Knabstrupper

Splashed White Mutations – SW1, SW2, SW3, SW4, SW5, SW6, SW7 and SW8

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 one or both blue eyes. Eight mutations in two different genes have been shown to cause the splashed white pattern.

Roan Zygosity Test

Classic Roan is a white patterning coat color trait characterized by intermixed white and pigmented hairs in the body while the head, lower legs, mane, and tail remain colored.

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.

Dominant White Mutations – W5, W10, W13, 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 five most common mutations known as W5, W10, W13, W20, and W22. Homozygosity for W5, W10, W13 or W22 is thought to be non-viable.

Cream

Cream is a dilution that causes the palomino, buckskin, smoky black, cremello, perlino, and smoky cream coat colors.

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.

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.

Fragile Foal Syndrome (FFS) Type I

Fragile foal syndrome (FFS) type I, formerly known as Warmblood fragile foal syndrome (WFFS) type I, is a recessive inherited connective tissue defect characterized by hyperextensible joints and abnormally thin fragile skin and mucous membranes.

Leopard Complex, Congenital Stationary Night Blindness, and Uveitis

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.