Cooper's Elijah Chariot of Fire - "'Lijah"
Registered with Orthopedic Foundation for Animals (OFA) and Companion Animal Eye Registry (CAER) at age 4 (6/17).
Elbows good
Hips normal
Eyes normal, free of disease
Registered with Orthopedic Foundation for Animals (OFA) and Companion Animal Eye Registry (CAER) at age 4 (6/17).
Elbows good
Hips normal
Eyes normal, free of disease
Cooper's Opal Spirit of Elizabeth - "Opal"
Registered with Orthopedic Foundation for Animals (OFA) and Companion Animal Eye Registry (CAER) at age 3 (6/17).
Elbows normal
Hips excellent
Eyes normal, free of disease
Registered with Orthopedic Foundation for Animals (OFA) and Companion Animal Eye Registry (CAER) at age 3 (6/17).
Elbows normal
Hips excellent
Eyes normal, free of disease
PBAS Primero De Mayo - "Maya"
Registration with Orthopedic Foundation for Animals (OFA) and Companion Animal Eye Registry pending.
Canine Genetic Health Certificate™
Call Name: Maya Registered Name: PBAS Primero De Maya Breed: Australian Shepherd Sex: Female DOB: March 12, 2018
Laboratory #: 118961 Registration #: Certificate Date: Feb. 18, 2019
This canine's DNA showed the following genotype(s): Disease Gene Genotype Interpretation Collie Eye Anomaly NHEJ1 WT/WT Normal (clear) Cone Degeneration CNGB3 WT/WT Normal (clear) Degenerative Myelopathy SOD1 WT/WT Normal (clear) Hereditary Cataracts (Australian Shepherd Type) HSF4 WT/WT Normal (clear) Hyperuricosuria SLC2A9 WT/WT Normal (clear) Intestinal Cobalamin Malabsorption (Australian Shepherd Type) AMN WT/WT Normal (clear) Multidrug Resistance 1 ABCB1 WT/M Carrier (At-Risk) Multifocal Retinopathy 1 BEST1 WT/WT Normal (clear) Neuronal Ceroid Lipofuscinosis 6 CLN6 WT/WT Normal (clear) Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration PRCD WT/WT Normal (clear) WT, wild type (normal); M, mutant; Y, Y chromosome (male)
Registration with Orthopedic Foundation for Animals (OFA) and Companion Animal Eye Registry pending.
Canine Genetic Health Certificate™
Call Name: Maya Registered Name: PBAS Primero De Maya Breed: Australian Shepherd Sex: Female DOB: March 12, 2018
Laboratory #: 118961 Registration #: Certificate Date: Feb. 18, 2019
This canine's DNA showed the following genotype(s): Disease Gene Genotype Interpretation Collie Eye Anomaly NHEJ1 WT/WT Normal (clear) Cone Degeneration CNGB3 WT/WT Normal (clear) Degenerative Myelopathy SOD1 WT/WT Normal (clear) Hereditary Cataracts (Australian Shepherd Type) HSF4 WT/WT Normal (clear) Hyperuricosuria SLC2A9 WT/WT Normal (clear) Intestinal Cobalamin Malabsorption (Australian Shepherd Type) AMN WT/WT Normal (clear) Multidrug Resistance 1 ABCB1 WT/M Carrier (At-Risk) Multifocal Retinopathy 1 BEST1 WT/WT Normal (clear) Neuronal Ceroid Lipofuscinosis 6 CLN6 WT/WT Normal (clear) Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration PRCD WT/WT Normal (clear) WT, wild type (normal); M, mutant; Y, Y chromosome (male)
