The Full Color/Pattern Panel combines both the coat color panel and the White Pattern Panel 2. This is the most comprehensive of the horse coat color/patterning panels offered by the Veterinary Genetics Laboratory (VGL).
 
TESTS INCLUDED IN THE PANEL:
Red Factor: The extension gene, or red factor, determines whether a horse will have a chestnut base coat color or a black or bay base coat color.
Agouti (Bay/Black): The agouti gene controls the distribution of black pigment, and determines whether a horse will have a bay or black base coat color.
Champagne: Champagne is a coat color dilution responsible for diluting both red and black pigment as well as causing pinkish/lavender skin and amber-colored eyes.
Cream: Cream is a dilution that causes the palomino, buckskin, smoky black, cremello, perlino, and smoky cream coat colors.
Dun Dilution: Dun is a coat color dilution characterized by lightening of the coat, with the head, lower legs, mane, and tail undiluted. Oftentimes, dun is also characterized by "primitive markings" such as a dark dorsal stripe, barring of the legs, shoulder stripes, and "cobwebbing" on the forehead.
Gray: The gray gene causes progressive depigmentation of the hair, often resulting in a color that is almost completely white by 6-8 years of age. The individual gray test will determine the number of copies of the gray allele (zygosity). The coat color panel tests detect presence or absence of the gray allele.
Pearl: Pearl is a coat color dilution that is characterized by a dilution of the coat, mane, and tail as well as a lightening of the skin.
Silver: The silver dilution dilutes black/brown pigment to lighten the manes and tails of black and bay horses to a flaxen or silver gray. The silver dilution is also associated with an inherited ocular syndrome known as Multiple Congenital Ocular Anomalies (MCOA).
Gray: The gray gene causes progressive depigmentation of the hair, often resulting in a color that is almost completely white by 6-8 years of age. The individual gray test will determine the number of copies of the gray allele (zygosity). The coat color panel tests detect presence or absence of the gray allele.
Tobiano: Tobiano is a white spotting pattern characterized by white on the body that crosses the topline.
Lethal White Overo (LWO): Lethal white overo (LWO) is a genetic disorder that results from two copies of the version of the gene causing the frame overo coat color pattern.
Sabino 1: Sabino is a white spotting pattern that is characterized by white markings on legs often accompanied by white ticking or roaning of the midsection and a blaze on the face.
Splashed White Mutations – SW1, SW2, SW3, SW4, SW5, and SW6: Splashed white is a variable white spotting pattern characterized by a broad blaze, extended white markings on the legs, variable white spotting on the belly, and often blue eyes. Six mutations in two different genes have been shown to cause the splashed white pattern.
Leopard Complex & Congenital Stationary Night Blindness: Leopard complex or appaloosa spotting is a white pattern in horses characterized by a variable amounts of white in the coat with or without pigmented leopard spots. Horses homozygous for this variant have an ocular condition known as congenital stationary night blindness.
Appaloosa Pattern-1 (PATN1): Appaloosa Pattern-1 is a modifier of the leopard complex spotting (LP) and controls the amount of white in the coat pattern.
Dominant White Mutations – W5, W10, W20, and W22: Dominant white is a variable white spotting pattern caused by many different mutations in the KIT gene. The VGL tests for the four most common mutations known as W5, W10, W20, and W22. Homozygosity for W5, W10, or W22 is thought to be non-viable.
 
Note: Does not include roan zygosity
Note: Gray test included in this panel only detects presence or absence of gray. The panel report does not provide the number of copies (zygosity) of the gray gene. If zygosity information is desired, please order the individual gray test.
 
INSTRUCTION VIDEO: How to pull hair for testing
 
Please Note: All DNA parentage verification and mandatory health testing results, whether purchased through the EBRA or transferred into the EBRA system, will become permanent record, which the documented owner may access at any time upon request. The EBRA is not responsible for providing non-mandatory DNA test results, therefore the release of any additional testing performed by past or present owners must be negotiated between the private parties at time of purchase.