Laladoodles Altair
Meet our Up and coming mini stud! Our handsome laladoodles Altair lives with us inside our home and is the sweetest boy and the best house dog! He is so smart he learned to touch the fluent pet buttons as a puppy! He is friendly with other dogs and also to people he meets ! He enjoys being my companion on walks to pick up coffee at Columbia city! He is such a sweet dog that loves to play fetch with our other dogs. He is truly my dream dog! We are so blessed to have him in our life! A perfect size and temperament for our household. Altair has a fleecey wavy coat that is a beautiful dark red color with white markings!
Altair will be having a full panel genetics testing, Eye CerF , and Pennhipp testing .
Please reach out to me if you would be interested in using Altair’s stud service in the future . Thank you!
20 lbs
Video of Altair https://m.youtube.com/watch?v=B0HTBDdYnUQ
Genetic Diseases Orivet Test Results 07/2025
Achromatopsia (Labrador Type)
NORMAL (N/N) – [NO VARIANT DETECTED]
Single ReportAutosomal Hereditary Recessive Nephropathy
NORMAL (N/N) – [NO VARIANT DETECTED]
Single ReportCentronuclear Myopathy (Labrador Retriever Type)
NORMAL (N/N) – [NO VARIANT DETECTED]
Single ReportChondrodystrophy (CDDY) & Intervertebral Disc Disease (IVDD) [RESEARCH ONLY]
NORMAL (N/N) FOR CFA18 (SHORT LIMB) & CARRIER (P/N) FOR CFA12 (IVDD)
Single ReportCone-Rod Dystrophy I – PRA (crd -4/cord I)
NORMAL (N/N) – [NO VARIANT DETECTED]
Single ReportCongenital Methemoglobinemia (Poodle and Pomeranian Type)
NORMAL (N/N) – [NO VARIANT DETECTED]
Single ReportCongenital Myasthenic Syndrome (Labrador Retriever Type)
NORMAL (N/N) – [NO VARIANT DETECTED]
Single ReportCopper Toxicosis (ATP7B & ATP7A) (Labrador Retriever Type)
N) FOR ATP7B
Single ReportDegenerative Myelopathy
NORMAL (N/N) – [NO VARIANT DETECTED]
Single ReportDyserythropoietic Anemia and Polymyopathy (DAMS) (Labrador Retriever)
NORMAL (N/N) – [NO VARIANT DETECTED]
Single ReportEhlers-Danlos Syndrome (Labrador Retriever Type), Variant 2
NORMAL (N/N) – [NO VARIANT DETECTED]
Single ReportEhlers-Danlos Syndrome (Labrador Type)
NORMAL (N/N) – [NO VARIANT DETECTED]
Single ReportElliptocytosis B-spectrin (Labrador Retriever/Poodle Type)
NORMAL (N/N) – [NO VARIANT DETECTED]
Single ReportExercise Induced Collapse (Retriever Type)
NORMAL (N/N) – [NO VARIANT DETECTED]
Single ReportGangliosidosis GM2 (Poodle Type)
NORMAL (N/N) – [NO VARIANT DETECTED]
Single ReportGeneralised PRA 1 (Golden Retriever Type)
NORMAL (N/N) – [NO VARIANT DETECTED]
Single ReportGloboid Cell Leukodystrophy/Krabbe’s Disease
NORMAL (N/N) – [NO VARIANT DETECTED]
Single ReportHereditary Nasal Parakeratosis/Dry Nose (Labrador Retriever Type)
NORMAL (N/N) – [NO VARIANT DETECTED]
Single ReportHyperuricosuria
NORMAL (N/N) – [NO VARIANT DETECTED]
Single ReportIvermectin Sensitivity MDR1 (Multi Drug Resistance)
NORMAL (N/N) – [NO VARIANT DETECTED]
Single ReportMalignant Hyperthermia
NORMAL (N/N) – [NO VARIANT DETECTED]
Single ReportMyotonia Congenita (Labrador Retriever Type)
NORMAL (N/N) – [NO VARIANT DETECTED]
Single ReportMyotubular Myopathy X-Linked (Labrador Retriever Type)
NORMAL (N/N) – [NO VARIANT DETECTED]
Single ReportNarcolepsy (Labrador)
NORMAL (N/N) – [NO VARIANT DETECTED]
Single ReportNeonatal Encephalopathy (Poodle Type)
NORMAL (N/N) – [NO VARIANT DETECTED]
Single ReportOsteochondrodysplasia (Min Poodle Type)
NORMAL (N/N) – [NO VARIANT DETECTED]
Single ReportPhosphofructokinase Deficiency (Spaniel Type)
NORMAL (N/N) – [NO VARIANT DETECTED]
Single ReportProgressive Rod Cone Degeneration (prcd) – PRA
NORMAL (N/N) – [NO VARIANT DETECTED]
Single ReportPyruvate Kinase Deficiency (Labrador Type)
NORMAL (N/N) – [NO VARIANT DETECTED]
Single ReportRetinal Dysplasia/Oculoskeletal Dysplasia 1
NORMAL (N/N) – [NO VARIANT DETECTED]
Single ReportSkeletal Dysplasia 2 (Mild Disproportionate Dwarfism)
NORMAL (N/N) – [NO VARIANT DETECTED]
Single ReportStargardt Disease (Retinal Degeneration)
NORMAL (N/N) – [NO VARIANT DETECTED]
Single Reportvon Willebrand’s Disease Type I
NORMAL (N/N) – [NO VARIANT DETECTED]
Single Report
Genetic Traits Test Results Orivet 07/2025
| A Locus (Agouti) | at/at – TAN POINTS/BLACK & TAN or TRICOLOUR MAY BE BRINDLED [SEE K LOCUS] | Single Report | |
| Brown TYRP1 [Lancashire Heeler Type] = Bl | BL/BL – DOES NOT CARRY BROWN/LIVER [TYRP1] | Single Report | |
| Curly Coat/Hair Curl (KRT71 R151W) | ONE COPY OF THE R151W (CU/Cu) VARIANT DETECTED – MOST LIKELY TO HAVE MODERATE ‘WAVY’ CURLY COAT PHENOTYPE | Single Report | |
| D (Dilute) Locus | D/D – NO COPY OF MLPH-D ALLELE (DILUTE) – PIGMENT IS NORMAL | Single Report | |
| E Locus – (Cream/Red/Yellow) | e/e – HOMOZYGOUS FOR NON-EXTENSION [WHITE/YELLOW/APRICOT/WHEATEN] | Single Report | |
| EM (MC1R) Locus – Melanistic Mask | En/En – NO MELANISTIC MASK (En) EXTENSION ALLELE | Single Report | |
| Improper Coat/Furnishings (RSPO2) | F/F – POSITIVE FOR IMPROPER COAT/FURNISHINGS (OPEN FACE) – WILL SHOW FURNISHINGS | Single Report | |
| K Locus (Dominant Black) | K/K – DOMINANT BLACK – SOLID [WILL NOT BE BRINDLED or EXPRESS AGOUTI] | Single Report | |
| Long Hair Gene (Canine C95F) | POSITIVE – SHOWING THE PHENOTYPE | Single Report | |
| M Locus (Merle/Dapple) | m [171bp] / m [171bp] – NON MERLE SOLID COAT (NO CHANGE TO COAT or EYE COLOUR) | Single Report | |
| Pheomelanin Intensity CFA18 (Poodle/Coonhound Type) | I/i- ONE COPY OF THE CFA18 INTENSITY ALLELE (NOT LIKELY TO SHOW EXTREME DILUTION) | Single Report | |
| Pheomelanin Colour Intensity CFA2 (Various Breeds) | I/i- ONE COPY OF THE CFA2 INTENSITY ALLELE (NOT LIKELY TO SHOW EXTREME DILUTION) | Single Report | |
| Pheomelanin Colour Intensity CFA21 (Various Breeds) | i/i- TWO COPIES OF THE CFA21 INTENSITY ALLELE (LIKELY TO SHOW EXTREME DILUTION) | Single Report | |
| Pheomelanin Intensity CFA15 (Retriever and Poodle Type) | i/i- TWO COPIES OF THE CFA15 INTENSITY ALLELE (LIKELY TO SHOW EXTREME DILUTION) | Single Report | |
| Pied (BOTH SINE and REPEAT VARIANTS) | S/sp – CARRIER OF PIEBALD [LIMITED WHITE SPOTTING, FLASH OR PARTI] | Single Report | |
| Shedding (MC5R) | SHD/SHD [LOW SHEDDING] – NO COPIES OF THE SHEDDING (MC5R) VARIANT DETECTED [REFER TO R151W (IC) FOR LEVEL] | Single Report | |
| Ticking & Roan (TR) | r/r – NO ROAN or TICKING IN COAT | Single Report | |
| – | Brown Deletion = Bd | Bd/Bd – DOES NOT CARRY BROWN/RED/LIVER or CHOCOLATE [DELETION] | Single Report |
| – | Brown Insertion = Bc | Bc/Bc – DOES NOT CARRY BROWN/RED/LIVER or CHOCOLATE [INSERTION] | Single Report |
| – | Brown Stop Codon = Bs | Bs/Bs – DOES NOT CARRY BROWN/RED/LIVER or CHOCOLATE [STOP CODON] | Single Report |
| – | Coat Composition CFA28 Gene (Double/Single Coat) | UDC/UDC – NO COPY OF THE DOUBLE COAT (DENSE UNDERCOAT) PHENOTYPE DETECTED | Single Report |
