GENOPAWS — Pet Genetic Center and Services
Back to packages
For cats

Cat Complete Package

Everything in one — breed + disease + traits, at a bundled price.

Our most complete package for cats — breed identification, disease screening, and trait analysis bundled together at a better price than buying separately.

Price

THB 10,999

Message us on LINE @genopaws for pricing and details — our team is happy to help.

What you get

  • Full breed identification
  • Genetic disease screening
  • Trait analysis
  • Breed Certificate + full health report
  • Bundle price — cheaper than buying separately
  • At-home collection + expert result explanation

How it works

1

Book via LINE OA

Message GENOPAWS on LINE OA @genopaws to consult and choose the DNA package that suits your pet.

2

At-home sample collection

Within Bangkok metro, the GENOPAWS team visits your home to collect the sample — convenient, safe, and stress-free.

3

Expert result explanation

When results return from the lab, our specialist team explains every finding clearly and in detail.

Every package includes at-home sample collection (Bangkok area) and a result explanation by our specialist team.

What we screen for

We screen hundreds of genetic markers and report those relevant to your pet's breed — informational screening, not a diagnosis.

Genetic diseases screened (77)
  • Acute Intermittent Porphyria (Variant 1)
  • Acute Intermittent Porphyria (Variant 2)
  • Acute Intermittent Porphyria (Variant 3)
  • Acute Intermittent Porphyria (Variant 4) (Siamese Type 1)
  • Acute Intermittent Porphyria (Variant 5) (Siamese Type 2)
  • Acute Intermittent Porphyria (Variant 6)
  • Alpha Mannisidosis (Persian/Domestic Type)
  • Autoimmune Lymphoproliferative Syndrome
  • Chylomicronemia - Lipoprotein Lipase Deficiency (Domestic Type)
  • Congenital Adrenal Hyperplasia
  • Congenital Erythropoietic Porphyria, Variant 1 (Feline)
  • Congenital Erythropoietic Porphyria, Variant 2 (Feline)
  • Congenital Hypothyroidism (Feline)
  • Congenital Myasthenic Syndrome
  • Cystinuria, Type 1A (Feline)
  • Cystinuria, Type B, Variant 1 (Feline)
  • Cystinuria, Type B, Variant 2 (Feline)
  • Cystinuria, Type B, Variant 3 (Feline)
  • Cystinuria, Type B, Variant 4 (Feline)
  • Cystinuria, Type B, Variant 5 (Feline)
  • Dihydropyrimidinase Deficiency (Feline)
  • Epidermolysis Bullosa Simplex (Feline)
  • Factor XII Deficiency, Variant 1 (Feline)
  • Factor XII Deficiency, Variant 2 (Feline)
  • Factor XII Deficiency, Variant 3 (Feline)
  • Feline Leukocyte Adhesion Deficiency, Type 1 (Feline)
  • Feline Spongy Encephalopathy (Feline)
  • Folded Ears with Osteochondrodysplasia (Feline)
  • Forebrain Commissural Malformation (Feline)
  • Frontonasal Dysplasia (Burmese Head Defect)
  • Gangliosidosis GM1 (Japanese Domestic Type)
  • Gangliosidosis GM2A (Feline)
  • Glycogen Storage Disease Type IV (Norwegian Forest Cat Type)
  • GM1 - Gangliosidosis
  • GM2 Gangliosidosis (Burmese Type)
  • GM2 Gangliosidosis (Korat Type)
  • GM2 Gangliosidosis, Type II
  • Haemophilia B (Variant 1)
  • Haemophilia B (Variant 2)
  • Hyperoxaluria GRHPR (Domestic Short/Long Hair Type)
  • Hypertrophic Cardiomyopathy - Maine Coon
  • Hypertrophic Cardiomyopathy - Ragdoll
  • Hypertrophic Cardiomyopathy (Sphynx Type Risk Factor) (Feline)
  • Hypogonadotropic Hypogonadism (Feline)
  • Hypokalaemia Periodic Polymyopathy - Burmese
  • Hypotrichosis with Short Life Expectancy (Feline)
  • Inflammatory Linear Verrucous Epidermal Nevus (Feline)
  • L-2-Hydroxyglutaric Aciduria (Feline)
  • Methemoglobinemia, Variant 1 (Feline)
  • Methemoglobinemia, Variant 2 (Feline)
  • Mucolipidosis II (Feline)
  • Mucopolysaccharidosis Type I
  • Mucopolysaccharidosis Type VI (Siamese Type)
  • Mucopolysaccharidosis Type VII, Variant 1 (Feline)
  • Mucopolysaccharidosis Type VII, Variant 2 (Feline)
  • Multiple Drug Resistance (Feline)
  • Myotonia Congenita (Feline)
  • Neuronal Ceroid Lipofuscinosis 6 (Feline)
  • Neuronal Ceroid Lipofuscinosis 7, Variant 1 (Feline)
  • Neuronal Ceroid Lipofuscinosis 7, Variant 2 (Feline)
  • Niemann-Pick C1 Disease, Variant 1 (Feline)
  • Niemann-Pick C1 Disease, Variant 2 (Feline)
  • Niemann-Pick C2 Disease (Feline)
  • Niemann-Pick Disease - Sphingomyelinosis
  • Oculocutaneous Albinism (Feline)
  • Polycystic Kidney Disease
  • Polycystic Kidney Disease (Siberian Type)
  • Primary Congenital Glaucoma (Feline)
  • Progressive Retinal Atrophy (Abyssinian Type)
  • Progressive Retinal Atrophy (Bengal Type)
  • Progressive Retinal Atrophy (Persian Type)
  • Pyruvate Kinase Deficiency (Feline)
  • Rod-Cone Dysplasia (Feline)
  • Spinal Muscular Atrophy
  • Vitamin D-Dependent Rickets Type IB (Feline)
  • Vitamin D-dependent Rickets, Type IA, Variant 1 (Feline)
  • Vitamin D-dependent Rickets, Type IA, Variant 2 (Feline)
Genetic traits analysed (18)
  • Agouti
  • Amber and Russet Coat Colour - E Locus
  • Blood Groups
  • Chocolate & Cinnamon
  • Coat Type - Curly (Devon Rex, Selkirk Rex Type) or Hairless (Sphynx Type) - R Locus
  • Curly Coat - Cornish Rex
  • Dilute (MLPH)
  • Dominant White & White Spotting [W LOCUS]
  • Golden/Sunshine Coat (Siberian Type) - Wb Locus
  • Long Hair / Short Hair
  • Pointed Coat Colour and Albinism - C Locus
  • Polydactyly (Feline)
  • Sex Determination - ZFXY (Feline)
  • Short Tail (Bobtail) - T Locus (Feline)
  • Short Tail (Japanese Bobtail Type) (Feline)
  • Tabby Coat Colour Pattern - Mc Locus (Feline)
  • Ticked - Ti Locus (Feline)
  • White Gloves (Birman Pattern)

Other packages you may like