EXOTIC LEGENDS JASMINE - NOW LIVING IN A CATTERY IN MONTANA

PICTURE WHEN SHE LOVELY LADY WAS A BABY.

PICTURE FROM SEPTEMBER 2022

Pedigree includes RW SGC, CH, DCG, RW QGC and more.  She is super soft and super friendly. She has oval, almost round large eyes. She has a full and broad muzzle, and prominent whisker pads. She has a FAT tail, but most importantly she is very seet, loving and gentle. A wonderful example of the breed. 

The following are Jasmines results from the testing we have conducted:

Bengal PRA - Clear 

Pyruvate Kinase Deficiency (PK) -  Clear 

Acute Intermittent Porphyria (Variant 1) - Clear  

Acute Intermittent Porphyria (Variant 2) - Clear  

Acute Intermittent Porphyria (Variant 3) - Clear  

Acute Intermittent Porphyria (Variant 4) - Clear  

Acute Intermittent Porphyria (Variant 5) - Clear  

Autoimmune Lymphoproliferative Syndrome - Clear  

Burmese Head Defect (Discovered in Burmese) - Clear  

Chediak-Higashi Syndrome (Discovered in Persian cats) - Clear 

Congenital Adrenal Hyperplasia -Clear  

Congenital Erythropoietic Porphyria -Clear  

Congenital Myasthenic Syndrome (Discovered in Devon Rex and Sphynx) - Clear  

Cystinuria Type 1A - Clear  

Cystinuria Type B (Variant 1) -Clear  

Cystinuria Type B (Variant 2) - Clear  

Cystinuria Type B (Variant 3) - Clear 

Dihydropyrimidinase Deficiency - Clear  

Earfold and Osteochondrodysplasia (Discovered in the Scottish Fold) - Clear  

Factor XII Deficiency (Variant 1) - Clear  

Factor XII Deficiency (Variant 2) - Clear  

Familial Episodic Hypokalaemic Polymyopathy (Discovered in Burmese) - Clear  

GM1 Gangliosidosis - Clear  

GM2 Gangliosidosis - Clear  

GM2 Gangliosidosis, type II (Discovered in Burmese cats) - Clear  

GM2 Gangliosidosis, type II (Discovered in domestic shorthair cats) -Clear  

GM2 Gangliosidosis, type II (Discovered in japanese domestic cats) - Clear  

Glutaric Aciduria Type II - Clear  

Glycogen Storage Disease (Discovered in Norwegian Forest Cat) - Clear 

Hemophilia B (Variant 1) - Clear  

Hemophilia B (Variant 2) - Clear  

Hyperoxaluria type II - Clear  

Hypertrophic Cardiomyopathy (A31P; Discovered in Maine Coon) - Clear  

Hypertrophic Cardiomyopathy (Discovered in Ragdoll) -Clear 

Hypotrichosis (Discovered in Birman cats) - Clear  

Lipoprotein Lipase Deficiency - Clear  

Medication Sensitivity (MDR1) - Clear 

Mucopolysaccharidosis Type I - Clear  

Mucopolysaccharidosis Type VI (mild form) - Clear  

Mucopolysaccharidosis Type VI (severe) -Clear 

Mucopolysaccharidosis Type VII - Clear  

Mucopolysaccharidosis VII - Clear  

Myotonia Congenita - Clear  

Polycystic Kidney Disease (PKD) - Clear 

Progressive Retinal Atrophy (Discovered in Bengal cats) - Clear 

Progressive Retinal Atrophy (Discovered in Persian cats) - Clear 

Progressive Retinal Atrophy (rdAc-PRA) - Clear  

Pyruvate Kinase Deficiency - Clear  

Sphingomyelinosis (Variant 1) - Clear  

Sphingomyelinosis (Variant 2) - Clear  

Spinal Muscular Atrophy (Discovered in Maine Coon) - Clear  

Vitamin D-Dependent Rickets - Clear  

F.I.V. - Negative

FeLV -  Negative

DNA Coat Color - 

1. B/B
2. C/cb - Carrier of Burmese SNOW (Aqua Eyes)
3. A/A
4. N/N
5. D/D
6. E/E

SHE ALSO HAS 2 COPIES OF THE GLITTER GENE