Bovine (Beef) Genomic Panels

Partner With Us.

Our team of tech experts and scientist at Agritech Genetics can develop breed specific panels for agricultural organizations.  We provide quick turnaround time for all our animal genomic products and services.

 

  • STR/Microsatellite Genotyping

  • SNP Genotyping

  • NGS Sequencing

  • Custom Analysis

  • Evaluation Tools

  • Custom Genomic Panels

  • Disease Screening

  • Production Trait Analysis

  • Parentage Verification

Custom Genetic Panels

Custom panels can be designed in as little as 1 to 3 months. For details about your genetic service, please contact us by email or speak with a genomic specialist at 385-282-6335

Breed Specific Panels

Agritech Genetics has developed the most advanced breed specific 

Agritech Genetics Comprehensive Beef Panel

Genomic Evaluation Traits

  • Tenderness 

  • Marbling

  • Fertility

  • Body Composition

  • Growth

  • Meat Quality

  • Consumer Health Traits

  • AND MORE

Coat Color

  • Homozygous Black / Red

  • Belgian Blue Cool Gray

  • Charolais Dilution

  • Dexter Brown

  • Red Angus

  • Silver Dilution

  • Roan

  • AND MORE

Horned / Polled

  • Horned / Polled

Parentage Verification

*** When requesting parentage test, verify that all possible parents have been genotyped by Agritech Genetics prior to sample submission. If parents have not been genotyped, please include parent samples when placing an order. Include all information on the sample submission form.

Genetic Diseases and Abnormalities (Beef Cattle)

  • Abortion (Emryonic Lethality) - Beef Breeds

  • Achondrogenesis, type II

  • Albinism

  • Alpha Mannosidosis

  • Anhidrotic ectodermal dysplasia

  • Anhidrotic ectodermal dysplasia, EDAR-related

  • Arachnomelia, BTA23

  • Arthrogryposis

  • Arthrogryposis Multiplex (AM)

  • Arthrogryposis, lethal syndrome

  • Axonopathy

  • Beta Mannosidosis

  • Bovine Arachnomelia Syndrome

  • Bovine Leukocyte Adhesion Deficiency (BLAD)

  • Bovine Spongiform Encephalopathy (BSE)

  • Briskets Disease (High Altitude Sickenss)

  • Caprine-like Generalized Hypoplasia Syndrome

  • Cardiomyopathy and woolly haircoat syndrome

  • Chediak-Higashi syndrome

  • Cholesterol Deficiency (CD)

  • Chondrodysplasia (2 Mutations)

  • Citrullinemia

  • Claudin 16 Deficiency  

  • Coat colour, albinism

  • Coat colour, albinism, oculocutaneous type IV

  • Congenital Muscular Dystonia I

  • Congenital Muscular Dystonia II

  • Congenital Myoclonus

  • Contractual Arachnodactyly (CA)

  • Crooked Tail Syndrome

  • Deficiency of uridine monophosphate synthase

  • Developmental Duplication (DD)

  • Dwarfism, Angus

  • Dwarfism, Fleckvieh

  • Dystrophic Epidermolysis Bullosa

  • Ehlers-Danlos syndrome, type VII (Dermatosparaxis)

  • Epidermolysis bullosa, dystrophic

  • Epidermolysis bullosa, junctionalis, LAMA3-related

  • Factor XI deficiency

  • Fanconi syndrome

  • Fleckvieh Haplotype 4 (FH4)

  • Forelimb-girdle muscular anomaly

  • Freemartin

  • German White Fleckvieh Syndrome

  • Glycogen storage disease II

  • Glycogen storage disease V

  • Goitre, familial

  • Haemophilia A

  • Hydrallantois

  • Hypotrichosis

  • Hypotrichosis, KRT71-related

  • Hypotrichosis, streaked

  • Ichthyosis congenita

  • Male subfertility

  • Maple syrup urine disease

  • Maple Syrup Urine Disease

  • Marfan syndrome

  • Mucopolysaccharidosis IIIB

  • Mulefoot

  • Multiple ocular defects

  • Muscular hypertrophy (double muscling)

  • Myasthenic syndrome, congenital, CHRNE-related

  • Myostatin

  • Neurocristopathy

  • Neuronal ceroid lipofuscinosis, 5

  • Neuropathic Hydrocephalus (NH)

  • Oculocutaneous Hypopigmentation (OH)

  • Osteogenesis imperfecta, type II, COL1A1-related

  • Osteopetrosis (OS)

  • Osteopetrosis with gingival hamartomas

  • Paunch Calf Syndrome

  • Perinatal weak calf syndrome

  • Protoporphyria

  • Rat Tailed

  • Retinitis pigmentosa 1

  • RNF11

  • Scurs, type 2

  • Slick hair

  • Sperm, short tail

  • Spherocytosis

  • Spinal Muscular Atrophy

  • Spongiform encephalopathy (mad cow disease)

  • Thrombopathia

  • Tibial Hemimelia

  • Weaver syndrome

  • Xanthinuria, type II

  • Zinc deficiency-like syndrome