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.

Pandora'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 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)


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

Kenya is renound for her beautiful green eyes and black nose.  She is extremely vocal and she loves attention.  She is the full sister of Zetia.  She and Zetia famously coparented the 10 Pack litter.

Kenya's Disease Testing Results

Demographic Information

Call Name Kenya

Registered Name Purfectpawzcats Kenya

CarolinaSavan

Breed Savannah

Sex Female

Owner michael ayers

DOB Aug. 20, 2021

Registration # SBT 082021 119

Tattoo -

Microchip -

Laboratory # 386274

Report Date March 6, 2023

These tests were developed and performed by Paw Print Genetics®, Spokane WA.

Explanation of Results

Normal A 'Normal' result means that your cat does not have the mutation that causes the associated

genetic disease.

Carrier A 'Carrier' result indicates that your cat has inherited one copy of the mutation that has been

reported to cause this genetic disease. Your cat may not be clinically affected by this mutation

because two copies of the mutation are usually required to cause disease.

Carrier / At–Risk A 'Carrier / At–Risk' result indicates that your cat inherited one copy of the mutation that has

been reported to cause this genetic disease. Based on the mode of genetic inheritance for this

particular disease, inheriting one mutant copy of the gene may result in the disease. Cats with

one copy of the mutation may have a milder phenotype as compared to cats with two copies of

this mutation.

At–Risk / Affected An 'At–Risk / Affected' result indicates that your cat inherited one or two copies of the

mutation that has been reported to cause this genetic disease. Based on the mode of genetic

inheritance for this particular disease, inheriting one or two mutant copies of the gene may

result in the disease.

Page 1 of 7

No Result 'No Result' indicates that we were unable to obtain a genotype for your cat for this specific

disease or trait and does not mean that your cat is a carrier or at-risk for this disease. There are

a variety of reasons why a specific test may not provide a reportable result. Unique variations in

the genetic code of some individuals may exist and cause certain regions of the genome to not

perform properly with a specific test. In addition, suboptimal sampling of the cat’s cheek cells

could also result in poor sample performance due to inadequate cell counts, bacterial and fungal

growth, or the presence of other test inhibitors. An acceptable level of tests with no results has

been determined by Paw Print Genetics. Cats with at least 90% of the test results are

determined to be acceptable and reportable. If your cat has an unacceptable level of tests with

no results, you will be contacted for a new sample to repeat the testing.

Please review our testing terms and disclaimers regarding your results.

WT: wild type (normal) M: mutant Y: Y chromosome (male)

Breed Profile

Disease Name Genotype Interpretation

Pyruvate Kinase Deficiency WT/WT Normal (clear)

WT: wild type (normal) M: mutant Y: Y chromosome (male)

Coat Colors & Traits

Trait Name Genotype Interpretation

ABC Blood Group System A/A A blood group

ABC Locus - B Group Variant 1 - b1 0

ABC Locus - B Group Variant 2 - b2 0

ABC Locus - C Group Variant - ac 0

Agouti Coat Color - A Locus A/A Tabby expression allowed

Amber and Russet Coat Color - E Locus E/E Non-amber, darkly

pigmented coat color

E Locus - Amber Variant - e 0

E Locus - Russet Variant - er 0

Brown Coat Color - B Locus B/b1 Black coat color (cinnamon,

red carrier)

Page 2 of 7

B Locus - Cinnamon Variant - b1 1

B Locus - Chocolate Variant - b 0

Coat Type - Curly (Devon Rex, Selkirk Rex Type) or Hairless

(Sphynx Type) - R Locus

R/R Straight coat

R Locus - Selkirk Rex Curly Variant - SR 0

R Locus - Devon Rex Curly Variant - re 0

R Locus - Sphynx Hairless Variant - hr 0

Curly Coat (Cornish Rex Type) Cu/Cu Straight coat

Dilute Coat Color - D Locus D/D Non-dilute