MÂLES

SEVEN-TEEN A-IRBIS

Merci pour Elena (RUSSIA)

Sexe : Mâle

Race : British shorthair

Né le : 20/11/2017

Couler : seal silver shell point

Code : BRI-ns 1233

Test : PKD/FELV/FIV-négatif

Parents

Pére : RAM from ATIMTI

Mére : VALKIRIYA ATIMTI

Oscar La Ruche au Miel

Race : British Longhair

Couleur : chocolat golden shaded

Code couleur : BRL - by11

Sexe : Mâle

Date de naissance : 02.08.2018

 

Parents :

Père : Myosotis de la flamme douce

Mère : Magnolia de la flamme douce

Ned Star De La Flamme Douce (castré)

Couleur : chocolat golden shaded (bb)

Code couleur : by 11

Race : British Shorthair (BRI)

Date de naissance : 17/01/2017

Sexe : MÂLE

Test : PKD/FELV/FIV-Négatif

NEMO DE L’ILE D’ORIANE

Sexe : Mâle

Race : British shorthair

Né le : 23/05/2017

Couleur : fawn point et blanc

Cod :  BRI – p 3309

Parents

Pére : Alfapoint Ivan

Mére : Biyanka Britich Flowering

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) 

 

Nos chats sont testés :

 

PKD.FIV.FELV- négatifs

 

Identifiées Génétiquement