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CombiBreed Health Hond

CombiBreed Health Hond

Deze complete kit biedt een diepgaand onderzoek naar de genetische opmaak van uw hond, waardoor u waardevolle inzichten krijgt in zijn gezondheid en genetische kenmerken.

Bestel het onderzoek

139,95
115,66 (excl. 21% BTW)

Omschrijving

  • Test voor meer dan 255 genetische gezondheidscondities
  • Inzicht in meer dan 35 genetische eigenschappen
  • Inteeltcoëfficiënt
  • Heterozygositeit (genetische diversiteit)

Doeldiersoort en rassen

Hond

Elk ras

Staalname

  • Wisser genetisch
  • EDTA volbloed

Doorlooptijd

30 dagen

Rubriek

Genetische profielen

Code

H3223

Analyses

1 alpha Fucosidosis

FUCA1 14bp del

5 Achromatopsia cd^AMAL

CNGB3 404k kb del

8 Alexander disease

GFAP c.719G>A

9 ARDS

ANLN c.31C>T

11 Amelogenesis imperfecta 3

ACPT c.1189dupG

12 Bardet-Biedl syndrome 2

BBS2 c.1222G>C

13 Benign juvenile epilepsy

LGI2 c.1552A>T

14 Beta-mannosidosis

MANBA c.560T>A

15 C3 deficiency

C3 c.2136delC

22 Cerebellar ataxia 1

GRM1 62bp trunc

23 Cerebellar ataxia 2

RAB24 c.113A>C

25 Cerebellar ataxia (SDCA1)

KCNJ10 c.986T>C

26 Cerebellar ataxia (SDCA2)

ATP1B2 SINE Ins

30 Cerebellar hypoplasia like

VLDLR c.1713delC

31 Chondrodysplasia

ITGA10 c.2083C>T

32 Chondrodystrophy/IVD

FGF4 insMF040221

34 Collie eye anomaly

NHEJ1 7.8kb del

35 Cone-rod dystrophy 1

PDE6B c.2404-6del

36 Cone-rod dystrophy 2

IQCB1 c.952-953insC

37 Cone-rod dystrophy NPHP4

NPHP4 80bp del

38 Copper toxicosis, COMMD1 type

COMMD1 39.7kb del

40 Cone-rod dystrophy 4

RPGRIP1 44bp ins

41 Cornification disorder

NSDHL 14kb del

42 Craniomandibular osteopathy 1

SLC37A2 c.1332C>T

43 Craniomandibular osteopathy 2

SLC37A2 c.1446+1G>A

44 CYP1A2 deficiency

CYP1A2 c.1117C>T

45 Cyclic neutropenia

AP3B1 1bp ins

46 Cystinuria type I - A 1

SLC3A1 c.586C>T

47 Cystinuria type I - A 2

SLC3A1 c.350delG

48 Cystinuria type II - A

SLC3A1 6bp del

49 Cystinuria type II - B

SLC7A9 c.964G>A

50 Deafness, EPS8L2-related

EPS8L2 c.1033_44del

51 Deafness, LOXHD1-related

LOXHD1 c.5747G>C

52 Deafness, PTPRQ-related

PTPRQ c.9230_1insA

55 Dental Hypomineralization

FAM20C c.899C>T

60 Deafness MYO7A-related

MYO7A c.3719G>A

61 Dry Eye Curly Coat Syndrome

FAM83H c.977delC

62 Ectodermal dysplasia

PKP1 c.202+1G>C

67 Elliptocytosis

SPTB c.6119C>T

70 Epilepsy, myoclonic

DIRAS1 delAGAC

71 Eye malformation

SIXG c.487C>T

73 Exercise induced myopathy

ACADVL c.1728C>A

75 Familal nephropathy 1

COL4A4 115A>T

76 Familal nephropathy 2

COL4A4 2806C>T

77 Fanconi syndrome

FAN1 317bp del

78 Fecundity

GDF9 c.229C>T

79 Gangliosidosis, GM1 1

GLB1 exon15 delC

88 Haemophilia A 1

F8 c.98G>A

89 Haemophilia A 2

F8 c.4824_25ins221

90 Haemophilia A 3

F8 c.1700G>A

91 Haemophilia A 5

F8 c.1786C>T

92 Haemophilia B 1

F9 c.731G>A

94 Haemophilia B 2

F9 c.-73del

96 Hepatorenal fibrocystic dis.

INPP5E c.1572+5G>A

97 Nasal parakeratosis 2

SUV39H2 delACTT

101 JEB, LAMA3-related

LAMA3 c.8615T>A

102 JEB, LAMB3-related

LAMB3 c.1174T>C

103 Hypocatalasia

CAT c.979G>A

104 Hypophosphatasia

ALPL c.1301T>G

105 Hypomyelination

FNIP2 c.880delA

108 Hypothyroidism SLC5A5-related

SLC5A5 c.1172-1G>A

109 Ichthyosis, ABHD5-related

ABHD5 c.1006_19del

110 Ichthyosis, ASPRV1-related

ASPRV1 c.1052T>C

113 Ichthyosis, SLC27A4-related

SLC27A4 c.1250G>A

114 Inflammatory myopathy

SLC25A12 c.1046T>C

115 Inflammatory pulmonary disease

AKNA c.2717delACAG

118 Imerslund-Grasbeck Syndrome 3

CUBN c.8746+1G>A

119 JLPP

RAB3GAP1 c.743delC

121 LAD I

ITGB2 c.350T>A

122 LAD III

FERMT3 12bp ins

123 Lagotto storage disease

ATG4D c.1288G>A

124 Laryngeal paralysis

RAPGEF6 c.1793ins36

125 Laryngeal paralysis/pnp

CNTNAP1 c.2810G>A

126 Lens luxation (PLL)

ADAMTS17 G>A

127 Lethal Acrodermatitis

MKLN1 c.400+3A>C

130 Lundehund syndrome

P3H2 c.1849G>C

131 Macular Corneal Dystrophy

CHST6 c.814C>A

133 May-Hegglin anomaly

MYH9 c.5521G>A

134 Methaemoglobinaemia 2

CYB5R3 c.214G>A

135 Mucopolysaccharidosis IIIa

SGSH 708-709insC

136 Mucopolysaccharidosis VI

ARSB c.910G>A

139 Multidrug resistance 1

ABCB1 4bp del

140 Fenobarbital resistentie

ABCB1 c.-6-180T>G

141 Multifocal retinopathy 1

BEST1 c.73C>T

142 Multifocal retinopathy 2

BEST1 c.482G>A

143 Multifocal retinopathy 3-1

BEST1 c1388del

144 Multifocal retinopathy 3-2

BEST1 c.1466G>T

149 Muscular dystrophy, LAMA2

LAMA2 c.3285G>A

150 Muscular dystrophy, LGMDR3

SGCA c.G224G>A

151-1 Muscular dystrophy, Ullrich 1

COL6A3 c.6210+1G>A

151-2 Muscular dystrophy, Ullrich 2

COL6A3 c.4726C>T

152 Muscular dystroglycanopathy

LARGE c.1363C>T

153 Musladin-Lueke syndrome

ADAMTSL2 c.660C>T

154 Myasthenic syndrome, CHAT

CHAT exon6 G>A

155 Myeloencephalopathy, PNPLA8

PNPLA8 c.1169_70dup

156 Myasthenic syndrome, CHRNE 1

CHRNE c.1436_7insG

157 Myasthenic syndrome, CHRNE 2

CHRNE c.633_4insC

158 Myasthenic syndrome, COLQ

COLQ c.1010T>C

159 Myopathy

BIN1 IVS10-2A>G

161 Myotonia congenita 2

CLCN1 c.2665insA

162 Myotonia congenita 3

CLCN1 c.2275A>T

163 Myotubular myopathy 1

MTM1 c.465C>A

164 Myotubular myopathy 2

MTM1 c.1151A>C

165 Myotubular myopathy 3

MTM1 c.1467C>T

166 Narcolepsy 1

HCRTR2 exon1 G>A

167 Narcolepsy 2

HCRTR2 SINE ins

168 Narcolepsy 3

HCRTR2 G>A

169 NCL1 - Teckel

PPT1 c.736-737insC

170 NCL2

TPP1 c.325delC

172 NCL5

CLN5 c.619C>T

173 NCL6

CLN6 c.829T>C

174 NCL5 GR

CLN5 delAG

175 NCL8 - 1

CLN8 c.491T>C

176 NCL8 - 2

CLN8 c.585G>A

177 NCL8 - Saluki

CLN8 c.349dupT

178 NCL10

CTSD c.597G>A

179 Neonatal encephalopathy

ATF2 c.152T>G

180 Nephritis, X-linked

COL4A5 C>T

182 Neuroaxonal dystrophy TECPR2

TECPR2 c.4009C>T

183 Neuroaxonal dystrophy PLA2G6

PLA2G6 c.1579G>A

184 Neuroaxonal dystrophy VPS11

VPS11 c.2504A>G

185 Nodular dermatofibrosis

FLCN c.764A>G

186 Obesity predisposition

POMC 14bp del

187 Oculocutaneous albinism OCA2

OCA2 g.31715704A>C

188 Oculocutaneous albinism OCA4 1

SLC45A2 c.1287delC

189 Oculocutaneous albinism OCA4 2

SLC45A2 c.1478G>A

190 Oculoskeletal dysplasia 1

COL9A3 exon1 insG

192 Osteogenesis imperfecta 2

SERPINH1 c.977C>T

194 Osteochondrodysplasia

SLC13A1 130kb del

195 P2RY12 bleeding disorder

P2RY12 3bp del

197 Paroxysmal dyskinesia, SOD1

SOD1 c.12delinsCAC

198 Persistent Mullerian Duct

AMHR2 c.262C>T

199 Pituitary dwarfism LHX3

LHX3 7bp del

200 Dwarfism, PRKG2-related

PRKG2 c.1634+1G>T

201 Pituitary dwarfism POU1F1

POU1F1 c.605-3C>A

202 Polycystic kidney disease

PKD1 exon29 G>A

203 Polyneuropathy ARHGEF10

ARHGEF10 10bp del

204 Polyneuropathy GJA9

GJA9 c.1107_8delAG

205 Polyneuropathy NDRG1 1

NDRG1 c.1080-9del10

206 Polyneuropathy NDRG1 2

NDRG1 c.293G>T

207 Shar-Pei Fever

MTBP c.2623G>A

208 PRA BBS4-related

BBS4 c.58A>T

209 PRA CCDC66-related

CCDC66 1bp ins

210 PRA CNGA1-related

CNGA1 c.1752_5del

211 PRA CNGB1-related

CNGB1 indel

212 PRA IFT122-related

IFT122 c.3176G>A

213 PRA NECAP1-related

NECAP1 c.544G>A

214 PRA PRCD-related

PRCD G>A

215 PRA PDE6B-related

PDE6B c.2218-23del

216 PRA RHO-related

RHO c.11C>G

217 PRA SAG-related

SAG c.1216T>C

218 PRA SLC4A3-related

SLC4A3 insC

219 PRA STK38L-related

STK38L SINE ins

220 PRA TTC8-related

TTC8 c.669delA

221 PRA Type 3 FAM161A-related

FAM161A SINE ins

222 PRA Type B1 HIVEP3-related

HIVEP3 g.1432293G>A

224 Prekallikrein deficiency

KLKB1 exon8 C>T

226 Primary glaucoma ADAMTS10 1

ADAMTS10 exon17 G>A

227 Primary glaucoma ADAMTS10 2

ADAMTS10 c.1441G>A

228 Primary glaucoma ADAMTS17 1

ADAMTS17 delCGTGGT

229 Primary hyperoxaluria

AGXT c.996G>A

233 Retinal dysplasia

NDP c.653_654insC

236 Rod-cone dysplasia 1a

PDE6B 8bp ins

237 Rod-cone dysplasia 3

PDE6 c.1741delA

238 Rod-cone dysplasia 4

C17H2orf71 insC

239 SCID 1

PRKDC c.10828G>T

240 SCID 2

RAG1 c.2893G>T

241 Sensory Neuropathy 2

FAM134B c.656C>T

242 Skeletal dysplasia 2

COL11A2 c.143G>C

243 Scott syndrome

ANO6 g.8912219G>A

244 Spinocerebellaire ataxie

KCNJ10 c.627C>G

245 Spinocerebellaire ataxie 2

SCN81 c.4898G>T

247 Spondylocostal dysostosis

HES7 c.126delG

248 Stargardt disease 1

ABCA4 c.4176insC

249 SSADHD

ALDH5A1 c.866G>A

250 Thrombasthenia 1

ITGA2B exon12 G>C

251 Macrothrombocytopenia 1

TUBB1 c.745 G>A

252 Macrothrombocytopenia 2

TUBB1 c.5G>A

253 Thrombopathia 1

RASGRP1 delTCT

254 Thrombopathia 2

RASGRP1 insA

255 Thrombopathia 3

RASGRP1 982C>T

257 Urolithiasis (HUU)

SLC2A9 c.616G>T

259 Von Willebrand disease I

VWF c.7437G>A

263 Warburg Micro Syndrome 1

RAB3GAP1 SINE ins

264 Xanthinuria, type I

XDH c.654G>A

265 Xanthinuria, type II 1

MOCOS c.232G>T

266 X-linked tremor

PLP1 c.110A>C

267 X-SCID

IL2RG 1bp ins

268-1 Adult-onset Deafness 1

USP31 g.25681850T>G

268-2 Adult-onset Deafness 2

USP31 g.25714052G>A

268-3 Adult-onset Deafness 3

HS3ST2 g.25819273C>A

268-4 Adult-onset Deafness 4

RBBP6 g.24500625T>G

270 Ventricular Arrythmias

C20H19orf70 c.325G>A

270-1 Cystinuria Bulldog-type
271 Brachyury

T C189G

272 Improper Coat / Furnishings

RSPO2 167bp indel

274-1 Vachtkleur bruin b^h

TYRP1 c.125G>A

274-2 Vachtkleur bruin b^e

TYRP1 c.1025T>G

274-3 Vachtkleur bruin b^Aussie

TYRP1 c.555T>G

275-1 Vachtkleur extensie e^1

MC1R c.916C>T

275-2 Vachtkleur extensie e^2

MC1R c.432G>C

275-3 Vachtkleur extensie e^3

MC1R c.816_817del

275-4 Vachtkleur extensie E^G

MC1R c.233G>T

275-5 Zwart masker E^M

MC1R c.790A>G

276 Vachtkleur D-locus 1

MLPH c.-22G>A

277 Vachtkleur D-locus 2

MLPH c.705G>C

278 Vachtkleur D-locus 3

MLPH c.667_668insC

284 Vachtkleur Himalayan

TYR c.230G>A

286 Vachtkleur Cocoa

HPS3 c.2420G>A

287 Vachtkleur Roan

USH2A 11kb dup

288-1 Vachtlengte 1

FGF5 c.284G>T

288-2 Vachtlengte 2

FGF5 c.578C>T

288-3 Vachtlengte 3

FGF5 c.556_571del16

288-4 Vachtlengte 4

FGF5 c.559_560dup

288-5 Vachtlengte 5

FGF5 c.368-11T>A

290 Curly coat 1

KRT71 c.451C>T

291 Curly coat 2

KRT71 delinsACA


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