Our Queens
F1 Drinkwater Bala of KingSavannahs
Bala is our biggest Queen weighing in at over 30 pounds. She is independent and confident and a terrific mother. Her cool tone coloring and black nose give her and her babies a stunning look.Â
Bala's disease testing resultsÂ
Diseases
Disease Name
Genotype
Interpretation
Acute Intermittent Porphyria, Variant 1
WT/WT
Normal (clear)
Acute Intermittent Porphyria, Variant 2
WT/WT
Normal (clear)
Acute Intermittent Porphyria, Variant 3
WT/WT
Normal (clear)
Acute Intermittent Porphyria, Variant 4 (Siamese Type 1)
WT/WT
Normal (clear)
Acute Intermittent Porphyria, Variant 5 (Siamese Type 2)
WT/WT
Normal (clear)
Acute Intermittent Porphyria, Variant 6
WT/WT
Normal (clear)
Autoimmune Lymphoproliferative Syndrome
WT/WT
Normal (clear)
WT/WT
Normal (clear)
Congenital Adrenal Hyperplasia
WT/WT
Normal (clear)
Congenital Erythropoietic Porphyria, Variant 1
WT/WT
Normal (clear)
Congenital Erythropoietic Porphyria, Variant 2
WT/WT
Normal (clear)
WT/WT
Normal (clear)
Congenital Myasthenic Syndrome
WT/WT
Normal (clear)
WT/WT
Normal (clear)
No Result
No Result
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
Dihydropyrimidinase Deficiency
WT/WT
Normal (clear)
Factor XII Deficiency, Variant 1
WT/WT
Normal (clear)
Feline Leukocyte Adhesion Deficiency, Type 1
WT/WT
Normal (clear)
WT/WT
Normal (clear)
Glycogen Storage Disease, Type IV
WT/WT
Normal (clear)
WT/WT
Normal (clear)
GM2 Gangliosidosis, Type II (Burmese Type)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
GM2 Gangliosidosis, Type II (Japanese Domestic Type)
WT/WT
Normal (clear)
GM2 Gangliosidosis, Type II (Korat Type)
WT/WT
Normal (clear)
WT/WT
X-Linked Female Normal
WT/WT
X-Linked Female Normal
WT/WT
Normal (clear)
Hypertrophic Cardiomyopathy (Maine Coon Type)
WT/WT
Normal (clear)
Hypertrophic Cardiomyopathy (Ragdoll Type)
WT/WT
Normal (clear)
Hypokalemic Periodic Paralysis
WT/WT
Normal (clear)
Hypotrichosis with Short Life Expectancy
WT/WT
Normal (clear)
WT/WT
Normal (clear)
Mucopolysaccharidosis Type VI (Modifier)
WT/WT
Normal (clear)
Mucopolysaccharidosis Type VI (Siamese Type)
WT/WT
Normal (clear)
Mucopolysaccharidosis Type VII, Variant 1
WT/WT
Normal (clear)
Mucopolysaccharidosis Type VII, Variant 2
WT/WT
Normal (clear)
WT/WT
Normal (clear)
No Result
No Result
Niemann-Pick C1 Disease, Variant 1
WT/WT
Normal (clear)
Niemann-Pick C1 Disease, Variant 2
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
Progressive Retinal Atrophy (Abyssinian Type)
WT/WT
Normal (clear)
Progressive Retinal Atrophy (Persian Type)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
Vitamin D-dependent Rickets, Type IA, Variant 1
WT/WT
Normal (clear)
Vitamin D-dependent Rickets, Type IA, Variant 2
WT/WT
Normal (clear)
F1 IWannaSavannah Ayla Armani of KingSavannahs
Ayla is a favorite and deserves the attention. We love everything about her; structure, coat, personality and size... Ayla is impressive and THOSE EARS!
Ayla's disease testing resultsÂ
Disease Name
Genotype
Interpretation
Acute Intermittent Porphyria, Variant 1
WT/WT
Normal (Clear)
Acute Intermittent Porphyria, Variant 3
WT/WT
Normal (Clear)
Acute Intermittent Porphyria, Variant 4 (Siamese Type 1)
WT/WT
Normal (Clear)
Acute Intermittent Porphyria, Variant 5 (Siamese Type 2)
WT/WT
Normal (Clear)
Acute Intermittent Porphyria, Variant 6
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Autoimmune Lymphoproliferative Syndrome
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Congenital Adrenal Hyperplasia
WT/WT
Normal (Clear)
Congenital Erythropoietic Porphyria, Variant 1
WT/WT
Normal (Clear)
Congenital Erythropoietic Porphyria, Variant 2
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Congenital Myasthenic Syndrome
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Dihydropyrimidinase Deficiency
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Factor XII Deficiency, Variant 1
WT/WT
Normal (Clear)
Factor XII Deficiency, Variant 2
WT/WT
Normal (Clear)
Factor XII Deficiency, Variant 3
WT/WT
Normal (Clear)
Feline Immunodeficiency Virus (FIV) Infection Risk Modifier
WT/WT
No Increased Resistance to FIV Infection
Feline Leukocyte Adhesion Deficiency, Type 1
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Forebrain Commissural Malformation
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Glycogen Storage Disease, Type IV
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
GM2 Gangliosidosis, Type II (Burmese Type)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
GM2 Gangliosidosis, Type II (Japanese Domestic Type)
WT/WT
Normal (Clear)
GM2 Gangliosidosis, Type II (Korat Type)
WT/WT
Normal (Clear)
WT/WT
X-Linked Female Normal
WT/WT
X-Linked Female Normal
WT/WT
Normal (Clear)
Hypertrophic Cardiomyopathy (Maine Coon Type)
WT/WT
Normal (Clear)
Hypertrophic Cardiomyopathy (Ragdoll Type)
WT/WT
Normal (Clear)
Hypertrophic Cardiomyopathy (Sphynx Type Risk Factor)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Hypokalemic Periodic Paralysis
WT/WT
Normal (Clear)
Hypotrichosis with Short Life Expectancy
WT/WT
Normal (Clear)
Inflammatory Linear Verrucous Epidermal Nevus
WT/WT
X-Linked Female Normal
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Mucopolysaccharidosis Type VI (Modifier)
WT/WT
Normal (Clear)
Mucopolysaccharidosis Type VI (Siamese Type)
WT/WT
Normal (Clear)
Mucopolysaccharidosis Type VII, Variant 1
WT/WT
Normal (Clear)
Mucopolysaccharidosis Type VII, Variant 2
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
No Result
No Result
Neuronal Ceroid Lipofuscinosis 6
WT/WT
Normal (Clear)
Neuronal Ceroid Lipofuscinosis 7, Variant 1
WT/WT
Normal (Clear)
Neuronal Ceroid Lipofuscinosis 7, Variant 2
WT/WT
Normal (Clear)
Niemann-Pick C1 Disease, Variant 1
No Result
No Result
Niemann-Pick C1 Disease, Variant 2
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Polycystic Kidney Disease (Siberian Type)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Progressive Retinal Atrophy (Abyssinian Type)
WT/WT
Normal (Clear)
Progressive Retinal Atrophy (Bengal Type)
WT/WT
Normal (Clear)
Progressive Retinal Atrophy (Persian Type)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Vitamin D-Dependent Rickets Type IB
WT/WT
Normal (Clear)
Vitamin D-dependent Rickets, Type IA, Variant 1
WT/WT
Normal (Clear)
Vitamin D-dependent Rickets, Type IA, Variant 2
WT/WT
Normal (Clear)
F1 Dragon of KingSavannahs
Dragon is still young but has the heart of an elder. She is cautious and wise. Her beauty is aparent and we cannot wait to see her continue to grow!Â
F1 IWannaSavannah Neytiri of KingSavannahs
Neytiri is an absolute sweetheart and teaches her babies to be gentle and love everyone including dogs and other cats. She is extremely intelligent and a stunning looking girl. Naytiri is a melanistic carrier.Â
Neytiri's disease testing resultsÂ
Disease Name
Genotype
Interpretation
Acute Intermittent Porphyria, Variant 1
WT/WT
Normal (Clear)
Acute Intermittent Porphyria, Variant 2
WT/WT
Normal (Clear)
Acute Intermittent Porphyria, Variant 3
WT/WT
Normal (Clear)
Acute Intermittent Porphyria, Variant 4 (Siamese Type 1)
WT/WT
Normal (Clear)
Acute Intermittent Porphyria, Variant 5 (Siamese Type 2)
WT/WT
Normal (Clear)
Acute Intermittent Porphyria, Variant 6
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Autoimmune Lymphoproliferative Syndrome
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Congenital Adrenal Hyperplasia
WT/WT
Normal (Clear)
Congenital Erythropoietic Porphyria, Variant 1
WT/WT
Normal (Clear)
Congenital Erythropoietic Porphyria, Variant 2
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Congenital Myasthenic Syndrome
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
No Result
No Result
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Dihydropyrimidinase Deficiency
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Factor XII Deficiency, Variant 1
WT/WT
Normal (Clear)
Factor XII Deficiency, Variant 2
WT/WT
Normal (Clear)
Factor XII Deficiency, Variant 3
WT/WT
Normal (Clear)
Feline Immunodeficiency Virus (FIV) Infection Risk Modifier
WT/WT
No Increased Resistance to FIV Infection
Feline Leukocyte Adhesion Deficiency, Type 1
No Result
No Result
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Forebrain Commissural Malformation
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Glycogen Storage Disease, Type IV
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
GM2 Gangliosidosis, Type II (Burmese Type)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
GM2 Gangliosidosis, Type II (Japanese Domestic Type)
WT/WT
Normal (Clear)
GM2 Gangliosidosis, Type II (Korat Type)
WT/WT
Normal (Clear)
WT/WT
X-Linked Female Normal
WT/WT
X-Linked Female Normal
WT/WT
Normal (Clear)
Hypertrophic Cardiomyopathy (Maine Coon Type)
WT/WT
Normal (Clear)
Hypertrophic Cardiomyopathy (Ragdoll Type)
WT/WT
Normal (Clear)
Hypertrophic Cardiomyopathy (Sphynx Type Risk Factor)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Hypokalemic Periodic Paralysis
WT/WT
Normal (Clear)
Hypotrichosis with Short Life Expectancy
WT/WT
Normal (Clear)
Inflammatory Linear Verrucous Epidermal Nevus
WT/WT
X-Linked Female Normal
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Mucopolysaccharidosis Type VI (Modifier)
WT/WT
Normal (Clear)
Mucopolysaccharidosis Type VI (Siamese Type)
WT/WT
Normal (Clear)
Mucopolysaccharidosis Type VII, Variant 1
WT/WT
Normal (Clear)
Mucopolysaccharidosis Type VII, Variant 2
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Neuronal Ceroid Lipofuscinosis 6
WT/WT
Normal (Clear)
Neuronal Ceroid Lipofuscinosis 7, Variant 1
WT/WT
Normal (Clear)
Neuronal Ceroid Lipofuscinosis 7, Variant 2
WT/WT
Normal (Clear)
Niemann-Pick C1 Disease, Variant 1
WT/WT
Normal (Clear)
Niemann-Pick C1 Disease, Variant 2
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Polycystic Kidney Disease (Siberian Type)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Progressive Retinal Atrophy (Abyssinian Type)
WT/WT
Normal (Clear)
Progressive Retinal Atrophy (Bengal Type)
WT/WT
Normal (Clear)
Progressive Retinal Atrophy (Persian Type)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Vitamin D-Dependent Rickets Type IB
WT/WT
Normal (Clear)
Vitamin D-dependent Rickets, Type IA, Variant 1
WT/WT
Normal (Clear)
Vitamin D-dependent Rickets, Type IA, Variant 2
WT/WT
Normal (Clear)
F1 Drinkwater MarhyaÂ
of KingSavannahs
Marhya is a quiet love. She is the peacekeeper of the group and waits for an invitation for attention. Her favorite place is the foot of the bed, and anywhere in the sunshine. She produced the stunning F2 baby Charlie.Â
Marhyas disease testing resultsÂ
Disease Name
Genotype
Interpretation
Acute Intermittent Porphyria, Variant 1
WT/WT
Normal (clear)
Acute Intermittent Porphyria, Variant 2
WT/WT
Normal (clear)
Acute Intermittent Porphyria, Variant 3
WT/WT
Normal (clear)
Acute Intermittent Porphyria, Variant 4 (Siamese Type 1)
WT/WT
Normal (clear)
Acute Intermittent Porphyria, Variant 5 (Siamese Type 2)
WT/WT
Normal (clear)
Acute Intermittent Porphyria, Variant 6
WT/WT
Normal (clear)
Autoimmune Lymphoproliferative Syndrome
WT/WT
Normal (clear)
WT/WT
Normal (clear)
Congenital Adrenal Hyperplasia
WT/WT
Normal (clear)
Congenital Erythropoietic Porphyria, Variant 1
WT/WT
Normal (clear)
Congenital Erythropoietic Porphyria, Variant 2
WT/WT
Normal (clear)
WT/WT
Normal (clear)
Congenital Myasthenic Syndrome
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
Dihydropyrimidinase Deficiency
WT/WT
Normal (clear)
Factor XII Deficiency, Variant 1
WT/WT
Normal (clear)
Feline Leukocyte Adhesion Deficiency, Type 1
No Result
No Result
WT/WT
Normal (clear)
Glycogen Storage Disease, Type IV
WT/WT
Normal (clear)
WT/WT
Normal (clear)
GM2 Gangliosidosis, Type II (Burmese Type)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
GM2 Gangliosidosis, Type II (Japanese Domestic Type)
WT/WT
Normal (clear)
GM2 Gangliosidosis, Type II (Korat Type)
WT/WT
Normal (clear)
WT/WT
X-Linked Female Normal
WT/WT
X-Linked Female Normal
WT/WT
Normal (clear)
Hypertrophic Cardiomyopathy (Maine Coon Type)
WT/WT
Normal (clear)
Hypertrophic Cardiomyopathy (Ragdoll Type)
WT/WT
Normal (clear)
Hypokalemic Periodic Paralysis
WT/WT
Normal (clear)
Hypotrichosis with Short Life Expectancy
WT/WT
Normal (clear)
WT/WT
Normal (clear)
Mucopolysaccharidosis Type VI (Modifier)
WT/WT
Normal (clear)
Mucopolysaccharidosis Type VI (Siamese Type)
WT/WT
Normal (clear)
Mucopolysaccharidosis Type VII, Variant 1
WT/WT
Normal (clear)
Mucopolysaccharidosis Type VII, Variant 2
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
Niemann-Pick C1 Disease, Variant 1
WT/WT
Normal (clear)
Niemann-Pick C1 Disease, Variant 2
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
Progressive Retinal Atrophy (Abyssinian Type)
WT/WT
Normal (clear)
Progressive Retinal Atrophy (Persian Type)
WT/WT
Normal (clear)
M/M
At-Risk
WT/WT
Normal (clear)
Vitamin D-dependent Rickets, Type IA, Variant 1
WT/WT
Normal (clear)
Vitamin D-dependent Rickets, Type IA, Variant 2
WT/WT
Normal (clear)
F1 Dreamkatzexotic Pandora
Pandora is a fireball and still shows her young energy. She will play all day long and loves MIssy (They all havve their favorites). Panda's wild look and black nose demands attention.
Pandoras disease testing results
Disease Name
Genotype
Interpretation
Acute Intermittent Porphyria, Variant 1
WT/WT
Normal (Clear)
Acute Intermittent Porphyria, Variant 2
WT/WT
Normal (Clear)
Acute Intermittent Porphyria, Variant 3
WT/WT
Normal (Clear)
Acute Intermittent Porphyria, Variant 4 (Siamese Type 1)
WT/WT
Normal (Clear)
Acute Intermittent Porphyria, Variant 5 (Siamese Type 2)
WT/WT
Normal (Clear)
Acute Intermittent Porphyria, Variant 6
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Autoimmune Lymphoproliferative Syndrome
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Congenital Adrenal Hyperplasia
WT/WT
Normal (Clear)
Congenital Erythropoietic Porphyria, Variant 1
WT/WT
Normal (Clear)
Congenital Erythropoietic Porphyria, Variant 2
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Congenital Myasthenic Syndrome
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Dihydropyrimidinase Deficiency
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Factor XII Deficiency, Variant 1
WT/WT
Normal (Clear)
Factor XII Deficiency, Variant 2
WT/WT
Normal (Clear)
Factor XII Deficiency, Variant 3
WT/WT
Normal (Clear)
Feline Immunodeficiency Virus (FIV) Infection Risk Modifier
WT/WT
No Increased Resistance to FIV Infection
Feline Leukocyte Adhesion Deficiency, Type 1
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Forebrain Commissural Malformation
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Glycogen Storage Disease, Type IV
WT/WT
Normal (Clear)
GM2 Gangliosidosis, Type II (Burmese Type)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
GM2 Gangliosidosis, Type II (Japanese Domestic Type)
WT/WT
Normal (Clear)
GM2 Gangliosidosis, Type II (Korat Type)
WT/WT
Normal (Clear)
WT/WT
X-Linked Female Normal
WT/WT
X-Linked Female Normal
WT/WT
Normal (Clear)
Hypertrophic Cardiomyopathy (Maine Coon Type)
WT/WT
Normal (Clear)
Hypertrophic Cardiomyopathy (Ragdoll Type)
WT/WT
Normal (Clear)
Hypertrophic Cardiomyopathy (Sphynx Type Risk Factor)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Hypokalemic Periodic Paralysis
WT/WT
Normal (Clear)
Hypotrichosis with Short Life Expectancy
WT/WT
Normal (Clear)
Inflammatory Linear Verrucous Epidermal Nevus
WT/WT
X-Linked Female Normal
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Mucopolysaccharidosis Type VI (Modifier)
WT/WT
Normal (Clear)
Mucopolysaccharidosis Type VI (Siamese Type)
WT/WT
Normal (Clear)
Mucopolysaccharidosis Type VII, Variant 1
WT/WT
Normal (Clear)
Mucopolysaccharidosis Type VII, Variant 2
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Neuronal Ceroid Lipofuscinosis 6
WT/WT
Normal (Clear)
Neuronal Ceroid Lipofuscinosis 7, Variant 1
WT/WT
Normal (Clear)
Neuronal Ceroid Lipofuscinosis 7, Variant 2
WT/WT
Normal (Clear)
Niemann-Pick C1 Disease, Variant 1
WT/WT
Normal (Clear)
Niemann-Pick C1 Disease, Variant 2
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Polycystic Kidney Disease (Siberian Type)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Progressive Retinal Atrophy (Abyssinian Type)
WT/WT
Normal (Clear)
Progressive Retinal Atrophy (Bengal Type)
WT/WT
Normal (Clear)
Progressive Retinal Atrophy (Persian Type)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Vitamin D-Dependent Rickets Type IB
WT/WT
Normal (Clear)
Vitamin D-dependent Rickets, Type IA, Variant 1
WT/WT
Normal (Clear)
Vitamin D-dependent Rickets, Type IA, Variant 2
WT/WT
Normal (Clear)
F2 KingSavannahs CharlieÂ
Charlie was born at King Savannahs and we are so proud of her! She is curious and mischievous which keeps us on our toes! Her knowing look and young confidence is sure to strengthen as she gets older.Â
F3 KingSavannahs Invisible Igboo
Iggy is the spoiled one who wants all the attention. She demands attention and is expecting royal treatment. Iggy is a friend to all.Â
SBT HarmonySavannah Khaleesi of KingSavannahs
Khaleesi is the TikTok famous Snow Spotted Savannah. Her stunning big blue eyes and elegant demeanor is hard not to love. She is the queen that produces HUGE F6 males, growing over 20 pounds.Â
Khaleesi's disease testing resultsÂ
Disease Name
Genotype
Interpretation
Acute Intermittent Porphyria, Variant 1
WT/WT
Normal (clear)
Acute Intermittent Porphyria, Variant 2
WT/WT
Normal (clear)
Acute Intermittent Porphyria, Variant 3
WT/WT
Normal (clear)
Acute Intermittent Porphyria, Variant 4 (Siamese Type 1)
WT/WT
Normal (clear)
Acute Intermittent Porphyria, Variant 5 (Siamese Type 2)
WT/WT
Normal (clear)
Acute Intermittent Porphyria, Variant 6
WT/WT
Normal (clear)
Autoimmune Lymphoproliferative Syndrome
WT/WT
Normal (clear)
WT/WT
Normal (clear)
Congenital Adrenal Hyperplasia
WT/WT
Normal (clear)
Congenital Erythropoietic Porphyria, Variant 1
WT/WT
Normal (clear)
Congenital Erythropoietic Porphyria, Variant 2
WT/WT
Normal (clear)
WT/WT
Normal (clear)
Congenital Myasthenic Syndrome
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
Dihydropyrimidinase Deficiency
WT/WT
Normal (clear)
Factor XII Deficiency, Variant 1
WT/WT
Normal (clear)
Feline Leukocyte Adhesion Deficiency, Type 1
WT/WT
Normal (clear)
WT/WT
Normal (clear)
Glycogen Storage Disease, Type IV
WT/WT
Normal (clear)
WT/WT
Normal (clear)
GM2 Gangliosidosis, Type II (Burmese Type)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
GM2 Gangliosidosis, Type II (Japanese Domestic Type)
WT/WT
Normal (clear)
GM2 Gangliosidosis, Type II (Korat Type)
WT/WT
Normal (clear)
WT/WT
X-Linked Female Normal
WT/WT
X-Linked Female Normal
WT/WT
Normal (clear)
Hypertrophic Cardiomyopathy (Maine Coon Type)
WT/WT
Normal (clear)
Hypertrophic Cardiomyopathy (Ragdoll Type)
WT/WT
Normal (clear)
Hypokalemic Periodic Paralysis
WT/WT
Normal (clear)
Hypotrichosis with Short Life Expectancy
WT/WT
Normal (clear)
WT/WT
Normal (clear)
Mucopolysaccharidosis Type VI (Modifier)
WT/WT
Normal (clear)
Mucopolysaccharidosis Type VI (Siamese Type)
WT/WT
Normal (clear)
Mucopolysaccharidosis Type VII, Variant 1
WT/WT
Normal (clear)
Mucopolysaccharidosis Type VII, Variant 2
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
Niemann-Pick C1 Disease, Variant 1
WT/WT
Normal (clear)
Niemann-Pick C1 Disease, Variant 2
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
Progressive Retinal Atrophy (Abyssinian Type)
WT/WT
Normal (clear)
Progressive Retinal Atrophy (Persian Type)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
Vitamin D-dependent Rickets, Type IA, Variant 1
WT/WT
Normal (clear)
Vitamin D-dependent Rickets, Type IA, Variant 2
WT/WT
Normal (clear)
SBT DixieDots Yankee of KingSavannahs
Yankee is the momma bear of the group. She is not only the best mother to her own kittens but is the one who will take in ANY baby. She has raised many babies for others and teaches them to be loving and gentle. Yankee is the GOAT.
Yankee's disease testing results
Disease Name
Genotype
Interpretation
Acute Intermittent Porphyria, Variant 1
WT/WT
Normal (clear)
Acute Intermittent Porphyria, Variant 2
WT/WT
Normal (clear)
Acute Intermittent Porphyria, Variant 3
WT/WT
Normal (clear)
Acute Intermittent Porphyria, Variant 4 (Siamese Type 1)
WT/WT
Normal (clear)
Acute Intermittent Porphyria, Variant 5 (Siamese Type 2)
WT/WT
Normal (clear)
Acute Intermittent Porphyria, Variant 6
WT/WT
Normal (clear)
Autoimmune Lymphoproliferative Syndrome
WT/WT
Normal (clear)
WT/WT
Normal (clear)
Congenital Adrenal Hyperplasia
WT/WT
Normal (clear)
Congenital Erythropoietic Porphyria, Variant 1
WT/WT
Normal (clear)
Congenital Erythropoietic Porphyria, Variant 2
WT/WT
Normal (clear)
WT/WT
Normal (clear)
Congenital Myasthenic Syndrome
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
Dihydropyrimidinase Deficiency
WT/WT
Normal (clear)
Factor XII Deficiency, Variant 1
WT/WT
Normal (clear)
Feline Leukocyte Adhesion Deficiency, Type 1
WT/WT
Normal (clear)
WT/WT
Normal (clear)
Glycogen Storage Disease, Type IV
WT/WT
Normal (clear)
WT/WT
Normal (clear)
GM2 Gangliosidosis, Type II (Burmese Type)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
GM2 Gangliosidosis, Type II (Japanese Domestic Type)
WT/WT
Normal (clear)
GM2 Gangliosidosis, Type II (Korat Type)
WT/WT
Normal (clear)
WT/WT
X-Linked Female Normal
WT/WT
X-Linked Female Normal
WT/WT
Normal (clear)
Hypertrophic Cardiomyopathy (Maine Coon Type)
WT/WT
Normal (clear)
Hypertrophic Cardiomyopathy (Ragdoll Type)
WT/WT
Normal (clear)
Hypokalemic Periodic Paralysis
WT/WT
Normal (clear)
Hypotrichosis with Short Life Expectancy
WT/WT
Normal (clear)
WT/WT
Normal (clear)
Mucopolysaccharidosis Type VI (Modifier)
WT/WT
Normal (clear)
Mucopolysaccharidosis Type VI (Siamese Type)
WT/WT
Normal (clear)
Mucopolysaccharidosis Type VII, Variant 1
WT/WT
Normal (clear)
Mucopolysaccharidosis Type VII, Variant 2
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
Niemann-Pick C1 Disease, Variant 1
WT/WT
Normal (clear)
Niemann-Pick C1 Disease, Variant 2
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
Progressive Retinal Atrophy (Abyssinian Type)
WT/WT
Normal (clear)
Progressive Retinal Atrophy (Persian Type)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
WT/WT
Normal (clear)
Vitamin D-dependent Rickets, Type IA, Variant 1
WT/WT
Normal (clear)
Vitamin D-dependent Rickets, Type IA, Variant 2
WT/WT
Normal (clear)
SBT KingSavannahs Nanny Bird
Nanny Bird got her name as a teen kitten because she would "babysit" all the babies when their moms would take a break and leave the room. She is extremely gentle and allows young kittens to climb and play with her. She has proven to produce stunning babies with impressive spots and ears. She is also a carrier of the rare (but GREAT) FIV resistance gene, which she passes to her kittens.Â
Nanny's disease testing resultsÂ
Disease Name
Genotype
Interpretation
Acute Intermittent Porphyria, Variant 1
WT/WT
Normal (Clear)
Acute Intermittent Porphyria, Variant 2
WT/WT
Normal (Clear)
Acute Intermittent Porphyria, Variant 3
WT/WT
Normal (Clear)
Acute Intermittent Porphyria, Variant 4 (Siamese Type 1)
WT/WT
Normal (Clear)
Acute Intermittent Porphyria, Variant 5 (Siamese Type 2)
WT/WT
Normal (Clear)
Acute Intermittent Porphyria, Variant 6
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Autoimmune Lymphoproliferative Syndrome
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Congenital Adrenal Hyperplasia
WT/WT
Normal (Clear)
Congenital Erythropoietic Porphyria, Variant 1
WT/WT
Normal (Clear)
Congenital Erythropoietic Porphyria, Variant 2
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Congenital Myasthenic Syndrome
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Dihydropyrimidinase Deficiency
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Factor XII Deficiency, Variant 1
WT/WT
Normal (Clear)
Factor XII Deficiency, Variant 2
WT/M
Carrier
Factor XII Deficiency, Variant 3
WT/WT
Normal (Clear)
Feline Immunodeficiency Virus (FIV) Infection Risk Modifier
WT/M
Increased Resistance to FIV Infection
Feline Leukocyte Adhesion Deficiency, Type 1
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Forebrain Commissural Malformation
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Glycogen Storage Disease, Type IV
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
GM2 Gangliosidosis, Type II (Burmese Type)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
GM2 Gangliosidosis, Type II (Japanese Domestic Type)
WT/WT
Normal (Clear)
GM2 Gangliosidosis, Type II (Korat Type)
WT/WT
Normal (Clear)
WT/WT
X-Linked Female Normal
WT/WT
X-Linked Female Normal
WT/WT
Normal (Clear)
Hypertrophic Cardiomyopathy (Maine Coon Type)
WT/WT
Normal (Clear)
Hypertrophic Cardiomyopathy (Ragdoll Type)
WT/WT
Normal (Clear)
Hypertrophic Cardiomyopathy (Sphynx Type Risk Factor)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Hypokalemic Periodic Paralysis
WT/WT
Normal (Clear)
Hypotrichosis with Short Life Expectancy
WT/WT
Normal (Clear)
Inflammatory Linear Verrucous Epidermal Nevus
WT/WT
X-Linked Female Normal
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Mucopolysaccharidosis Type VI (Modifier)
WT/WT
Normal (Clear)
Mucopolysaccharidosis Type VI (Siamese Type)
WT/WT
Normal (Clear)
Mucopolysaccharidosis Type VII, Variant 1
WT/WT
Normal (Clear)
Mucopolysaccharidosis Type VII, Variant 2
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Neuronal Ceroid Lipofuscinosis 6
WT/WT
Normal (Clear)
Neuronal Ceroid Lipofuscinosis 7, Variant 1
No Result
No Result
Neuronal Ceroid Lipofuscinosis 7, Variant 2
WT/WT
Normal (Clear)
Niemann-Pick C1 Disease, Variant 1
WT/WT
Normal (Clear)
Niemann-Pick C1 Disease, Variant 2
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Polycystic Kidney Disease (Siberian Type)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Progressive Retinal Atrophy (Abyssinian Type)
WT/WT
Normal (Clear)
Progressive Retinal Atrophy (Bengal Type)
WT/WT
Normal (Clear)
Progressive Retinal Atrophy (Persian Type)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
WT/WT
Normal (Clear)
Vitamin D-Dependent Rickets Type IB
WT/WT
Normal (Clear)
Vitamin D-dependent Rickets, Type IA, Variant 1
WT/WT
Normal (Clear)
Vitamin D-dependent Rickets, Type IA, Variant 2
WT/WT
Normal (Clear)