Our Kings
猫爸爸们

HANDSOME DADDIES
英气十足ฅ(๑ ̀ㅅ ́๑)ฅ

 
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Fontenoy Bruno of CreamTofu

AKA BVLGARI, GARI

British Longhair

Champion bloodline

Black Golden Shell/Chinchilla ny 12
D.O.B. Jan 02 2020

Optimal Selection genetic test done.

Blood Type: Ab

Chocolate Carrier

No genetic health predispositions.

FIV test: negative

Felv test: negative

Current stud

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OnceUponA Valentino of CreamTofu

​​AKA TINO

Persian

Lilac Bi Color
D.O.B. Jul 27 2020

Optimal Selection genetic test done.

Blood Type: AA

No genetic health predispositions.

FIV test: negative

Felv test: negative

Future stud

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Copper of BunnyBossPetSales

AKA COPPER

British Shorthair

Black Golden Shaded ny 11

Optimal Selection genetic test done

Blood Type: AA

Dilution Carrier

Long coat Carrier

No genetic health predispositions.

FIV test: negative

Felv test: negative

Stud on loan (no longer being used)
 

Copper is a sweet ny 11 british shorthair owned by BunnyBossPetSales, was generously loaned to us to begin our breeding program with our girl Longan, while Gari matured. He is a complete gentleman and loves to greet & cuddle with anyone.

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CH 23rd AVENUE Time Will Tell of OnceUponA

AKA TIMMY

Persian

Lilac White

Optimal Selection genetic test done

Blood Type: AA

No genetic health predispositions.

FIV test: negative

Felv test: negative
 

Stud on loan (no longer being used)
 

Timmy is absolutely affectionate and nice, he sweetly took La Mer when we sent her to him since our Tino is not yet matured. He is a great stud owned by Janet who runs OnceUponA Cattery that delicately breeds persian kittens.
 

Optimal Selection Included Health Tests

(Copied and pasted directly from Optimal Selection™ Feline)

  • 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

  • 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