MyCatDNA™+ DNA Profile with Parentage Service (health test)

Included Health Tests

  • Acute Intermittent Porphyria (Variant 1)
  • Acute Intermittent Porphyria (Variant 2)
  • Acute Intermittent Porphyria (Variant 3)
  • Acute Intermittent Porphyria (Variant 4)
  • Acute Intermittent Porphyria (Variant 5) - NEW!
  • Autoimmune Lymphoproliferative Syndrome
  • Blood Type
  • Burmese Head Defect
  • Chediak-Higashi Syndrome (Discovered in Persian cats) - NEW!
  • Congenital Adrenal Hyperplasia
  • Congenital Erythropoietic Porphyria
  • Congenital Myasthenic Syndrome
  • Cystinuria Type 1A
  • Cystinuria Type B (Variant 1)
  • Cystinuria Type B (Variant 2)
  • Cystinuria Type B (Variant 3)
  • Dihydropyrimidinase Deficiency
  • Earfold and Osteochondrodysplasia (Discovered in the Scottish Fold)
  • Factor XII Deficiency (Variant 1)
  • Factor XII Deficiency (Variant 2) - NEW!
  • Familial Episodic Hypokalaemic Polymyopathy (Discovered in Burmese)
  • Glutaric Aciduria Type II - NEW!
  • Glycogen Storage Disease
  • GM1 Gangliosidosis
  • GM2 Gangliosidosis
  • GM2 Gangliosidosis, type II (Discovered in Burmese cats) - NEW!
  • GM2 Gangliosidosis, type II (Discovered in domestic shorthair cats)
  • GM2 Gangliosidosis, type II (Discovered in japanese domestic cats)
  • Hemophilia B (Variant 1)
  • Hemophilia B (Variant 2)
  • Hyperoxaluria type II
  • Hypertrophic Cardiomyopathy (Discovered in Maine Coon)
  • Hypertrophic Cardiomyopathy (Discovered in Ragdoll)
  • Hypotrichosis (Discovered in Sacred Birman)
  • Lipoprotein Lipase Deficiency
  • Mucopolysaccharidosis Type I
  • Mucopolysaccharidosis Type VI (G1558A variant) - NEW!
  • Mucopolysaccharidosis Type VI (T1427C variant)
  • Mucopolysaccharidosis Type VII
  • Mucopolysaccharidosis VII
  • Multidrug Resistance 1
  • Myotonia Congenita
  • Polycystic Kidney Disease (PKD)
  • Progressive Retinal Atrophy (rdAc-PRA)
  • Progressive Retinal Atrophy (Discovered in Bengal cats)
  • Progressive Retinal Atrophy (Discovered in Persian cats) - NEW!
  • Pyruvate Kinase Deficiency
  • Sphingomyelinosis (Variant 1)
  • Sphingomyelinosis (Variant 2)
  • Spinal Muscular Atrophy
  • Vitamin D-Dependent Rickets

Included Trait Tests

Agouti (A) Locus:

  • Charcoal (Apb)
  • Non-Agouti (a)

Brown (B) Locus:

  • Chocolate (b)
  • Cinnamon (bl)
  • Color (C) Locus:
  • Colorpoint (cb)
  • Colorpoint (cs)
  • Mocha (cm) - NEW!
  • Albinism (c)

Extension (E) Locus:

  • Amber (e)
  • Russet (er)

Dilution (D) Locus:

  • Dilution (d)

White Patterns:

  • Gloves (Birman - White feet)
  • White Spotting/Dominant White

Other Coat Types:

  • Glitter coat - NEW and EXCLUSIVE to Wisdom Health
  • Hairlessness (Discovered in Sphynx)
  • Long hair (mutation M1)
  • Long hair (mutation M2)
  • Long hair (mutation M3)
  • Long hair (mutation M4)
  • Lykoi coat (mutation Ca) - NEW!
  • Lykoi coat (mutation VA) - NEW!
  • Rexing (discovered in Cornish Rex and German Rex)
  • Rexing (discovered in Devon Rex)

Body Features:

  • Short tail (discovered in Japanese Bobtail cats)
  • Short tail (discovered in Manx), two variants
  • Polydactyly (mutation HW)
  • Polydactyly (mutation UK1)
  • Polydactyly (mutation UK2)