suite 100Raleigh, NC 27617-3390 www.akc.org
June 18,2015
Dennis B. SprungPresident and Chief Executive Officer
Please separate below and keep for your records.
A M E R I C A N K E N N E L C L U BNAME
OUTLAWS SURE HIT OFA33E OFEL33
BREED
AUSTRALIAN SHEPHERDCOLOR
RED MERLE, WHITE MARKINGS, TAN POINTSSIRE
STORMY LEE'S KING PISTOLDN04437901 04-09 OFA25G OFEL25 AKC DNA#V694331
DAM
OUTLAWS 2HOT4 EWE DN34325501 12-12
BREEDER
SHEREE SANCHEZ
OWNER
RAGTERBERG MENNES ULEDDERHUIZEN 3 G5G1 TK ONSTWEDDE NETHERLANDS
NUMBER
DN34605901SEX
MALEDATE OF BIRTH
FEBRUARY 28, 2012
PROUDLY BRED BY A N AKC BREEDER. OF MERIT
PARTICIPANT....KEMy\iq;
AmericAnKennel Club"
CERTIFICATE ISSUEDJUNE 18,2015
This certificate invalidates all previous certificates issued.
If a date appears after the name and number of the sire and dam, it indicates the issue of the Stud Book Register in which the sire or dam is published.For Transfer Instructions, see back of Certificate.
This Certificate issued with the right to correct or revoke by the American Kennel Club.
R E G I S T R A T I O N C E R T I F I C A T E
AmericAnKennel Club®
RAGTERBERG MENNES = ULEDDERHUIZEN 3 = G5G1 TK ONSTWEDDE S5SS NETHERLANDS
™ Congratulations on your new Australian Shepherd and welcome to the world of purebred dogs. Your AKC registration ^ 5̂ dollars Support numerous AKC efforts to benefit dogs and dog owners. By registering your dog with the AKC, you ■ supported valuable programs such as Canine Search-and-Rescue, the AKC Canine Health Foundation, the AKC Kennel
Inspection Program, public education, canine legislation, and DNA parentage verification.
AKC registration provides wonderful opportunities for every purebred dog lover. The AKC Canine Good Citizen® program is an outstanding way to train your dog in basic obedience, valuable for every family. In addition, many dog owners enjoy the thrill of participating in AKC activities, shows and trials throughout the country. I invite you and your dog to get involved with the AKC!
Please note, if you ordered multiple items at the time of registration, they will be mailed separately and should arrive shortly. These include the AKC Certified Pedigree, the Dog Care and Training Video, Family Dog magazine, and the AKC collar tag. If you did not order a Pedigree, you still have the opportunity to do so. An order form is provided on the back of this letter.
All of us want to be responsible dog owners. To help, the AKC öfters a wealth of information at www.akc.org. Our site lists national and local dog clubs and AKC Canine Good Citizen® evaluators. Please visit us online and on Facebook and Twitter. If we can be of further Service to, please contact us by phone at 919-233-9767 or by email at [email protected].
Sincerely,
8051 Arco Corporate Drive Suite 100Raleigh, NC 27617-3390 www.akc.org
June 18,2015
Dennis B. SprungPresident and Chief Executive Officer
Please separate below and keep for your records.
A M E R I C A N K E N N E L C L U BNAME
OUTLAWS SURE HIT OFA33E OFEL33
BREED
AUSTRALIAN SHEPHERDCOLOR
RED MERLE, WHITE MARKINGS, TAN POINTSSIRE
STORMY LEE'S KING PISTOLDN04437901 04-09 OFA25G OFEL25 AKC DNA#V694331
DAM
OUTLAWS 2HOT4 EWE DN34325501 12-12
BREEDER
SHEREE SANCHEZ
OWNER
RAGTERBERG MENNES ULEDDERHUIZEN 3 G5G1 TK ONSTWEDDE NETHERLANDS
NUMBER
DN34605901SEX
MALEDATE OF BIRTH
FEBRUARY 28, 2012
PROUDLY BRED BY A N AKC BREEDER. OF MERIT
PARTICIPANT....KEMy\iq;
AmericAnKennel Club"
CERTIFICATE ISSUEDJUNE 18,2015
This certificate invalidates all previous certificates issued.
If a date appears after the name and number of the sire and dam, it indicates the issue of the Stud Book Register in which the sire or dam is published.For Transfer Instructions, see back of Certificate.
This Certificate issued with the right to correct or revoke by the American Kennel Club.
R E G I S T R A T I O N C E R T I F I C A T E
Australian Shepherd Association
Officiele rasvereniging Raad van Beheer ( FCI)
This Document declares that the male dog :
Outlaws Sure Hit
NHSB: 3014396
Chip: 981020013491908
Born: 28-02-2012
From the owner R. Agterberg-Mennes is qualified for breeding following allrulesfrom
the Austalian Shepherd Association and the Dutcb kenne! club de Raad yan Beheer member of the FCI.
This document is given by the presidpnfxSt the Australian Shepherd Association.
Mr.M. Agterberg
