GGP Bovine 100K
SKU No. 40 | Catalog No.
Recently upgraded to include 100,000 markers, Neogen’s GGP Bovine 100K is the backbone of many formal genetic evaluations. Key features of the GGP Bovine 100K include:
- Smart design. SNPs specifically chosen for high minor allele frequency and uniform coverage of the genome for most beef and dairy breeds of cattle.
- Comprehensive information. Includes significant overlap to many other bovine SNP panels for increased imputation accuracy.
- Parentage Verification. Includes all commonly utilized USDA and ISAG parentage markers.
$43.00 each
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Minimum quantity required: 1
This item must be ordered in multiples of one case. Quantity per case: 1
Additional Testing
Additional testing is available to add in the next step when uploading your submission form.
Congenital Myasthenic Syndrome (CMS)
A genetic condition that is associated with progressive skeletal muscle weakness and calf mortality
Deficiency of Uridine Monophosphate Synthase (DUMPS)
Characterized by lowered blood activity of enzyme uridine monophosphate synthase (UMPS), DUMPS leads to embryonic death in early stage of pregnancy.
Bovine Lueukocyte Adhesion Deficiency (BLAD)
Delayed wound healing and stunt growth
Brachyspina
Genetic disorder associated with still born calves, vertebrae malformation, reduced body weight, shorten spine and long legs, abnormal formation of kidney, testicles and heart.
Red Charlie (RC)
Homozygous black animals which carry Red Charlie should be treated as carriers for the red coat color gene.
Learn MoreCoat Color Dilutor (DL)
This dilution gene causes black coat color to be gray and red coat color to be yellow.
Learn MoreDigital Subluxation (DS)
Affected animals are known to have malformation of the rear pastern or pasterns.
Learn MoreDun Coat Color (DN)
This dilution gene causes black coat color to be diluted to shades of dark brown to golden. Red pigment is not diluted by this mutation.
Learn MoreKappa Casein
A genetic test that can help characterize a key protein in cheese making what influences the renneting time and curd firmness
Leptin
By regulating appetite and energy use, leptin can have an influence on many aspects of dairy and beef production. Classifying the type of leptin gene in beef.
Tenderness
A genetic test that is associated with meat that requires less shear force to cut (tenderness)
Holstein Cholesterol Deficiency
BreedSeek
BreedSeek delivers primary and secondary majority breeds and percentages for the following breeds: Akaushi, Angus, Brahman, Gelbvieh, Hereford, Holstein, Jersey, Limousin, Nelore, Red Angus, Simental, Shorthorn, and Wagyu.
Stearoyl CoA Desaturase (SCD)
Cattle may have a genetic variant that produces a superior fat composition (lower melting point).
Protoporphyria
Calves affected by Protoporphyria have an acute form of photosensitization resulting in hair loss and/or the formation of ulcers on areas exposed to sunlight. In some instances this condition is lethal.
Learn MoreA2 Milk
A2 Beta casein – A2 beta casein protein that is less common than the A1 beta casein protein typically found in milk. Some studies have demonstrated human health benefits associated with A2 milk.
Beta Lactoblobulin
β-Lactoglobulin is the major whey protein found in milk. Several genetic variants have been identified, the main ones in the cow being labelled A and B. Certain variation may be of advantage in the fo
Pompes (E7, E13, E18)
A genetic condition that is often affilated with glycogen buildup that interfers with normal tissue function
Maple Syrup Urine Disease (MSUD)
Causes mental and physical retardation, feeding problems, and a maple syrup odor to the urine.
Learn MoreFish Milk
Metabolism error associated with a fishy off-flavor in cow’s millk due to elevated levels of trimethylamine
Learn MoreTibial Hemimelia (TH)
Affected animals are born with severe deformities including twisted rear legs with fused joints, large abdominal hernias and/or skull deformities.
Learn MoreOculocutaneous Hypopigmentation (OH)
Affected animals are known to have eyes with irises that are pale blue around the pupil.
Learn MoreNeuropathic Hydrocephalus (NH)
More commonly known as "waterhead", affected animals are born dead with an extremely large head with little or no brain material or spinal cord.
Learn MoreOsteopetrosis (OS)
Also known as “marble bone”, affected animals phenotypically possess a short lower jaw and impacted molars as well as elongated, fragile bones that are easily broken.
Learn MorePulmonary Hypoplasia Anasarca (PHA)
Affected animals are stillborn due to underdeveloped lungs and swelling caused by excessive fluid retention.
Learn MoreMyostatin (MYO)
Most commonly referred to as “double muscling”. Possible variants tested include C313Y, nt419, E226X, nt821, E291X, Q204X, D182N, F94L, and S105C.
Learn MoreAlpha Mannosidosis (MA)
Affected animals develop poor coordination and an aggressive disposition when disturbed.
Learn MoreSeekSire™ Parentage
SeekSire™ parentage testing compares DNA markers from bulls (or cows) with DNA from calves to verify the calves’ parentage.
Learn MoreHorned/Polled (HP)
Genomic test to determine an animal's carrier status for the horned gene.
Learn MoreHypotrichosis (HY)
Also known as "hairlessness", affected animals have partial or total hair loss.
Learn MoreIdiopathic Epilepsy (IE)
Also referred to as “shaker calf”, affected animals are prone to seizures.
Learn MoreDevelopmental Duplication (DD)
Affected animals are born with all, or part of, an extra limb.
Learn MoreChondrodysplasia (CHO)
"Bulldog" calves, the lethal form, are stillborn. Dwarfism of the Dexter breed resulting in shortened legs.
Learn MoreComplex Vertebral Malformation (CVM)
Complex Vertebral Malformation (CVM) is a lethal hereditary syndrome in Holstein animals causing malformed calves that are aborted or die shortly after birth.
Learn MoreContractural Arachnodactyly (CA)
Also known as “fawn calf”, CA results in an abnormality of skeletal development in Angus cattle.
Learn MoreArthrogryposis Multiplex (AM)
Known as "curly calf", affected animals (those with two copies of the recessive allele) are stillborn and have a twisted or curved spine and extended and contracted limbs.
Learn MoreIgenity® Beef
The first and only genomic profile designed for crossbred commercial cattle, Igenity® Beef utilizes DNA to predict genetic merit in both heifers and steers.
Learn MoreIgenity® Select
Igenity Select is a comprehensive, full-power selection tool that allows you to make rapid genetic progress in your herd.
Learn MoreBovine Viral Diarrhea Virus - Persistently Infected (BVDV-PI)
Neogen® offers fast and accurate testing for the detection of Bovine Viral Diarrhea Virus (BVDV).
Igenity® BCHF
Igenity® BCHF is a genomic test that estimates an animal’s genetic risk for heart failure. By DNA testing cattle for BCHF, producers can confidently identify animals with the genetics to improve bovine heart health.
Learn MoreBand3 Spheocytosis
The absence of Band3 results in hereditary spherocytosis in Japanese black cattle.
Chediak-Higashi Syndrome (CHS)
Cattle with this syndrome often have an unusually pale coat color.
F11 Japanese Cattle Add-on
Factor 11 (Factor XI) Deficiency results in longer coagulation time for blood after injury or an umbilical cord that won't cease bleeding for Red and Black Wagyu cattle.
BPA
Bovine Progressive Ataxia results in the onset of unsteady gait and stiff hind limbs in Charolais cattle.
GWB
GWB provides status for Band3, F11, CHS, and IARS for Japanese cattle.
IARS
Isoleucyl-tRNA synthetase Disorder results in low birthweight, weakness, and poor suckling in Wagyu cattle.
RP1 Retinal Degeneration
Retinal Degeneration results in progressive death of photoreceptor cells.
| Specifications | ||
|---|---|---|
| Brand | GeneSeek® Genomic Profiler™ | |
| Breeds Supported | All breeds supported | |
| Species | Bovine, Beef, Dairy | |
| Data Results | GGP Bovine 100K provides raw genotype information back to industry partners for use in a formal genetic evaluation. Parentage analysis can be performed by Neogen, if desired. | |
| Submission Information | Producers may purchase GGP Bovine 100K through one of Neogen’s partner breed associations or their genetic evaluation provider. If interested in the product for research purposes, please contact Neogen directly. | |
| Genetic Conditions | BVDV, Chondrodysplasia (CHO) , Coat Color, Complex Vertebral Malformation (CVM), Developmental Duplication (DD), Dun Coat Color (DN), Horned/Polled (HP), Hypotrichosis (HY), Idiopathic Epilepsy (IE), Alpha Mannosidosis (MA) , Maple Syrup Urine Disease (MSUD), Myostatin (MYO), Neuropathic Hydrocephalus (NH), Osteopetrosis (OS), Pulmonary Hypoplasia Anasarca (PHA), BLAD, DUMPS, Brachyspina, Kappa Casein, Leptin, Tenderness, A2 Milk, CMS, Fish Milk | |
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