Studs - click on the picture to see more photos

Sire - Aluren Tawhiti Nikau [IMP-USA]

Brown [Black] Mackerel

Dam - Southclaw Freida Catlo

Brown [Black] Mackerel

Registered with NZCF & Catzinc

Orivet Genetic Diseases we have tested for.

Frontonasal Dysplasia N/N

Congenital Myasthenic Syndrome N/N

GM2 Gangliosidosis [Korat type] N/N

Niemann-Pick disease - Sphingomyelinosis  N/N

Hereditary Retinal Degeneration PRA  N/N

Myotonia Congenita [Feline] N/N

Spinal Muscular Atrophy N/N

Autoimmune Lymphoproliferative Syndrome N/N

Hyperoxaluria GRHPR  N/N

Mucopolysaccharidosis Type 1. N/N

Chylomicronemia - Lipoprotein Lipase deficiency  N/N

Hypokalaemia Periodic Polymyopathy N/N

Acute Intermitent Porphyria  N/N

Pyruvate Kinase Deficiency [Feline]  N/N

Hypertrophic Cardiomyopathy - ragdoll N/N

Hypertrophic Cardiomyopathy - Maine Coon  N/N

Polycystic Kidney Disease  N/N

Cystinuria SLC3A1  N/N

Mucoploysaccharidosis Type VI  N/N

Haemophilia B  N/N

A/A. B/B. C/C. D/D

Very proud of our home bred boy Te Raa. Looking forward to taking better photos. 3D markings with rich orange glow. A big solid boy with nice muzzle and his eyes are just what we are looking for in our program. I love his full body stripes, down his legs and over his back. Looking forward to seeing this young man mature.

Sire - Pipertwinle Dizney

Brown [Black] Mackerel

Dam - Magadha Lin Tsu Bao Bao [IMP.Taiwan]

Brown [Black] Mackerel

Registered with NZCF & Catzinc

Orivet Genetic Diseases we have tested for.

Frontonasal Dysplasia N/N

Congenital Myasthenic Syndrome N/N

GM2 Gangliosidosis [Korat type] N/N

Niemann-Pick disease - Sphingomyelinosis  N/N

Hereditary Retinal Degeneration PRA  N/N

Myotonia Congenita [Feline] N/N

Spinal Muscular Atrophy N/N

Autoimmune Lymphoproliferative Syndrome N/N

Hyperoxaluria GRHPR  N/N

Mucopolysaccharidosis Type 1. N/N

Chylomicronemia - Lipoprotein Lipase deficiency  N/N

Hypokalaemia Periodic Polymyopathy N/N

Acute Intermitent Porphyria  N/N

Pyruvate Kinase Deficiency [Feline]  N/N

Hypertrophic Cardiomyopathy - ragdoll N/N

Hypertrophic Cardiomyopathy - Maine Coon  N/N

Polycystic Kidney Disease  N/N

Cystinuria SLC3A1  N/N

Mucoploysaccharidosis Type VI  N/N

Haemophilia B  N/N

A/A. B/B. C/C. D/D

Very proud of our home bred boy Te Raa. Looking forward to taking better photos. 3D markings with rich orange glow. A big solid boy with nice muzzle and his eyes are just what we are looking for in our program. I love his full body stripes, down his legs and over his back. Looking forward to seeing this young man mature.

Sire - Alkala Jealousy's a Curse [Import AUS]

Dam - Ambridge Black Berry

Black silver Charcoal

Registered with NZCF  & Catzinc

Brown Charcoal

Orivet Genetic Diseases we have tested for.

Frontonasal Dysplasia N/N

Congenital Myasthenic Syndrome N/N

GM2 Gangliosidosis [Korat type] N/N

Niemann-Pick disease - Sphingomyelinosis  N/N

Hereditary Retinal Degeneration PRA  N/N

Myotonia Congenita [Feline] N/N

Spinal Muscular Atrophy N/N

Autoimmune Lymphoproliferative Syndrome N/N

Hyperoxaluria GRHPR  N/N

Mucopolysaccharidosis Type 1. N/N

Chylomicronemia - Lipoprotein Lipase deficiency  N/N

Hypokalaemia Periodic Polymyopathy N/N

Acute Intermitent Porphyria  N/N

Pyruvate Kinase Deficiency [Feline]  N/N

Hypertrophic Cardiomyopathy - ragdoll N/N

Hypertrophic Cardiomyopathy - Maine Coon  N/N

Polycystic Kidney Disease  N/N

Cystinuria SLC3A1  N/N

Mucoploysaccharidosis Type VI  N/N

Haemophilia B  N/N

Foo is our home bred Charcoal boy. He is very independent and not into cuddles at all but he loves his mates Te Raa and Kapitan. I love the ink in his rosettes and his profile is developing beautifully.

Sire - Pipertwinkle Viscount Five Dagga

Dam - Pipertwinkle Electro Lux

Registered with NZCF  & Catzinc

Brown Charcoal

Orivet Genetic Diseases we have tested for.

Frontonasal Dysplasia N/N

Congenital Myasthenic Syndrome N/N

GM2 Gangliosidosis [Korat type] N/N

Niemann-Pick disease - Sphingomyelinosis  N/N

Hereditary Retinal Degeneration PRA  N/N

Myotonia Congenita [Feline] N/N

Spinal Muscular Atrophy N/N

Autoimmune Lymphoproliferative Syndrome N/N

Hyperoxaluria GRHPR  N/N

Mucopolysaccharidosis Type 1. N/N

Chylomicronemia - Lipoprotein Lipase deficiency  N/N

Hypokalaemia Periodic Polymyopathy N/N

Acute Intermitent Porphyria  N/N

Pyruvate Kinase Deficiency [Feline]  N/N

Hypertrophic Cardiomyopathy - ragdoll N/N

Hypertrophic Cardiomyopathy - Maine Coon  N/N

Polycystic Kidney Disease  N/N

Cystinuria SLC3A1  N/N

Mucoploysaccharidosis Type VI  N/N

Haemophilia B  N/N

Magnum is our home bred brown bengal boy. Super chilled nature. Very chunky with a thick silky coat covered in glitter.

Super proud of this boy.

Sire - Gunner Boston of Heavensgate [IMP.AUST] Blue Silver Mackerel

Dam - Dokota Rose of Heavensgate [IMP.AUST] Blue Tortie Classic

Registered with NZCF & Catzinc

Cream Silver tabby

PKD1 N/N

PK Deficiency N/N

Hereditary Retinal Degeneration PRA     

[No variant detected]

Hypertrophic Cardiomyopathy 

[No variant detected]

Hypertrophic Cardiomyopathy 

[No variant detected]

Hypokalaemia Periodic Polymyopathy 

[No variant detected]

Polycystic Kidney Disease 

[No variant detected]

Hemi has been an absolute treasure to find and I feel very lucky to have him join us. Thank you to our top NZ breeder Gerne. Hemi has Australian imported parents both from Russian lines. I love Hemi's ear tuff & neck ruff and beautiful profile. So excited to see his future here at Pipertwinkle.

Sire - Wariwat Zabar [IMP. Russia]

Black silver Tabby

Dam - ARST Kimber [IMP.Italy]

Black smoke

Registered with NZCF & Catzinc

Black smoke

Orivet Genetic Diseases we have tested for.

Frontonasal Dysplasia N/N

Congenital Myasthenic Syndrome N/N

GM2 Gangliosidosis [Korat type] N/N

Niemann-Pick disease - Sphingomyelinosis  N/N

Hereditary Retinal Degeneration PRA  N/N

Myotonia Congenita [Feline] N/N

Spinal Muscular Atrophy N/N

Autoimmune Lymphoproliferative Syndrome N/N

Hyperoxaluria GRHPR  N/N

Mucopolysaccharidosis Type 1. N/N

Chylomicronemia - Lipoprotein Lipase deficiency  N/N

Hypokalaemia Periodic Polymyopathy N/N

Acute Intermitent Porphyria  N/N

Pyruvate Kinase Deficiency [Feline]  N/N

Hypertrophic Cardiomyopathy - ragdoll N/N

Hypertrophic Cardiomyopathy - Maine Coon  N/N

Polycystic Kidney Disease  N/N

Cystinuria SLC3A1  N/N

Mucoploysaccharidosis Type VI  N/N

Haemophilia B  N/N

Kapitan has a lot of growing to do yet but he's already a totally fluff bomb. He has big feet and long tail, great ear tuffs and nice solid wide muzzle.  We love his gentle social nature. Super excited for his future here at Pipertwinkle.

Sire - Grand Champion Curliwinks Mr Bojangles

Dam - Apokalypt Eclaire

Registered with NZCF & Catzinc

Blue Bi color

Orivet Genetic Diseases we have tested for.

Frontonasal Dysplasia N/N

Congenital Myasthenic Syndrome N/N

GM2 Gangliosidosis [Korat type] N/N

Niemann-Pick disease - Sphingomyelinosis  N/N

Hereditary Retinal Degeneration PRA  N/N

Myotonia Congenita [Feline] N/N

Spinal Muscular Atrophy N/N

Autoimmune Lymphoproliferative Syndrome N/N

Hyperoxaluria GRHPR  N/N

Mucopolysaccharidosis Type 1. N/N

Chylomicronemia - Lipoprotein Lipase deficiency  N/N

Hypokalaemia Periodic Polymyopathy N/N

Acute Intermitent Porphyria  N/N

Pyruvate Kinase Deficiency [Feline]  N/N

Hypertrophic Cardiomyopathy - ragdoll N/N

Hypertrophic Cardiomyopathy - Maine Coon  N/N

Polycystic Kidney Disease  N/N

Cystinuria SLC3A1  N/N

Mucoploysaccharidosis Type VI  N/N

Haemophilia B  N/N

Nick names Rex. We love this boy to bits. Super proud to have a Highglow boy here at Shandalair. Rex is just the bomb and so chilled. He keeps my elder father company and mentors new kittens to the family. He is actually a very solid cat and a total purrer.