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CombiBreed Health Hond UPDATED

CombiBreed Health Hond UPDATED

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 Hyperekplexia (Startle)

GLRA1 36bp del

4 Achromatopsia cd^AMAL

CNGB3 404k kb del

7 Alexander disease

GFAP c.719G>A

8 alpha Fucosidosis

FUCA1 14bp del

12 ARDS

ANLN c.31C>T

13 Ataxia, HACE1

HACE1 c.1001del

14 Bardet-Biedl syndrome 2

BBS2 c.1222G>C

15 Benign juvenile epilepsy

LGI2 c.1552A>T

16 Beta-mannosidosis

MANBA c.560T>A

17 C3 deficiency

C3 c.2136delC

23 Cerebellar ataxia (SDCA1)

KCNJ10 c.986T>C

24 Cerebellar ataxia (SDCA2)

ATP1B2 SINE Ins

25 Cerebellar ataxia GRM1

GRM1 62bp trunc

26 Cerebellar ataxia RAB24

RAB24 c.113A>C

27 Cerebellar ataxia SEL1L

SEL1L c.1972T>C

29 Cerebellar hypoplasia VLDLR

VLDLR c.1713delC

30 Chondrodysplasia

ITGA10 c.2083C>T

31 Intervertebral Disc Disease

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 4

RPGRIP1 44bp ins

38 Cone-rod dystrophy NPHP4

NPHP4 80bp del

42 Copper toxicosis, COMMD1 type

COMMD1 39.7kb del

43 Cornification disorder

NSDHL 14kb del

44 Craniomandibular osteopathy 1

SLC37A2 c.1332C>T

45 Craniomandibular osteopathy 2

SLC37A2 c.1446+1G>A

46 Cyclic neutropenia

AP3B1 1bp ins

47 CYP1A2 deficiency

CYP1A2 c.1117C>T

48 Cystinuria type I - A 1

SLC3A1 c.586C>T

49 Cystinuria type I - A 2

SLC3A1 c.350delG

50 Cystinuria type II - A

SLC3A1 6bp del

51 Cystinuria type II - B

SLC7A9 c.964G>A

52 Deafness MYO7A-related

MYO7A c.3719G>A

53 Deafness, EPS8L2-related

EPS8L2 c.1033_44del

54 Deafness, LOXHD1-related

LOXHD1 c.5747G>C

55 Deafness, PTPRQ-related

PTPRQ c.9230_1insA

58 Dental Hypomineralization

FAM20C c.899C>T

63 Dry Eye Curly Coat Syndrome

FAM83H c.977delC

64 DSRA

MIA3 c.3822+3_+4del

65 Dwarfism, PRKG2-related

PRKG2 c.1634+1G>T

67 Ectodermal dysplasia

PKP1 c.202+1G>C

72 Elliptocytosis

SPTB c.6119C>T

74 Epilepsy, myoclonic

DIRAS1 delAGAC

76 Exercise induced myopathy

ACADVL c.1728C>A

77 Eye malformation

SIXG c.487C>T

79 Familal nephropathy 1

COL4A4 115A>T

80 Familal nephropathy 2

COL4A4 2806C>T

81 Fanconi syndrome

FAN1 317bp del

82 Fecundity

GDF9 c.229C>T

83 Fenobarbital resistentie

ABCB1 c.-6-180T>G

84 Gangliosidosis, GM1 1

GLB1 exon15 delC

85 Gangliosidosis, GM1 2

GLB1 c.179G>A

94 Haemophilia A 1

F8 c.98G>A

95 Haemophilia A 2

F8 c.4824_25ins221

96 Haemophilia A 3

F8 c.1700G>A

97 Haemophilia A 4

F8 c.1469C>G

98 Haemophilia A 5

F8 c.1786C>T

99 Haemophilia B 1

F9 c.731G>A

100 Haemophilia B 2

F9 c.-73del

101 Haemophilia B 4

F9 c.548_553delinsT

102 Haemophilia B 5

F9 c.821_2insA

103 Hepatorenal fibrocystic dis.

INPP5E c.1572+5G>A

109 Hypocatalasia

CAT c.979G>A

110 Hypomyelination

FNIP2 c.880delA

111 Hypophosphatasia

ALPL c.1301T>G

112 Hypothyroidism SLC5A5-related

SLC5A5 c.1172-1G>A

116 Hypotrichosis, recessive 1

SGK3 c.287delTTAG

117 Hypotrichosis, recessive 2

SGK3 c.137_8insT

118 Ichthyosis, ABHD5-related

ABHD5 c.1006_19del

119 Ichthyosis, ASPRV1-related

ASPRV1 c.1052T>C

122 Ichthyosis, SLC27A4-related

SLC27A4 c.1250G>A

125 Imerslund-Grasbeck Syndrome 3

CUBN c.8746+1G>A

126 Inflammatory myopathy

SLC25A12 c.1046T>C

127 Inflammatory pulmonary disease

AKNA c.2717delACAG

128 JEB, LAMA3-related 1

LAMA3 c.8615T>A

129 JEB, LAMB3-related

LAMB3 c.1174T>C

130 JLPP

RAB3GAP1 c.743delC

131-1 Keratinocytic nevi 1

NSDHL c.700G>A

131-2 Keratinocytic nevi 2

NSDHL c.718delGAACA

134 LAD I

ITGB2 c.350T>A

135 LAD III

FERMT3 12bp ins

136 Lagotto storage disease

ATG4D c.1288G>A

137 Laryngeal paralysis

RAPGEF6 c.1793ins36

138 Laryngeal paralysis/pnp

CNTNAP1 c.2810G>A

139 Lens luxation (PLL)

ADAMTS17 G>A

140 Lethal Acrodermatitis

MKLN1 c.400+3A>C

144 Lundehund syndrome

P3H2 c.1849G>C

145 Macrothrombocytopenia 1

TUBB1 c.745 G>A

146 Macrothrombocytopenia 2

TUBB1 c.5G>A

147 Macular Corneal Dystrophy

CHST6 c.814C>A

149 May-Hegglin anomaly

MYH9 c.5521G>A

150 Methaemoglobinaemia 1

CYB5R3 c.580A>C

151 Methaemoglobinaemia 2

CYB5R3 c.214G>A

152 Mucopolysaccharidosis IIIa

SGSH 708-709insC

156 Multidrug resistance 1

ABCB1 4bp del

157 Multifocal retinopathy 1

BEST1 c.73C>T

158 Multifocal retinopathy 2

BEST1 c.482G>A

159 Multifocal retinopathy 3-2

BEST1 c.1466G>T

160 Muscular dystroglycanopathy

LARGE c.1363C>T

161 Muscular dystrophy 1

DMD LINE-1 ins

163 Muscular dystrophy 3

DMD c.531-2A>G

164 Muscular dystrophy 4

DMD c.2668C>T

165 Muscular dystrophy 5

DMD c.2841delT

166 Muscular dystrophy, LAMA2

LAMA2 c.3285G>A

167 Muscular dystrophy, LGMDR3

SGCA c.G224G>A

168-1 Muscular dystrophy, Ullrich 1

COL6A3 c.6210+1G>A

168-2 Muscular dystrophy, Ullrich 2

COL6A3 c.4726C>T

169 Musladin-Lueke syndrome

ADAMTSL2 c.660C>T

170 Myasthenic syndrome, CHAT

CHAT exon6 G>A

171 Myasthenic syndrome, CHRNE 1

CHRNE c.1436_7insG

172 Myasthenic syndrome, CHRNE 2

CHRNE c.633_4insC

173 Myasthenic syndrome, COLQ

COLQ c.1010T>C

174 Myeloencephalopathy, PNPLA8

PNPLA8 c.1169_70dup

176 Centronuclear myopathy

BIN1 IVS10-2A>G

178 Myotonia congenita 2

CLCN1 c.2665insA

179 Myotonia congenita 3

CLCN1 c.2275A>T

180 Myotubular myopathy 1

MTM1 c.465C>A

181 Myotubular myopathy 2

MTM1 c.1151A>C

182 Myotubular myopathy 3

MTM1 c.1467C>T

183 Narcolepsy 1

HCRTR2 exon1 G>A

184 Narcolepsy 2

HCRTR2 SINE ins

185 Narcolepsy 3

HCRTR2 G>A

186 Nasal parakeratosis 2

SUV39H2 delACTT

187 NCL 1 - Teckel

PPT1 c.736-737insC

188 NCL 2

TPP1 c.325delC

189 NCL 4A

ARSG c.296G>A

190 NCL 5

CLN5 c.619C>T

191 NCL 5 GR

CLN5 delAG

192 NCL 6

CLN6 c.829T>C

193 NCL 7

MFSD8 c.846del

194 NCL 8 - 1

CLN8 c.491T>C

195 NCL 8 - 2

CLN8 c.585G>A

196 NCL 8 - Saluki

CLN8 c.349dupT

197 NCL 10

CTSD c.597G>A

198 Neonatal encephalopathy

ATF2 c.152T>G

199 Nephritis, X-linked

COL4A5 C>T

201 Neuroaxonal dystrophy PLA2G6

PLA2G6 c.1579G>A

202 Neuroaxonal dystrophy TECPR2

TECPR2 c.4009C>T

203 Neuroaxonal dystrophy VPS11

VPS11 c.2504A>G

204 Nodular dermatofibrosis

FLCN c.764A>G

205 Obesity predisposition

POMC 14bp del

206 Oculocutaneous albinism OCA2

OCA2 g.31715704A>C

207 Oculocutaneous albinism OCA4 1

SLC45A2 c.1287delC

208 Oculocutaneous albinism OCA4 2

SLC45A2 c.1478G>A

209 Oculoskeletal dysplasia 1

COL9A3 exon1 insG

210 Osteochondrodysplasia

SLC13A1 130kb del

211 Osteochondromatosis

EXT2 c.924C>A

213 Osteogenesis imperfecta 2

SERPINH1 c.977C>T

215 Osteogenesis imperfecta 4

COL1A2 c.936+1G>A

216 P2RY12 bleeding disorder

P2RY12 3bp del

218 Paroxysmal dyskinesia, SOD1

SOD1 c.12delinsCAC

219 Persistent Mullerian Duct

AMHR2 c.262C>T

220 Pituitary dwarfism LHX3

LHX3 7bp del

221 Pituitary dwarfism POU1F1

POU1F1 c.605-3C>A

222 Polycystic kidney disease

PKD1 exon29 G>A

223 Polyneuropathy ARHGEF10

ARHGEF10 10bp del

224 Polyneuropathy GJA9

GJA9 c.1107_8delAG

225 Polyneuropathy NDRG1 1

NDRG1 c.1080-9del10

226 Polyneuropathy NDRG1 2

NDRG1 c.293G>T

227 PRA BBS4-related

BBS4 c.58A>T

228 PRA CCDC66-related

CCDC66 1bp ins

229 PRA CNGA1-related

CNGA1 c.1752_5del

230 PRA IFT122-related

IFT122 c.3176G>A

231 PRA NECAP1-related

NECAP1 c.544G>A

232 PRA PDE6B-related

PDE6B c.2218-23del

233 PRA PRCD-related

PRCD G>A

234 PRA RHO-related

RHO c.11C>G

235 PRA SAG-related

SAG c.1216T>C

236 PRA SLC4A3-related

SLC4A3 insC

237 PRA STK38L-related

STK38L SINE ins

238 PRA TTC8-related

TTC8 c.669delA

239 PRA Type 3 FAM161A-related

FAM161A SINE ins

240 PRA Type B1 HIVEP3-related

HIVEP3 g.1432293G>A

242 Prekallikrein deficiency

KLKB1 exon8 C>T

244 Primary glaucoma ADAMTS10 1

ADAMTS10 exon17 G>A

245 Primary glaucoma ADAMTS10 2

ADAMTS10 c.1441G>A

246 Primary glaucoma ADAMTS17 1

ADAMTS17 delCGTGGT

247 Primary hyperoxaluria

AGXT c.996G>A

253 Pyruvate kinase deficiency 5

PKLR c.1333_8dup

254 Retinal dysplasia

NDP c.653_654insC

256 Rod-cone dysplasia 1a

PDE6B 8bp ins

257 Rod-cone dysplasia 3

PDE6 c.1741delA

258 Rod-cone dysplasia 4

C17H2orf71 insC

259 SCID 1

PRKDC c.10828G>T

260 SCID 2

RAG1 c.2893G>T

261 Scott syndrome

ANO6 g.8912219G>A

262 Sensory Neuropathy 2

FAM134B c.656C>T

263 Shar-Pei Fever

MTBP c.2623G>A

264 Skeletal dysplasia, COL11A2

COL11A2 c.143G>C

265 Spinocerebellar ataxia 1

KCNJ10 c.627C>G

266 Spinocerebellar ataxia 2

SCN81 c.4898G>T

268 Spondylocostal dysostosis

HES7 c.126delG

269 SSADHD

ALDH5A1 c.866G>A

270 Stargardt disease 1

ABCA4 c.4176insC

271 Thrombasthenia 1

ITGA2B exon12 G>C

272 Thrombopathia 1

RASGRP1 delTCT

273 Thrombopathia 2

RASGRP1 insA

274 Thrombopathia 3

RASGRP1 982C>T

276 Urolithiasis (HUU)

SLC2A9 c.616G>T

278 Von Willebrand disease I

VWF c.7437G>A

282 Warburg Micro Syndrome 1

RAB3GAP1 SINE ins

283 X-linked tremor

PLP1 c.110A>C

284 X-SCID

IL2RG 1bp ins

285 Xanthinuria, type I

XDH c.654G>A

286 Xanthinuria, type II 1

MOCOS c.232G>T

287-1 Adult-onset Deafness 1

USP31 g.25681850T>G

287-2 Adult-onset Deafness 2

USP31 g.25714052G>A

287-3 Adult-onset Deafness 3

HS3ST2 g.25819273C>A

287-4 Adult-onset Deafness 4

RBBP6 g.24500625T>G

288-1 Cystinuria Bulldog-type
290 Dilated Cardiomyopathy Risk2

RNF207 c.297-1G>A

291 Ventricular Arrythmias

C20H19orf70 c.325G>A

292 Brachyury

T C189G

293 Improper Coat / Furnishings

RSPO2 167bp indel

295-1 Vachtkleur bruin b^h

TYRP1 c.125G>A

295-2 Vachtkleur bruin b^e

TYRP1 c.1025T>G

295-3 Vachtkleur bruin b^Aussie

TYRP1 c.555T>G

296-1 Vachtkleur extensie e^1

MC1R c.916C>T

296-2 Vachtkleur extensie e^2

MC1R c.432G>C

296-3 Vachtkleur extensie e^3

MC1R c.816_817del

296-4 Vachtkleur extensie E^G

MC1R c.233G>T

296-5 Zwart masker E^M

MC1R c.790A>G

297 Vachtkleur D-locus 1

MLPH c.-22G>A

298 Vachtkleur D-locus 2

MLPH c.705G>C

299 Vachtkleur D-locus 3

MLPH c.667_668insC

306 Vachtkleur Himalayan

TYR c.230G>A

308 Vachtkleur Cocoa

HPS3 c.2420G>A

309 Vachtkleur Roan

USH2A 11kb dup

310-1 Vachtlengte 1

FGF5 c.284G>T

310-2 Vachtlengte 2

FGF5 c.578C>T

310-3 Vachtlengte 3

FGF5 c.556_571del16

310-4 Vachtlengte 4

FGF5 c.559_560dup

310-5 Vachtlengte 5

FGF5 c.368-11T>A

311 Gekrulde vacht 1

KRT71 c.451C>T

312 Gekrulde vacht 2

KRT71 delinsACA


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