DNA Samples
Blood sample in EDTA tubes.
In specific cases, we also send saliva kits to the veterinary centre for sample collection. The kits are very simple to use, and are designed specifically for collecting and preserving DNA samples..
Science
We isolate and process the DNA using the most advanced genomic technology.
Thanks to this, we offer you recommendations that improve the quality of life of your patients.
Support
We send you a report with the results and recommendations for personalising the treatment of each patient.
Additionally, you can always request further support after receiving the results.
GenTest
Genomics analysis for your patients
Genetic screening identifies potential health risks and allows veterinarians and pet owners to improve and extend the quality of life of patients, both preventively and curatively.
Support
If you have any questions, contact our experts at info@omicabiomed.com. We will be delighted to help you.
Time
Time is important for everyone. We deliver results within 15 days from when the samples arrive at our lab
Results
In the GenTest reports, the results are detailed in a user friendly format, easy to interpret for pet owners.
Functionals Gentic Panels
Functional panels, we group breeds phylogenetically, optimising costs to offer you only what you need at a unique price. Exclusively for sale to veterinarians.
CANINE GENTEST 1
General panel with the 10 most common diseases in dogs.
14 common diseases in Breeds Group 1.
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Diseases
General Panel diseases:
- Exercise Induced Collapse (EIC)
- Factor VII Deficiency
- Chondrodysplasia
- Degenerative Myelopathy (DM)
- Hyperuricosuria (SLC)
- Malignant Hyperthermia (MH)
- Primary Lens Luxation (PLL)
- Progressive Retinal Atrophy (prcd-PRA)
- MDR1 – Multi-Drug Resistance
- Von Willebrand Disease Type I (VWD1
Breed group diseases
- Copper Toxicosis
- Type IA Cystinuria
- Hereditary Nasal Parakeratosis (HNPK)
- Narcolepsy
- Degenerative Myelopathy 2 (DM2)
- Stargardt Disease (STGD-PRA)
- Primary Open Angle Glaucoma (POAG)
- Gallbladder Mucocele
- Familial Nephropathy
- Skeletal Dysplasia 2 (SD2)
- Pyruvate Kinase Deficiency (DPK)
- Intestinal Cobalamin Malabsorption (Beagle)
- Mast Cell Tumor Risk
- Osteosarcoma Risk
Breeds
Group 1
- American Cocker Spaniel
- Basset Hound
- Beagle
- Hound
- Petit Basset Griffon Vendéen (PBGV)
- Dachshund (Teckel)
- Dalmatian
- Bernese Mountain Dog
- English Cocker Spaniel
- English Springer Spaniel
- Cavalier King Charles Spaniel
- Irish Water Spaniel
- Brittany Spaniel
- German Shorthaired Pointer
- Great Dane
- Rottweiler
- Flat-coated Retriever
- Golden Retriever
- Labrador Retriever
- Newfoundland
- Borzoi
- Scottish Deerhound
- Irish Wolfhound
- Greyhound
- Sighthound (Lebrel)
- Italian Greyhound
- Ibizan Hound
- Azawakh
Extra diseases
Extra diseases 1, 2, 3
CANINE GENTEST 2
General panel with the 10 most common diseases in dogs.
12 common diseases in Breeds Group 2.
OCULTO (CLICK PARA VER POR QUÉ)
Que este elemento del acordeón esté oculto permite que todos los elementos se vean cerrados. La otra alternativa implicaba incluir código javascript y esta me ha parecido más sencilla.
https://www.markhendriksen.com/how-to-make-the-divi-accordion-closed/
También incluyo la versión de elegant themes que implicaba añadir código.
https://help.elegantthemes.com/en/articles/4748294-make-divi-accordions-closed-by-default
Diseases
General Panel diseases
- Exercise Induced Collapse (EIC)
- Factor VII Deficiency
- Chondrodysplasia
- Degenerative Myelopathy (DM)
- Hyperuricosuria (SLC)
- Malignant Hyperthermia (MH)
- Primary Lens Luxation (PLL)
- Progressive Retinal Atrophy (prcd-PRA)
- MDR1 – Multi-Drug Resistance
- Von Willebrand Disease Type I (VWD1)
Breed group diseases
- Progressive Retinal Atrophy (crd2-PRA)
- Multifocal Retinopathy (CMR1,2,3)
- Achromatopsia (day blindness) (ACHM1)
- Collie Eye Anomaly (CEA)
- Type 3 Cystinuria
- Hemophilia A 1, 2 (Factor VIII)
- Hemophilia B
- Ichthyosis (SLC27A4, ASPRV1)
- Primary Ciliary Dyskinesia
- Intestinal Cobalamin Malabsorption (Collie)
- Congenital Myotonia
- Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND)
Breeds
Breeds of the group 2
- Doberman Pinscher
- Giant Schnauzer
- Standard Schnauzer
- German Shepherd
- Portuguese Water Dog
- Austrian Pinscher
- Beauceron
- Boston Terrier
- Boxer
- French Bulldog
- Miniature Bull Terrier
- Staffordshire Bull Terrier
- Glen of Imaal Terrier
- Bullmastiff
- English Mastiff
- American Pit Bull Terrier
- Belgian Shepherd (Belgian Malinois is one common type)
- Australian Shepherd
- Collie
- Shetland Sheepdog
- Border Collie
- Cardigan Welsh Corgi
- Pembroke Welsh Corgi
- Old English Sheepdog
- Australian Cattle Dog
Extra diseases
| Extra diseases |
1, 2, 3 |
|---|
CANINE GENTEST 3
General panel with the 10 most common diseases in dogs.
11 common disease in the Breed Group 3
OCULTO (CLICK PARA VER POR QUÉ)
Que este elemento del acordeón esté oculto permite que todos los elementos se vean cerrados. La otra alternativa implicaba incluir código javascript y esta me ha parecido más sencilla.
https://www.markhendriksen.com/how-to-make-the-divi-accordion-closed/
También incluyo la versión de elegant themes que implicaba añadir código.
https://help.elegantthemes.com/en/articles/4748294-make-divi-accordions-closed-by-default
Diseases
General panel diseases
- Exercise Induced Collapse (EIC)
- Factor VII Deficiency
- Chondrodysplasia
- Degenerative Myelopathy (DM)
- Hyperuricosuria (SLC)
- Malignant Hyperthermia (MH)
- Primary Lens Luxation (PLL)
- Progressive Retinal Atrophy (prcd-PRA)
- MDR1 – Multi-Drug Resistance
- Von Willebrand Disease Type I (VWD1)
Breed group diseases
- Pyruvate Kinase Deficiency (DPK)
- Craniomandibular Osteopathy (CMO)
- Van den Ende-Gupta Syndrome (VDEGS)
- Congenital Hypothyroidism with Goiter (CHG)
- Spinocerebellar Ataxia (SCA)
- Neuronal Ceroid Lipofuscinosis (NCL4A)
- Polyneuropathy with Ocular Abnormalities (POANV)
- Polycystic Kidney Disease
- Palmoplantar Hyperkeratosis
- X-linked Nephritis
- Myotonia
Breeds
Breeds of the group 3
- Basenji
- Akita
- Chow Chow
- Dingo
- Shar Pei
- Alaskan Malamute
- Siberian Husky
- Afghan Hound
- Saluki
- American Eskimo Dog
- Samoyed
- Pomeranian
- Chihuahua
- Pekingese
- Shih Tzu
- Brussels Griffon
- Pug
- Papillon
- Miniature Pinscher
- Havanese
- Standard Poodle
- Toy Poodle
- Jack Russell Terrier
- Briard
- Australian Terrier
- Yorkshire Terrier
- Cairn Terrier
- West Highland White Terrier
- Scottish Terrier
- Norwich Terrier
Extra diseases
| Extra diseases |
1, 2, 3 |
|---|
OMIBREED
More than 460,000 markers that allow us to personalize genotyping studies, such as breed purity ancestry and other conditions.etc.
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Que este elemento del acordeón esté oculto permite que todos los elementos se vean cerrados. La otra alternativa implicaba incluir código javascript y esta me ha parecido más sencilla.
https://www.markhendriksen.com/how-to-make-the-divi-accordion-closed/
También incluyo la versión de elegant themes que implicaba añadir código.
https://help.elegantthemes.com/en/articles/4748294-make-divi-accordions-closed-by-default
Traits
| Gene Symbol | Gene Name | OMIA Number | Trait |
| TYRP1 | tyrosinase-related protein 1 | 001249 | Coat colour, brown |
| T | T brachyury transcription factor | 000975 | Tail, short |
| ASIP | aspartic peptidase, retroviral-like 1 | 000201 | Coat colour, agouti |
| ASIP | aspartic peptidase, retroviral-like 1 | 000201 | Coat colour, agouti |
| MLPH | melanophilin | 000031 | Alopecia, colour mutant |
| MC1R | melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor) | 001199 | Coat colour, extension |
| MC1R | melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor) | 001199, 001495 | Coat colour, grizzle, Coat colour, extension |
| CBD103 | beta-defensin 103 | 001416 | Coat colour, dominant black |
| PSMB7 | proteasome subunit beta 7 | 001454 | Coat colour, harlequin |
| KRT71 | keratin 71, type II | 000245 | Curly coat |
| MLPH | melanophilin | 000031 | Coat colour, dilute |
| CBD103 | beta-defensin 103 | 001416 | Coat colour, dominant black |
| FGF5 | fibroblast growth factor 5 | 000439 | Hair, long |
| FGF5 | fibroblast growth factor 5 | 000439 | Hair, long |
| FGF5 | fibroblast growth factor 5 | 000439 | Hair, long |
| RSPO2 | R-spondin 2 | 001498 | Improper coat |
| FGF5 | fibroblast growth factor 5 | 000439 | Hair length |
| TYRP1 | tyrosinase-related protein 1 | 001249 | Coat colour, brown |
| TYRP1 | tyrosinase-related protein 1 | 001249 | Coat colour, brown |
| KIT | KIT proto-oncogene receptor tyrosine kinase | 001737 | Coat colour, white spotting, KIT-related |
Diseases
Enfermedades
| Gene Symbol | Gene Name | OMIA Number | Disease |
| CNGB1 | cyclic nucleotide gated channel beta 1 | 000830 | Progressive retinal atrophy |
| ENAM | enamelin | 001805 | Amelogenesis imperfecta |
| SEL1L | sel-1 suppressor of lin-12-like (C. elegans) | 001692 | Ataxia, cerebellar, progressive early-onset |
| LGI2 | leucine-rich repeat LGI family, member 2 | 001596 | Epilepsy, benign familial juvenile |
| C3 | complement component 3 | 000155 | C3 deficiency |
| ARSG | arylsulfatase G | 001503 | Neuronal ceroid lipofuscinosis, 4A |
| ATP1B2 | ATPase, Na+/K+ transporting, beta 2 polypeptide | 002110 | Ataxia, cerebellar, ATP1B2-related |
| CNGB3 | cyclic nucleotide gated channel beta 3 | 001676 | Achromatopsia (cone degeneration, hemeralopia), GSPT |
| VLDLR | very low density lipoprotein receptor | 001947 | Cerebellar hypoplasia, VLDLR-associated |
| MUTYH | mutY DNA glycosylase | 000175 | Cerebellar abiotrophy |
| SDCA1 / ATP1B2 | Ataxia, cerebellar, ATP1B2-related | 002110 | Ataxia, cerebellar, ATP1B2-related |
| SNX14 | sorting nexin 14 | 002034 | Cerebellar cortical degeneration, Hungarian Vizsla |
| TPO | thyroid peroxidase | 000536 | Hypothyroidism |
| ITGA10 | integrin, alpha 10 | 001886 | Chondrodysplasia, disproportionate short-limbed |
| CCDC39 | coiled-coil domain containing 39 | 001540 | Ciliary dyskinesia, primary |
| CLN5 | ceroid-lipofuscinosis, neuronal 5 | 001482 | Neuronal ceroid lipofuscinosis, 5 |
| ITGB2 | integrin subunit beta 2 | 000595 | Leukocyte adhesion deficiency, type I |
| FERMT3 | fermitin family member 3 | 001525 | Leukocyte adhesion deficiency, type III |
| BEST1 | bestrophin 1 | 001444 | Multifocal retinopathy 1 |
| BEST1 | bestrophin 1 | 001553 | Multifocal retinopathy 2 |
| ATP7A | ATPase, Cu++ transporting, alpha polypeptide | 000640 | Menkes disease |
| ATP7B | ATPase, Cu++ transporting, beta polypeptide | 001071 | Wilson disease |
| SLC37A2 | solute carrier family 37 (glucose-6-phosphate transporter), member 2 | 000236 | Craniomandibular osteopathy |
| PDE6B | phosphodiesterase 6B, cGMP-specific, rod, beta | 001674 | Cone-rod dystrophy 1 |
| IQCB1 | IQ motif containing B1 | 001675 | Cone-rod dystrophy 2 |
| RPE65 | retinal pigment epithelium-specific protein 65kDa | 001222 | Leber congenital amaurosis (congenital stationary night blindness) |
| SLC3A1 | solute carrier family 3 (amino acid transporter heavy chain), member 1 | 000256 | Cystinuria, type I – A |
| SLC3A1 | solute carrier family 3 (amino acid transporter heavy chain), member 1 | 001879 | Cystinuria, type II – A |
| SLC3A1 | solute carrier family 3 (amino acid transporter heavy chain), member 1 | 001879 | Cystinuria, type II – A |
| SLC7A9 | solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9 | 001880 | Cystinuria, type II – B |
| FAM20C | family with sequence similarity 20, member C | 002015 | Dental hypomineralization |
| FLCN | folliculin | 001335 | Renal cystadenocarcinoma and nodular dermatofibrosis |
| BEST1 | bestrophin 1 | 001554 | Multifocal retinopathy 3 |
| BEST1 | bestrophin 1 | 001554 | Multifocal retinopathy 3 |
| ADAM9 | ADAM metallopeptidase domain 9 | 001520 | Cone-rod dystrophy 3 |
| SOD1 | superoxide dismutase 1, soluble | 000263 | Degenerative myelopathy |
| GLB1 | galactosidase, beta 1 | 000402 | Gangliosidosis, GM1 (Alaskan Husky) |
| GLB1 | galactosidase, beta 1 | 000402 | Gangliosidosis, GM1 (Gangliosidosis_PWD) |
| GAA | glucosidase, alpha; acid | 000419 | Glycogen storage disease II |
| F9 | coagulation factor IX | 000438 | Haemophilia B |
| SLC27A4 | solute carrier family 27 (fatty acid transporter), member 4 | 001973 | Ichthyosis, SLC27A4-related |
| AMHR2 | anti-Mullerian hormone receptor, type II | 000791 | Persistent Mullerian duct syndrome |
| ATP13A2 | ATPase type 13A2 | 001552 | Neuronal ceroid lipofuscinosis, 12 |
| CLN6 | ceroid-lipofuscinosis, neuronal 6, late infantile, variant | 001443 | Neuronal ceroid lipofuscinosis, 6 |
| PDE6A | phosphodiesterase 6A, cGMP-specific, rod, alpha | 001314 | Rod-cone dysplasia 3 |
| KCNJ10 | potassium channel, inwardly rectifying subfamily J, member 10 : [variant c.627C>G] | 002089 | Ataxia, cerebellar, KCNJ10-related |
| F7 | coagulation factor VII (serum prothrombin conversion accelerator) | 000361 | Factor VII deficiency |
| ABCB4 | ATP-binding cassette, sub-family B (MDR/TAP), member 4 | 001524 | Gallbladder mucoceles |
| GALC | galactosylceramidase | 000578 | Krabbe disease |
| ADAMTS10 | ADAM metallopeptidase with thrombospondin type 1 motif, 10 | 001870 | Glaucoma, primary open angle, ADAMTS10-related |
| G6PC | glucose-6-phosphatase, catalytic subunit | 000418 | Glycogen storage disease Ia |
| GLB1 | galactosidase, beta 1 | 000402 | Gangliosidosis, GM1 |
| HEXB | hexosaminidase B (beta polypeptide) | 001462 | Gangliosidosis, GM2, type II |
| DMD | Duchenne muscular dystrophy | 001081 | Muscular dystrophy, Duchenne type |
| TTC8 | tetratricopeptide repeat domain 8 | 001984 | Golden Retriever PRA 2 |
| AGL | amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase | 001577 | Glycogen storage disease IIIa |
| CNGB1 | cyclic nucleotide gated channel beta 1 | 000830 | Progressive retinal atrophy |
| SLC27A4 | solute carrier family 27 (fatty acid transporter), member 4 | 001973 | Ichthyosis, SLC27A4-related |
| ARHGEF10 | Rho guanine nucleotide exchange factor (GEF) 10 | 001917 | Polyneuropathy, ARHGEF10-related |
| COL1A1 | collagen, type I, alpha 1 | 002126 | Osteogenesis imperfecta, type III, COL1A1-related |
| ASPRV1 | aspartic peptidase, retroviral-like 1 | 002099 | Ichthyosis, ASPRV1-related |
| FOXI3 | forkhead box I3 | 000323 | Ectodermal dysplasia |
| CNGA3 | cyclic nucleotide gated channel alpha 3 | 001481 | Achromatopsia-2 |
| CNGB3 | cyclic nucleotide gated channel beta 3 | 001365 | Achromatopsia (cone degeneration, hemeralopia), AMAL |
| CNGA1 | cyclic nucleotide gated channel alpha 1 | 001977 | Progressive retinal atrophy, CNGA1-related |
| ANO6 | anoctamin 6 | 001353 | Scott Syndrome |
| LHX3 | LIM homeobox 3 | 000307 | Dwarfism, pituitary |
| PKD1 | polycystic kidney disease 1 (autosomal dominant) | 000807 | Polycystic kidney disease |
| SLC2A9 | solute carrier family 2 (facilitated glucose transporter), member 9 | 001033 | Urolithiasis |
| CAT | catalase | 001138 | Hypocatalasia |
| FAM83G | family with sequence similarity 83, member G | 001327 | Hyperkeratosis, palmoplantar |
| KRT10 | keratin 10, type I | 001415 | Hyperkeratosis, epidermolytic |
| FNIP2 | folliculin interacting protein 2 | 000526 | Hypomyelination of the central nervous system |
| CUBN | cubilin (intrinsic factor-cobalamin receptor) | 001786 | Intestinal cobalamin malabsorption, CUBN-related |
| CUBN | cubilin (intrinsic factor-cobalamin receptor) | 001786 | Intestinal cobalamin malabsorption, CUBN-related |
| RAB3GAP1 | RAB3 GTPase activating protein subunit 1 (catalytic) | 001970 | Polyneuropathy, RAB3GAP1-related |
| L2HGDH | L-2-hydroxyglutarate dehydrogenase | 001371 | L-2-hydroxyglutaricacidemia |
| LOC489707 | carbohydrate sulfotransferase 6 | 002071 | Macular corneal dystrophy |
| CLCN1 | chloride channel, voltage-sensitive 1 | 000698 | Myotonia |
| DMD | Duchenne muscular dystrophy | 001081 | Muscular dystrophy, Duchenne type |
| GUSB | glucuronidase, beta | 000667 | Mucopolysaccharidosis VII |
| SGSH | N-sulfoglucosamine sulfohydrolase | 001309 | Mucopolysaccharidosis IIIa |
| GUSB | glucuronidase, beta: “missense mutation (c.866C>T) causing a pathogenic p.P289L change in a conserved functional domain of β-glucuronidase (GUSB)” | 000667 | Mucopolysaccharidosis VII |
| MSTN | myostatin | 000683 | Muscular hypertrophy (double muscling) |
| ADAMTSL2 | ADAMTS-like 2 | 001509 | Musladin-Lueke syndrome |
| CHAT | choline O-acetyltransferase | 002072 | Myasthenic syndrome, congenital |
| CLCN1 | chloride channel, voltage-sensitive 1 | 000698 | Myotonia |
| BIN1 | bridging integrator 1 | 001660 | Myopathy, Great Dane |
| MTM1 | myotubularin 1 | 001508 | Myotubular myopathy 1 |
| HCRTR2 | hypocretin (orexin) receptor 2 | 000703 | Narcolepsy |
| HCRTR2 | hypocretin (orexin) receptor 2 | 000703 | Narcolepsy |
| PPT1 | palmitoyl-protein thioesterase 1 | 001504 | Neuronal ceroid lipofuscinosis, 1 |
| CTSD | cathepsin D | 001505 | Neuronal ceroid lipofuscinosis, 10 |
| CLN8 | ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation) | 001506 | Neuronal ceroid lipofuscinosis, 8 |
| ATF2 | activating transcription factor 2 | 001471 | Neonatal encephalopathy with seizures |
| COL4A5 | collagen, type IV, alpha 5 | 001112 | Nephritis, X-linked |
| MFN2 | mitofusin 2 | 002153 | Neuroaxonal dystrophy |
| COL1A2 | collagen, type I, alpha 2 | 002112 | Osteogenesis Imperfecta |
| SERPINH1 | serpin peptidase inhibitor, clade H (heat shock protein 47), member 1, (collagen binding protein 1) | 001483 | Osteogenesis imperfecta_Dachshund Osteogenesis imperfecta, SERPINH1-related |
| P2RY12 | purinergic receptor P2Y, G-protein coupled, 12 | 001564 | Bleeding disorder due to P2RY12 defect |
| PDP1 | pyruvate dehyrogenase phosphatase catalytic subunit 1 | 001406 | Pyruvate dehydrogenase deficiency |
| PFKM | phosphofructokinase, muscle | 000421 | Glycogen storage disease VII |
| PKLR | pyruvate kinase, liver and RBC | 000844 | Pyruvate kinase deficiency of erythrocyte |
| PKLR | pyruvate kinase, liver and RBC | 000844 | Pyruvate kinase deficiency of erythrocyte |
| PKLR | pyruvate kinase, liver and RBC | 000844 | Pyruvate kinase deficiency of erythrocyte |
| ADAMTS17 | ADAM metallopeptidase with thrombospondin type 1 motif, 17 | 000588 | Lens luxation |
| NDRG1 | N-myc downstream regulated 1 | 002120 | Polyneuropathy |
| ADAMTS17 | ADAM metallopeptidase with thrombospondin type 1 motif, 17 | 001976 | Glaucoma |
| JAK2 | Janus kinase 2 | 000809 | Polycythemia |
| NDRG1 | N-myc downstream regulated 1 | 002120 | Polyneuropathy, NDRG1-related |
| SAG | S-antigen; retina and pineal gland (arrestin) | 001876 | Progressive retinal atrophy, Basenji |
| KLKB1 | kallikrein B, plasma (Fletcher factor) 1 | 000819 | Prekallikrein deficiency |
| PDE6B | phosphodiesterase 6B, cGMP-specific, rod, beta | 001669 | Rod-cone dysplasia 1a |
| PDE6B | phosphodiesterase 6B, cGMP-specific, rod, beta | 000882 | Rod-cone dysplasia 1 |
| COL7A1 | collagen, type VII, alpha 1 | 000341 | Epidermolysis bullosa, dystrophic |
| RAG1 | recombination activating gene 1 | 001574 | Severe combined immunodeficiency disease, autosomal, T cell-negative, B cell-negative, NK cell-positive |
| COL11A2 | collagen, type XI, alpha 2 | 001772 | Skeletal dysplasia 2 (SD2) |
| PRKDC | protein kinase, DNA-activated, catalytic polypeptide | 000220 | Severe combined immunodeficiency disease, autosomal |
| SMOC2 | SPARC related modular calcium binding 2 | 001551 | Brachycephaly |
| CAPN1 | calpain 1, (mu/I) large subunit | 001820 | Ataxia, spinocerebellar, CAPN1-related |
| TGM1 | transglutaminase 1 | 000546 | Ichthyosis, Golden Retriever Ichthyosis, TGM1-related |
| ITGA2B | integrin, alpha 2b (platelet glycoprotein IIb of IIb/IIIa complex, antigen CD41) | 001000 | Thrombasthenia |
| ITGA2B | integrin, alpha 2b (platelet glycoprotein IIb of IIb/IIIa complex, antigen CD41) | 001000 | Thrombasthenia |
| TUBB1 | tubulin, beta 1 class VI | 001001 | Thrombocytopaenia |
| RASGRP1 | RAS guanyl releasing protein 1 (calcium and DAG-regulated) | 001003 | Thrombopathia |
| RASGRP1 | RAS guanyl releasing protein 1 (calcium and DAG-regulated) | 001003 | Thrombopathia |
| VPS13B | Vacuolar protein sorting 13 homolog B (yeast) | 001428 | Trapped Neutrophil Syndrome |
| PLP1 | Proteolipid protein 1 | 000770 | Tremor, X-linked |
| VDR | Vitamin D (1,25- dihydroxyvitamin D3) receptor | 001431 | Vitamin D-deficiency rickets, type II |
| VWF | Von Willebrand factor | 001057 | Von Willebrand disease I |
| VWF | Von Willebrand factor | 001339 | Von Willebrand disease II |
| VWF | Von Willebrand factor | 001058 | Von Willebrand disease III |
| VWF | Von Willebrand factor | 001058 | Von Willebrand disease III |
| IL2RG | Interleukin 2 receptor, gamma | 000899 | Severe combined immunodeficiency disease, X-linked |
Breed
Any
Extra diseases
| Extra diseases | 1, 2, 3 |
|---|
* If you are interested in analyzing any other disease, request that we add it to the panel.
Contact us and we will explain how we can help you
In functional panels, we group breeds phylogenetically, optimizing costs to offer you only what you need at a single price.
Our goal is to offer personalized genomic services adapted to the needs of both veterinarians and breeders as well as the families of furry animals. By optimizing the service, we can offer reduced prices
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Vet
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Vet
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Vet
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