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ON-LINE ORDERS - MOLECULAR GENETICS

Genetic profiling of animals

Step 1

Please select the animal and breed

Step 2Back to animal species selection
Price list

When placing an order, it is necessary to fill in the name of the animal, the sampled material and at least one identification symbol, ie chip number or registration number of the animal.

Animal and sample

Animal speciesBreed
Name of the animal*Date of birth Sex
Chip number*Tattoo number Identification
Material*Date of sample collection
Note for the laboratory

Owner / Breeder (obligatory)

Organization NameReset the owner form
ICTaxState
First nameSurname
StreetNr.Phone
ZIPTownEmail
 
Summary
All prices include VAT
Number of tests selected:
Price for the tests selected:   EUR
Total price:   EUR
Other surcharges
Hard copy of the result, hologram, postal fees (outside of CZE)
Hard copy of the result, hologram, postal fees (CZE)
 

Dog - Australian Shepherd

Genetic ID of the animal
  • Genetic ID of the animal - STR profile (according to ISAG recommendations)
  • STR identification and paternity evaluation
Genetic tests for hereditary diseases
-
  • Alport Syndrome COL4A5 c.513_522delTAATCCAGGA
  • Cobalamin Malabsorption_Imerslund-Gräsbeck syndrome AMN c.3G>A
  • Collie Eye Anomaly NHEJ1 c.588+462_588+8260del7799bp
  • Cone Degeneration CNGB3 complete deletion
  • Cystinuria SLC3A1 c.350delG
  • Degenerative Myelopathy (DM) SOD1 c.118G>A
  • Elliptocytosis SPTB c.6384C>T
  • Hemophilia B - Coagulation Factor IX Deficiency F9 c.1253G>A
  • Hereditary Cataracts HSF4 g.85286582_3insC and g.85286582delC
  • Hyperuricosuria SLC2A9 c.616G>T
  • Leukocyte Adhesion Deficiency ITGB-2 c.107G>C (CLAD)
  • Malignant Hyperthermia RYR-1 c.1640T>C
  • Multi-Drug Resistance ABCB1 c.227_230del
  • Multifocal Retinopathy BEST1 c.73C>T (CMR1)
  • Neuronal Ceroid Lipofuscinosis 6 CLN6 c.829T>C
  • Neuronal Ceroid Lipofuscinosis type 8 CLN8 c.585G>A
  • Oculocutaneous albinism SLC45A2 c.1478G>A
  • Progressive Retinal Atrophy, prcd PRCD c.5G>A
  • Short Tail (Bobtail) T c.189C>G
Genetically determined disease_PTGS2
  • Renal Dysplasia PTGS2 (aka COX-2) promoter length polymorphism
Genetically determined phenotypic variants
    -
  • SuperColorLocus - Locus E (alleles E, Em, Eg, Eh, e, e2, e3); Locus K (alleles K, k); Locus A (alleles Ay, aw, at, a); Locus D (alleles D, d1, d2); Locus S (alleles S, s); locus B (alleles B, bs, bd, bc) + TYRP1 c.555T>G; Harlequin coat color (PSMB
  • Black and Tan coat color (Baset, Welsh Corgi Pembroke), RALY g.1875_1890dupCCCCAGGTCAGAGTTT
  • Black and Tan coat color, Saddle Tan color, allele at ASIP SINE insertion in intron 1
  • Black coat color, allele a ASIP c.288C>T
  • Brown coat color TYRP1 c.555T>G (applicable for Australian Shepherd and Miniature American Shepherd)
  • Curly coat KRT71 c.451C>T
  • Fawn/sable coat color, allele ay ASIP c.246G>T and c.250G>A
  • Furnishings/Wiry pattern RSPO2 167 bp insertion in 3´UTR
  • Hairlessness SGK3 c.283_286delTTAG (applicable for AHT)
  • Harlequin coat color PSMB7 c.146T>G
  • Harlequin coat color PSMB7 c.146T>G
  • LOCUS A, ASIP c.288C>T/ c.246G>T/ c.250G>A/ ASIP SINE_ins
  • LOCUS B, Brown coat color, allele bc_bd_bs |TYRP1 c.121T>A | TYRP1 c.1033_1036del | TYRP1 c.991C>T
  • LOCUS D - allele - d2 Dilution - MLPH c.705G>C
  • LOCUS D - allele d1 - Dilution MLPH c.-22G>A
  • LOCUS E allele e2, Red/ yellow coat color, MC1R c.430G>C (Australian Cattle Dog)
  • LOCUS E, Red/ yellow coat color, MC1R c.916C>T
  • LOCUS K - Black coat color - CBD103 c.67_69delGGG
  • Locus S, Piebald, MITFins_SINE
  • Long hair FGF5 - c.578C>T
  • Long hair FGF5 - c.556_571del16
  • Long hair FGF5 - c.559_560dupGC
  • Long hair/Fluffy hair FGF5 c.284G>T
  • Melanistic mask in fawn or brindle dogs, allele Em, MC1R c.790A>G
   
Genetically determined phenotypic variants_Merle
  • Merle coat pattern SILV SINE insertion (m/Mc/Mc+/Ma/Ma+/M/Mh)
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