GENETIC ANALYSIS REPORT

OWNER'S DETAILS

Laurence Delaloye

L'lle D'oriane Laragne, 05300

ANIMAL'S DETAILS

RegisteredName: AlfapointIvan Pet Name: Ivan
Breed: British Shorthair

COLLECTION DETAILS

Case Number: 15-063250 Collected By: Dr. R Rabuel

RegistrationNo: Microchip No: Sex:

Date of Test: Approved Coll. Mthd.:

Pending 972270000305995 Male

17/01/15 Yes

Sample with Lab ID Number 15-063250 was received at Orivet Genetics, DNA was extracted and analysed with the following results reported:

DISEASE(S):

PYRUVATE KINASE (PK) DEFICIENCY (NORMAL / CLEAR - NO MUTATION DETECTED) MUCOPOLYSACCHARADOSIS (NORMAL / CLEAR - NO MUTATION DETECTED)
POLYCYSTIC KIDNEY DISEASE (NORMAL / CLEAR - NO MUTATION DETECTED)
NEIMANN-PICK DISEASE TYPE C (NORMAL / CLEAR - NO MUTATION DETECTED)
FAMILIAL EPISODIC HYPOKALEAMIC POLYMYOPATHY (NORMAL / CLEAR - NO MUTATION DETECTED) HYPERTROPHIC CARDIOMYOPATHY - MAINE COON (NORMAL / CLEAR - NO MUTATION DETECTED) HYPERTROPHIC CARDIOMYOPATHY - RAGDOLL (NORMAL / CLEAR - NO MUTATION DETECTED) PROGRESSIVE RETINAL ATROPHY (PRA) CEP 290 (PRA-RDC) (NORMAL / CLEAR - NO MUTATION DETECTED) PROGRESSIVE RETINAL ATROPHY (PRA) CRX (PRA-RDY) (NORMAL / CLEAR - NO MUTATION DETECTED) SPINAL MUSCULAR ATROPHY (SMA) - MAINE COON (NORMAL / CLEAR - NO MUTATION DETECTED) GLYCOGEN STORAGE DISEASE TYPE IV (NORMAL / CLEAR - NO MUTATION DETECTED)

GANGLIOSIDOSI- GM2 (NORMAL / CLEAR - NO MUTATION DETECTED)

ALBINISM (ALB N / ALB N - NO ALBINO MUTATION DETECTED)
AMBER (E/E - NO COPIES OF AMBER MUTATION DETECTED)
DILUTION (d/d TWO COPIES OF DILUTE ALLELE - COAT COLOR IS DILUTED) BLOOD GROUP (N/b = TYPE A/b or AB/b (b/non-b) CARRIER of TYPE B)

CHOCOLATE AND CINAMMON (bc/bc)

COLOURPOINT RESTRICTION (cs/cs - SIAMESE)
AGOUTI (a/a NON AGOUTI - IF BRED TO A NON-AGOUTI ONLY NON-AGOUTI)
LONG HAIR SHORTHAIR (N/N = NONE OF THE 4 LONG HAIR MUTATIONS DETECTED)

WHITE GLOVES (Ng/Ng - NO GLOVE MUTATION DETECTED)

TRAIT(S):

RESULTS REVIEWED AND CONFIRMED BY:

Dr. Noam Pik BVs MDSV George Sofronidis BSc (Hons) 

GENETIC ANALYSIS REPORT

OWNER'S DETAILS

Laurence Delaloye

L'lle D'oriane Laragne, 05300

ANIMAL'S DETAILS

Registered Name: Biyanka British Flowering Pet Name: Biyanka
Breed: British Shorthair

COLLECTION DETAILS

Case Number: 15-063220 Collected By: Dr. R Rabuel

Registration No: Microchip No: Sex:

Date of Test: Approved Coll. Mthd.:

Pending 643094100333657 Female

17/01/15 Yes

Sample with Lab ID Number 15-063220 was received at Orivet Genetics, DNA was extracted and analysed with the following results reported:

DISEASE(S):

PYRUVATE KINASE (PK) DEFICIENCY (NORMAL / CLEAR - NO MUTATION DETECTED) MUCOPOLYSACCHARADOSIS (NORMAL / CLEAR - NO MUTATION DETECTED)
POLYCYSTIC KIDNEY DISEASE (NORMAL / CLEAR - NO MUTATION DETECTED)
NEIMANN-PICK DISEASE TYPE C (NORMAL / CLEAR - NO MUTATION DETECTED)
FAMILIAL EPISODIC HYPOKALEAMIC POLYMYOPATHY (NORMAL / CLEAR - NO MUTATION DETECTED) HYPERTROPHIC CARDIOMYOPATHY - MAINE COON (NORMAL / CLEAR - NO MUTATION DETECTED) HYPERTROPHIC CARDIOMYOPATHY - RAGDOLL (NORMAL / CLEAR - NO MUTATION DETECTED) PROGRESSIVE RETINAL ATROPHY (PRA) CEP 290 (PRA-RDC) (NORMAL / CLEAR - NO MUTATION DETECTED) PROGRESSIVE RETINAL ATROPHY (PRA) CRX (PRA-RDY) (NORMAL / CLEAR - NO MUTATION DETECTED) SPINAL MUSCULAR ATROPHY (SMA) - MAINE COON (NORMAL / CLEAR - NO MUTATION DETECTED) GLYCOGEN STORAGE DISEASE TYPE IV (NORMAL / CLEAR - NO MUTATION DETECTED)

GANGLIOSIDOSI- GM2 (NORMAL / CLEAR - NO MUTATION DETECTED)

ALBINISM (ALB N / ALB N - NO ALBINO MUTATION DETECTED)
AMBER (E/E - NO COPIES OF AMBER MUTATION DETECTED)
DILUTION (d/d TWO COPIES OF DILUTE ALLELE - COAT COLOR IS DILUTED) BLOOD GROUP (TYPE Aor AB (b/non-b) CARRIER of B)

CHOCOLATE AND CINAMMON (bc/bc)

COLOURPOINT RESTRICTION (cs/cs - SIAMESE)
AGOUTI (a/a NON AGOUTI - IF BRED TO A NON-AGOUTI ONLY NON-AGOUTI)
LONG HAIR SHORTHAIR (N/M4 = ONE COPY (CARRIER) OF THE LHG MUTATION DETECTED)

WHITE GLOVES (Ng/Ng - NO GLOVE MUTATION DETECTED)

TRAIT(S):

RESULTS REVIEWED AND CONFIRMED BY:

Dr. Noam Pik BVs MDSV George Sofronidis BSc (Hons)