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. 

Bala's disease testing results 

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)

Brachycephaly (Burmese Type)

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)

Congenital Hypothyroidism

WT/WT

Normal (clear)

Congenital Myasthenic Syndrome

WT/WT

Normal (clear)

Cystinuria, Type 1A

WT/WT

Normal (clear)

Cystinuria, Type B, Variant 1

No Result

No Result

Cystinuria, Type B, Variant 2

WT/WT

Normal (clear)

Cystinuria, Type B, Variant 3

WT/WT

Normal (clear)

Cystinuria, Type B, Variant 4

WT/WT

Normal (clear)

Cystinuria, Type B, Variant 5

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)

Gangliosidosis GM2A

WT/WT

Normal (clear)

Glycogen Storage Disease, Type IV

WT/WT

Normal (clear)

GM1 Gangliosidosis

WT/WT

Normal (clear)

GM2 Gangliosidosis, Type II (Burmese Type)

WT/WT

Normal (clear)

GM2 Gangliosidosis, Type II

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)

Hemophilia B, Variant 1

WT/WT

X-Linked Female Normal

Hemophilia B, Variant 2

WT/WT

X-Linked Female Normal

Hyperlipoproteinemia

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)

Mucopolysaccharidosis Type I

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)

Multiple Drug Resistance

WT/WT

Normal (clear)

Myotonia Congenita

No Result

No Result

Niemann-Pick C1 Disease, Variant 1

WT/WT

Normal (clear)

Niemann-Pick C1 Disease, Variant 2

WT/WT

Normal (clear)

Niemann-Pick C2 Disease

WT/WT

Normal (clear)

Polycystic Kidney Disease

WT/WT

Normal (clear)

Primary Hyperoxaluria Type II

WT/WT

Normal (clear)

Progressive Retinal Atrophy (Abyssinian Type)

WT/WT

Normal (clear)

Progressive Retinal Atrophy (Persian Type)

WT/WT

Normal (clear)

Pyruvate Kinase Deficiency

WT/WT

Normal (clear)

Spinal Muscular Atrophy

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 results 

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)

Alpha Mannosidosis

WT/WT

Normal (Clear)

Autoimmune Lymphoproliferative Syndrome

WT/WT

Normal (Clear)

Brachycephaly (Burmese Type)

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)

Congenital Hypothyroidism

WT/WT

Normal (Clear)

Congenital Myasthenic Syndrome

WT/WT

Normal (Clear)

Cystinuria, Type 1A

WT/WT

Normal (Clear)

Cystinuria, Type B, Variant 1

WT/WT

Normal (Clear)

Cystinuria, Type B, Variant 2

WT/WT

Normal (Clear)

Cystinuria, Type B, Variant 3

WT/WT

Normal (Clear)

Cystinuria, Type B, Variant 4

WT/WT

Normal (Clear)

Cystinuria, Type B, Variant 5

WT/WT

Normal (Clear)

Dihydropyrimidinase Deficiency

WT/WT

Normal (Clear)

Epidermolysis Bullosa Simplex

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)

Feline Niemann-Pick Disease

WT/WT

Normal (Clear)

Feline Spongy Encephalopathy

WT/WT

Normal (Clear)

Forebrain Commissural Malformation

WT/WT

Normal (Clear)

Gangliosidosis GM2A

WT/WT

Normal (Clear)

Glycogen Storage Disease, Type IV

WT/WT

Normal (Clear)

GM1 Gangliosidosis

WT/WT

Normal (Clear)

GM2 Gangliosidosis, Type II (Burmese Type)

WT/WT

Normal (Clear)

GM2 Gangliosidosis, Type II

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)

Hemophilia B, Variant 1

WT/WT

X-Linked Female Normal

Hemophilia B, Variant 2

WT/WT

X-Linked Female Normal

Hyperlipoproteinemia

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)

Hypogonadotropic Hypogonadism

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

L-2-Hydroxyglutaric Aciduria

WT/WT

Normal (Clear)

Methemoglobinemia, Variant 1

WT/WT

Normal (Clear)

Methemoglobinemia, Variant 2

WT/WT

Normal (Clear)

Mucolipidosis II

WT/WT

Normal (Clear)

Mucopolysaccharidosis Type I

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)

Multiple Drug Resistance

WT/WT

Normal (Clear)

Myotonia Congenita

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)

Niemann-Pick C2 Disease

WT/WT

Normal (Clear)

Oculocutaneous Albinism

WT/WT

Normal (Clear)

Polycystic Kidney Disease

WT/WT

Normal (Clear)

Polycystic Kidney Disease (Siberian Type)

WT/WT

Normal (Clear)

Primary Congenital Glaucoma

WT/WT

Normal (Clear)

Primary Hyperoxaluria Type II

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)

Pyruvate Kinase Deficiency

WT/WT

Normal (Clear)

Rod-Cone Dysplasia

WT/WT

Normal (Clear)

Spinal Muscular Atrophy

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! 

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. 

Neytiri'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)

Alpha Mannosidosis

WT/WT

Normal (Clear)

Autoimmune Lymphoproliferative Syndrome

WT/WT

Normal (Clear)

Brachycephaly (Burmese Type)

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)

Congenital Hypothyroidism

WT/WT

Normal (Clear)

Congenital Myasthenic Syndrome

WT/WT

Normal (Clear)

Cystinuria, Type 1A

WT/WT

Normal (Clear)

Cystinuria, Type B, Variant 1

No Result

No Result

Cystinuria, Type B, Variant 2

WT/WT

Normal (Clear)

Cystinuria, Type B, Variant 3

WT/WT

Normal (Clear)

Cystinuria, Type B, Variant 4

WT/WT

Normal (Clear)

Cystinuria, Type B, Variant 5

WT/WT

Normal (Clear)

Dihydropyrimidinase Deficiency

WT/WT

Normal (Clear)

Epidermolysis Bullosa Simplex

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

Feline Niemann-Pick Disease

WT/WT

Normal (Clear)

Feline Spongy Encephalopathy

WT/WT

Normal (Clear)

Forebrain Commissural Malformation

WT/WT

Normal (Clear)

Gangliosidosis GM2A

WT/WT

Normal (Clear)

Glycogen Storage Disease, Type IV

WT/WT

Normal (Clear)

GM1 Gangliosidosis

WT/WT

Normal (Clear)

GM2 Gangliosidosis, Type II (Burmese Type)

WT/WT

Normal (Clear)

GM2 Gangliosidosis, Type II

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)

Hemophilia B, Variant 1

WT/WT

X-Linked Female Normal

Hemophilia B, Variant 2

WT/WT

X-Linked Female Normal

Hyperlipoproteinemia

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)

Hypogonadotropic Hypogonadism

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

L-2-Hydroxyglutaric Aciduria

WT/WT

Normal (Clear)

Methemoglobinemia, Variant 1

WT/WT

Normal (Clear)

Methemoglobinemia, Variant 2

WT/WT

Normal (Clear)

Mucolipidosis II

WT/WT

Normal (Clear)

Mucopolysaccharidosis Type I

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)

Multiple Drug Resistance

WT/WT

Normal (Clear)

Myotonia Congenita

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)

Niemann-Pick C2 Disease

WT/WT

Normal (Clear)

Oculocutaneous Albinism

WT/WT

Normal (Clear)

Polycystic Kidney Disease

WT/WT

Normal (Clear)

Polycystic Kidney Disease (Siberian Type)

WT/WT

Normal (Clear)

Primary Congenital Glaucoma

WT/WT

Normal (Clear)

Primary Hyperoxaluria Type II

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)

Pyruvate Kinase Deficiency

WT/WT

Normal (Clear)

Rod-Cone Dysplasia

WT/WT

Normal (Clear)

Spinal Muscular Atrophy

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 Marhya 

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. 

Marhyas 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)

Brachycephaly (Burmese Type)

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)

Congenital Hypothyroidism

WT/WT

Normal (clear)

Congenital Myasthenic Syndrome

WT/WT

Normal (clear)

Cystinuria, Type 1A

WT/WT

Normal (clear)

Cystinuria, Type B, Variant 1

WT/WT

Normal (clear)

Cystinuria, Type B, Variant 2

WT/WT

Normal (clear)

Cystinuria, Type B, Variant 3

WT/WT

Normal (clear)

Cystinuria, Type B, Variant 4

WT/WT

Normal (clear)

Cystinuria, Type B, Variant 5

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

Gangliosidosis GM2A

WT/WT

Normal (clear)

Glycogen Storage Disease, Type IV

WT/WT

Normal (clear)

GM1 Gangliosidosis

WT/WT

Normal (clear)

GM2 Gangliosidosis, Type II (Burmese Type)

WT/WT

Normal (clear)

GM2 Gangliosidosis, Type II

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)

Hemophilia B, Variant 1

WT/WT

X-Linked Female Normal

Hemophilia B, Variant 2

WT/WT

X-Linked Female Normal

Hyperlipoproteinemia

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)

Mucopolysaccharidosis Type I

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)

Multiple Drug Resistance

WT/WT

Normal (clear)

Myotonia Congenita

WT/WT

Normal (clear)

Niemann-Pick C1 Disease, Variant 1

WT/WT

Normal (clear)

Niemann-Pick C1 Disease, Variant 2

WT/WT

Normal (clear)

Niemann-Pick C2 Disease

WT/WT

Normal (clear)

Polycystic Kidney Disease

WT/WT

Normal (clear)

Primary Hyperoxaluria Type II

WT/WT

Normal (clear)

Progressive Retinal Atrophy (Abyssinian Type)

WT/WT

Normal (clear)

Progressive Retinal Atrophy (Persian Type)

WT/WT

Normal (clear)

Pyruvate Kinase Deficiency

M/M

At-Risk

Spinal Muscular Atrophy

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)

Alpha Mannosidosis

WT/WT

Normal (Clear)

Autoimmune Lymphoproliferative Syndrome

WT/WT

Normal (Clear)

Brachycephaly (Burmese Type)

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)

Congenital Hypothyroidism

WT/WT

Normal (Clear)

Congenital Myasthenic Syndrome

WT/WT

Normal (Clear)

Cystinuria, Type 1A

WT/WT

Normal (Clear)

Cystinuria, Type B, Variant 2

WT/WT

Normal (Clear)

Cystinuria, Type B, Variant 3

WT/WT

Normal (Clear)

Cystinuria, Type B, Variant 4

WT/WT

Normal (Clear)

Cystinuria, Type B, Variant 5

WT/WT

Normal (Clear)

Dihydropyrimidinase Deficiency

WT/WT

Normal (Clear)

Epidermolysis Bullosa Simplex

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)

Feline Niemann-Pick Disease

WT/WT

Normal (Clear)

Feline Spongy Encephalopathy

WT/WT

Normal (Clear)

Forebrain Commissural Malformation

WT/WT

Normal (Clear)

Gangliosidosis GM2A

WT/WT

Normal (Clear)

Glycogen Storage Disease, Type IV

WT/WT

Normal (Clear)

GM2 Gangliosidosis, Type II (Burmese Type)

WT/WT

Normal (Clear)

GM2 Gangliosidosis, Type II

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)

Hemophilia B, Variant 1

WT/WT

X-Linked Female Normal

Hemophilia B, Variant 2

WT/WT

X-Linked Female Normal

Hyperlipoproteinemia

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)

Hypogonadotropic Hypogonadism

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

L-2-Hydroxyglutaric Aciduria

WT/WT

Normal (Clear)

Methemoglobinemia, Variant 1

WT/WT

Normal (Clear)

Methemoglobinemia, Variant 2

WT/WT

Normal (Clear)

Mucolipidosis II

WT/WT

Normal (Clear)

Mucopolysaccharidosis Type I

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)

Multiple Drug Resistance

WT/WT

Normal (Clear)

Myotonia Congenita

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)

Niemann-Pick C2 Disease

WT/WT

Normal (Clear)

Oculocutaneous Albinism

WT/WT

Normal (Clear)

Polycystic Kidney Disease

WT/WT

Normal (Clear)

Polycystic Kidney Disease (Siberian Type)

WT/WT

Normal (Clear)

Primary Congenital Glaucoma

WT/WT

Normal (Clear)

Primary Hyperoxaluria Type II

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)

Pyruvate Kinase Deficiency

WT/WT

Normal (Clear)

Rod-Cone Dysplasia

WT/WT

Normal (Clear)

Spinal Muscular Atrophy

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 Charlie 

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. 

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. 

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. 

Khaleesi'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)

Brachycephaly (Burmese Type)

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)

Congenital Hypothyroidism

WT/WT

Normal (clear)

Congenital Myasthenic Syndrome

WT/WT

Normal (clear)

Cystinuria, Type 1A

WT/WT

Normal (clear)

Cystinuria, Type B, Variant 1

WT/WT

Normal (clear)

Cystinuria, Type B, Variant 2

WT/WT

Normal (clear)

Cystinuria, Type B, Variant 3

WT/WT

Normal (clear)

Cystinuria, Type B, Variant 4

WT/WT

Normal (clear)

Cystinuria, Type B, Variant 5

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)

Gangliosidosis GM2A

WT/WT

Normal (clear)

Glycogen Storage Disease, Type IV

WT/WT

Normal (clear)

GM1 Gangliosidosis

WT/WT

Normal (clear)

GM2 Gangliosidosis, Type II (Burmese Type)

WT/WT

Normal (clear)

GM2 Gangliosidosis, Type II

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)

Hemophilia B, Variant 1

WT/WT

X-Linked Female Normal

Hemophilia B, Variant 2

WT/WT

X-Linked Female Normal

Hyperlipoproteinemia

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)

Mucopolysaccharidosis Type I

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)

Multiple Drug Resistance

WT/WT

Normal (clear)

Myotonia Congenita

WT/WT

Normal (clear)

Niemann-Pick C1 Disease, Variant 1

WT/WT

Normal (clear)

Niemann-Pick C1 Disease, Variant 2

WT/WT

Normal (clear)

Niemann-Pick C2 Disease

WT/WT

Normal (clear)

Polycystic Kidney Disease

WT/WT

Normal (clear)

Primary Hyperoxaluria Type II

WT/WT

Normal (clear)

Progressive Retinal Atrophy (Abyssinian Type)

WT/WT

Normal (clear)

Progressive Retinal Atrophy (Persian Type)

WT/WT

Normal (clear)

Pyruvate Kinase Deficiency

WT/WT

Normal (clear)

Spinal Muscular Atrophy

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)

Brachycephaly (Burmese Type)

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)

Congenital Hypothyroidism

WT/WT

Normal (clear)

Congenital Myasthenic Syndrome

WT/WT

Normal (clear)

Cystinuria, Type 1A

WT/WT

Normal (clear)

Cystinuria, Type B, Variant 1

WT/WT

Normal (clear)

Cystinuria, Type B, Variant 2

WT/WT

Normal (clear)

Cystinuria, Type B, Variant 3

WT/WT

Normal (clear)

Cystinuria, Type B, Variant 4

WT/WT

Normal (clear)

Cystinuria, Type B, Variant 5

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)

Gangliosidosis GM2A

WT/WT

Normal (clear)

Glycogen Storage Disease, Type IV

WT/WT

Normal (clear)

GM1 Gangliosidosis

WT/WT

Normal (clear)

GM2 Gangliosidosis, Type II (Burmese Type)

WT/WT

Normal (clear)

GM2 Gangliosidosis, Type II

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)

Hemophilia B, Variant 1

WT/WT

X-Linked Female Normal

Hemophilia B, Variant 2

WT/WT

X-Linked Female Normal

Hyperlipoproteinemia

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)

Mucopolysaccharidosis Type I

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)

Multiple Drug Resistance

WT/WT

Normal (clear)

Myotonia Congenita

WT/WT

Normal (clear)

Niemann-Pick C1 Disease, Variant 1

WT/WT

Normal (clear)

Niemann-Pick C1 Disease, Variant 2

WT/WT

Normal (clear)

Niemann-Pick C2 Disease

WT/WT

Normal (clear)

Polycystic Kidney Disease

WT/WT

Normal (clear)

Primary Hyperoxaluria Type II

WT/WT

Normal (clear)

Progressive Retinal Atrophy (Abyssinian Type)

WT/WT

Normal (clear)

Progressive Retinal Atrophy (Persian Type)

WT/WT

Normal (clear)

Pyruvate Kinase Deficiency

WT/WT

Normal (clear)

Spinal Muscular Atrophy

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. 

Nanny'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)

Alpha Mannosidosis

WT/WT

Normal (Clear)

Autoimmune Lymphoproliferative Syndrome

WT/WT

Normal (Clear)

Brachycephaly (Burmese Type)

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)

Congenital Hypothyroidism

WT/WT

Normal (Clear)

Congenital Myasthenic Syndrome

WT/WT

Normal (Clear)

Cystinuria, Type 1A

WT/WT

Normal (Clear)

Cystinuria, Type B, Variant 1

WT/WT

Normal (Clear)

Cystinuria, Type B, Variant 2

WT/WT

Normal (Clear)

Cystinuria, Type B, Variant 3

WT/WT

Normal (Clear)

Cystinuria, Type B, Variant 4

WT/WT

Normal (Clear)

Cystinuria, Type B, Variant 5

WT/WT

Normal (Clear)

Dihydropyrimidinase Deficiency

WT/WT

Normal (Clear)

Epidermolysis Bullosa Simplex

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)

Feline Niemann-Pick Disease

WT/WT

Normal (Clear)

Feline Spongy Encephalopathy

WT/WT

Normal (Clear)

Forebrain Commissural Malformation

WT/WT

Normal (Clear)

Gangliosidosis GM2A

WT/WT

Normal (Clear)

Glycogen Storage Disease, Type IV

WT/WT

Normal (Clear)

GM1 Gangliosidosis

WT/WT

Normal (Clear)

GM2 Gangliosidosis, Type II (Burmese Type)

WT/WT

Normal (Clear)

GM2 Gangliosidosis, Type II

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)

Hemophilia B, Variant 1

WT/WT

X-Linked Female Normal

Hemophilia B, Variant 2

WT/WT

X-Linked Female Normal

Hyperlipoproteinemia

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)

Hypogonadotropic Hypogonadism

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

L-2-Hydroxyglutaric Aciduria

WT/WT

Normal (Clear)

Methemoglobinemia, Variant 1

WT/WT

Normal (Clear)

Methemoglobinemia, Variant 2

WT/WT

Normal (Clear)

Mucolipidosis II

WT/WT

Normal (Clear)

Mucopolysaccharidosis Type I

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)

Multiple Drug Resistance

WT/WT

Normal (Clear)

Myotonia Congenita

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)

Niemann-Pick C2 Disease

WT/WT

Normal (Clear)

Oculocutaneous Albinism

WT/WT

Normal (Clear)

Polycystic Kidney Disease

WT/WT

Normal (Clear)

Polycystic Kidney Disease (Siberian Type)

WT/WT

Normal (Clear)

Primary Congenital Glaucoma

WT/WT

Normal (Clear)

Primary Hyperoxaluria Type II

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)

Pyruvate Kinase Deficiency

WT/WT

Normal (Clear)

Rod-Cone Dysplasia

WT/WT

Normal (Clear)

Spinal Muscular Atrophy

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)


F5 Purfectpawzcats Kenya of CarolinaSavannah

F5 Purfectpawzcats Zetia of CarolinaSavannah