The champagne gene is a simple dominantallele responsible for a number of rare horsecoat colors. The most distinctive traits of horses with the champagne gene are the hazel eyes and pinkish, freckled skin, which are bright blue and bright pink at birth, respectively. The coat color is also affected: any hairs that would have been red are gold, and any hairs that would have been black are chocolate brown. If a horse inherits the champagne gene from either or both parents, a coat that would otherwise be chestnut is instead gold champagne, with bay corresponding to amber champagne, seal brown to sable champagne, and black to classic champagne. A horse must have at least one champagne parent to inherit the champagne gene, for which there is now a DNA test.
Unlike the genes underlying tobiano, dominant white, frame overo spotting and the Leopard complex common to the Appaloosa, the champagne gene does not affect the location of pigment-producing cells in the skin. Nor does the champagne gene remove all pigment from the skin and hair, as in albinism. Instead, the champagne gene produces traits known as hypomelanism, or dilution. Champagne is not associated with any health defects. Other dilution genes in horses include the Cream gene, Dun gene, Pearl gene and Silver dapple gene. Horses affected by these genes can sometimes be confused with champagnes, but champagnes are genetically distinct. Champagnes are not palominos, buckskins, or grullos, nor does the word champagne indicate that a horse is a shiny or light shade of another coat color.
This gene and the associated coat colors are only known in American breeds, especially the American Cream Draft, Tennessee Walker, American Saddlebred and Missouri Fox Trotter. The Source of this Gen is found in very old pony horses of Tibet Plateau e.g. Yushu Horse, Debao Pony and others, perfect for hypomelanism.
Coat colors
Classic champagne, black base diluted by champagne gene.Amber champagne, bay base diluted by champagne gene.Gold champagne, chestnut base diluted by champagne gene. Note similarity to palomino, but distinguished by mottling around nose
Champagne is a dominant trait, based on a mutation in the SLC36A1 gene.[1] A horse with either one or two champagne genes will show the effects of the gene equally. However, if a horse is homozygous for a dominant gene, it will always pass the gene on to all of its offspring, while if the horse is heterozygous for the gene, the offspring will not always inherit the color. Horses with the champagne gene may also carry other coat color genes that affect their phenotype, or outward color.
Horses with the champagne gene have a lightened hair coat and specific eye and skin color traits. Black pigment in the coat, if present, is lightened to chocolate, while red pigment is lightened to gold. The precise champagne dilute coat color produced depends on the underlying base coat color. The effects of champagne plus additional coat color genes have their own distinct vocabulary and appearances;
It is difficult to distinguish between homozygous and heterozygous champagne, which is different from incomplete dominant dilutions such as the cream gene. However the 2008 study that mapped the gene and identified it as a dominant trait noted in passing that homozygotes may have less mottling or a slightly lighter hair color.[2] The authors of this study noted that
The following are considered the most "basic" champagne coat colors:
Classic champagne is, as its name suggests, the coat color most associated with the champagne gene. It is produced by the action of champagne on a black coat. The body coat is chocolate, the mane and tail a darker shade. The legs may also be slightly darker. The overall effect has also been described as lilac, dark taupe, and even green.[3][4] This color is most often misclassified as grullo, and in the past was sometimes called "lilac dun."
Sable champagne is produced by the action of champagne on a seal brown coat.[5] It is visually difficult to distinguish from classic champagne, and can be confirmed by a DNA test negative for the recessive black (a) allele at Agouti.[5]
Amber champagne is produced by the action of champagne on a bay coat. The coat is gold with chocolate points. Just as there are varying shades of bay, the gold body coat may vary in shade as well.[6] The legs are often lighter than the mane and tail, and the colored points may be difficult to see. The mane and tail may also have "frosting" or light edges, a trait that also occurs in bay duns and some buckskins.[7] Amber champagne can be confused with buckskin or bay dun.
Gold champagne is produced by the action of champagne on a chestnut coat. The coat is gold, and the mane and tail are typically ivory. In some cases, the mane and tail may be self-colored, matching the body coat. These gold champagnes are sometimes called "dark gold" and may be an all-over apricot shade.[8][9] Dark gold champagnes can be confused with red dun, while those with paler manes and tails were historically called "pumpkin-skinned palominos."
Apart from the unique shades, there are several qualities of the champagne coat that may be used to help identify them. Champagne coats often have an unusual sheen.[10] This sheen makes champagnes difficult to photograph accurately, as the appearance of the coat depends on the lighting.[3] Not all champagne horses have this sheen, and there are many extremely shiny non-champagne horses, so a "sheen" in and of itself does not indicate the champagne gene.[11] The coat may also exhibit reverse dappling, though this is also an unreliable indicator.[11]
Skin, eyes, and hooves
The tell-tale identifiers of the champagne gene in an adult horse are hazel eyes and freckled skin.At birth, champagne horses have bright blue eyes and bright pink skin, as the horse matures the eyes darken to hazel and the skin becomes freckled.
The color of the skin is the single most important visual identifier of champagne horses: in the adult horse, the skin is "pink with abundant dark freckles, except under white markings."[11] The freckles - not mottles, splotches, specks, or blotches - are dark and may have a purple cast, and are small and numerous. By comparison, mottling associated with the Leopard complex is large and blocky alternations between true black or charcoal-colored skin and pigmentless-pink skin. The skin of cremellos and perlinos is pigmented-pink, and exhibit a scant few tiny black specks. Homozygous pearls and pearl-cream combinations also exhibit some freckling of the skin, however this is muted in comparison to the freckles of champagne skin.[11] The skin may exhibit an overall lavender tone.[1] The color qualities of the skin are most evident around the eyes and muzzle, under the tail, and on the udder or sheath.[1]
The eyes of an adult champagne horse are most often described as hazel or amber.[12] In the newborn or very young foal, the eyes are bright blue to blue-green and the skin is bright pink.[1][13] The champagne blue foal eye is creamier than other types of blue eye such as the bright, unpigmented blue seen on some pinto horses.[14]
In the past, some breeders and horse owners had concerns that horses with light-colored skin and eyes were not healthy. However, the lightening of these parts of the horse due to the champagne gene is not known to be linked to any health or genetic defects. While horses with white markings may sunburn on exposed unpigmented skin, the freckled-pink skin of a champagne horse is said to tan instead.[15] In addition, the color of the hoof has no bearing on its strength.[16]
Interaction with other coat color factors
The presence of other coat color modifying alleles has no effect on whether or not a horse has the champagne trait. However, different traits may interact; they may suppress, enhance, obscure or cancel out various tell-tale clues to the genetic identity of a coat color. Coat colors involving multiple genes often have an unexpected appearance and unique terminology. This type of genetic interaction is called epistasis.
Horses with both the champagne gene and the cream gene are the most common combination. The cream gene is responsible for the palomino, buckskin and cremello coat colors, and is a dose-dependent or incomplete dominant, meaning that a horse with only one copy is visibly different from a horse with two copies of the gene. A single copy of the cream gene dilutes red pigment in the coat to gold or yellow, and has a slight effect on the skin and eye color. The black pigment is lightened little, if at all. Two copies of the cream gene dilute both red and black pigments in the hair to cream or ivory, dilute the skin to a rosy-pink and the eyes to pale blue. The cream gene and champagne gene have an additive or enhancing interaction. Horses with the champagne gene and a single cream gene typically have lighter yellowish or blue eyes and paler, more faintly freckled skin.[17]
Gold cream or Ivory champagne refers to an otherwise-chestnut coat affected by the champagne gene and a single copy of the cream gene.[18] The mane, tail, and coat of gold creams are typically ivory and difficult to distinguish from cremello, other than by the skin and eyes.
Amber cream, similarly, is an otherwise-bay coat affected by the champagne gene and a single copy of the cream gene.[18] The mane and tail of a typical amber cream are a warm yellowish-brown and are often frosted. The legs may also be a light chocolate brown, but need not be. The body coat is a shade of ivory, usually darker than a gold cream. Their points are substantially darker than those of a perlino, and they have champagne skin and eye traits.
Sable cream is a seal brown coat affected by champagne and a single copy of the cream gene.[18] Sable creams may more closely resemble amber cream or classic cream. Most are several shades darker, with a cooler hue, than amber creams.
Classic cream is a black coat affected by champagne and a single copy of the cream gene.[18] Classic cream coats should resemble classic champagne shades, being only slightly lightened by the cream gene. Their coats may have a cooler hue.
Double cream champagne is a coat of any color affected by champagne and both copies of the cream gene.[18] Unlike the coat colors associated with only a single cream gene, double cream champagnes (respectively prefixed with "gold," "amber," etc.) retain no obvious champagne traits. Their skin is clear pink without freckling, and the eyes are pale blue.[19] The terms "cremello champagne", "perlino champagne" and so forth are also acceptable.
Horses with both the champagne gene and the dun gene are also well-recorded. The dun gene is responsible for flat, diluted coat colors and vivid primitive markings. Bay dun is thought to be the wildtype horse coat color. Dun does not affect skin or eye color, but dilutes red pigment to yellow and black pigment to slate gray. Champagne horses with the dun gene will have slightly further-diluted coats compared to non-dun champagnes, and will always exhibit striking primitive markings, such as a dorsal stripe and zebra-like stripes on the legs. [20] Naming schemes are much the same as with champagne-cream combinations. Champagne-dun combinations retain their champagne eye and skin traits. The coats are distinguishable from non-champagne duns in that they are several shades lighter, black pigment is chocolate rather than slate, and they may exhibit a sheen. The coats are distinguishable from non-dun champagnes in the presence of primitive markings and a flatter tone.
Gold dun refers to an otherwise-chestnut coat affected by both the champagne gene and dun gene.[21] The mane and tail may be ivory or self-colored; the body coat ranges from a warm cream to apricot color with primitive markings a shade darker. The coat is substantially paler and more "yellow" than that of a chestnut dun, and flatter than that of a gold champagne.
Amber dun refers to an otherwise-bay coat affected by both the champagne gene and dun gene.[21] The mane and tail and primitive markings are warm chocolate brown with a buff tan-colored body. The legs may, or may not, be dark as well.
Sable dun refers to an otherwise-seal brown coat affected by both the champagne gene and dun gene.[21] The points are chocolate-colored and the coat is darker than the amber dun.
Classic dun or Classic grulla refers to an otherwise-black coat affected by both the champagne gene and dun gene.[21] The coat possesses more cool slate-gray tones than a classic champagne, while the points are warmer than a grulla.
The silver dapple gene in horses does not affect the eyes, skin, or red pigment. Chestnuts are unaffected, but in bay, seal brown, and black horses, the black pigment is diluted to a chocolate or silver. The mane and tail are most commonly affected. Champagne horses with the silver gene will retain their champagne skin and eye traits, but the black pigment will be further diluted.[22] Silvers vary tremendously in shade and so defining a "typical" example is difficult.
Amber silver refers to an otherwise-bay coat affected by both the champagne gene and silver gene.[23] The interaction of these two genes - one diluting black to warm chocolate and red to gold, and the other diluting black further to silver - creates an unexpected phenotype. The more closely resembles colors in the red family, mostly deprived of black pigment. The mane and tail may be self-colored, and the coat is buttery and pale.
Classic silver refers to an otherwise-black coat affected by both the champagne gene and silver gene.[23] The darkest examples resemble classic champagnes with a silvery mane and tail. The palest are a very pale pewter. Some have warm chocolate tones, others do not.
The champagne gene, in combination with some white patterning genes, can also produce unexpected phenotypes. Horses with the leopard gene or Appaloosas exhibit starkly mottled skin around the muzzle, eyes, anus and sheath or udder. Most commonly, the mottling is blocky patches of normal, black skin and unpigmented pink. When a horse has both the leopard gene and the champagne gene, the champagne-associated skin is present only where the skin would be otherwise black.[24]
In combination with gray, champagne produces very unusual coat behavior. Typically, gray horses are born a dark shade of their natural color, and begin to develop gray hairs around the eyes and muzzle. With each shed, the coat becomes lighter and lighter. Many older grays develop the "fleabitten" trait, in which small, interspersed flecks of red occur and often increase in density with age, even as the rest of the coat loses pigment. A few grays will also develop vitiligo in which the skin also progressively loses pigment. When a horse carries both gray and champagne, additional traits occur: Gray-champagnes are born with darker coats than the usual champagne foal, but still exhibiting the expected bright blue eyes and pink skin. The freckling that develops on the skin is also exceptionally dark and dense. Gray-champagnes appear more likely to experience vitiligo.[11] The most unexpected quality of gray-champagnes is the intensity of the fleabitten trait. Flecks of champagne-colored hair are thickly interspersed in the unpigmented white hairs.[25]
Champagne mimics
Many coat color modifying genes affect the skin and eyes as well as the coat color. Several of these may be confused with champagne. Today, when the visible cues are insufficient, horses can be DNA tested for the champagne gene, Cream gene, Pearl gene, and Silver dapple gene.
Palomino or Chestnut vs. Gold champagne: The most common confusion, as both of these genetically distinct coat colors feature a gold or yellow coat and ivory or cream mane and tail. As adults, the pinkish freckled skin and hazel eyes indicate gold champagne, while gray or black skin and light or dark brown eyes indicate palomino. At birth, palominos may have pink skin and blue or grey eyes, however these darken within days or weeks.[26] Occasionally, chestnuts are also born with blue eyes and pink skin, and as gold champagnes often have chestnut-colored foal coats, the two can be difficult to distinguish. Again, the skin and eyes of the chestnut will darken quickly.[27] In all cases, pedigrees can provide important information. Palominos will have a parent that is palomino, buckskin, smoky black, or blue-eyed cream. Champagnes will have a champagne parent.
Buckskin and Bay dun vs. Amber champagne: All three of these genetically distinct coat colors feature a lighter bronze or tan coat with darker points. As adults, the pinkish freckled skin and hazel eyes indicate amber champagne, while gray or black skin and light or dark brown eyes indicate buckskin or bay dun. Duns do not exhibit unusually colored skin, though buckskins, like palominos, may be born with blue eyes that darken within days or weeks.[27] In the adult, the points of a buckskin or bay dun will be black, not chocolate as in the amber champagne.[28] Bay dun horses also exhibit primitive markings, especially a dorsal stripe, though amber duns will also possess these marks. The eyes and skin remain the best identifying feature. Buckskins, like palominos, will a parent that is palomino, buckskin, smoky black, or blue-eyed cream. Bay duns will have a parent that is bay dun, red dun, or grullo. Champagnes will have a champagne parent.
Grullo vs. Classic champagne or Sable champagne: Classic and sable champagnes are difficult to distinguish without a DNA test. Grullos and classic champagnes are both dilutions of the black coat, and typically have black or dark points and dove-gray coats. However, Grullos, in absence of any other dilution factors, are not born with pink skin and blue eyes, while champagnes always have these traits. As adults, grullos will retain their dark brown eyes and black skin, while champagnes have pinkish freckled skin and hazel eyes. Grullos, like all duns, will possess primitive markings, and their coats are typically a cooler, slate shade, while classic and sable champagnes are chocolate-toned. The points and primitive markings on the grullo are black, while the points on classic and sable champagnes are brown. Grullos will have dun ancestry and champagnes will have champagne ancestry.
Red dun vs. Dark gold champagne: Some gold champagnes have darker bodies and self-colored manes and tails. These horses may resemble red duns, however red duns have distinct primitive markings and do not possess pinkish freckled skin or hazel eyes as adults, nor the bright pink skin and bright blue eyes of champagne foals.[11]
Blue-eyed cream vs. Champagne: Blue-eyed cream is a collective term for any horse homozygous for the Cream gene (cremello, perlino, etc.). Blue-eyed creams, as their name suggests, have blue eyes from birth through adulthood and also have pink skin. Typically their blue eyes are quite pale, and are easy to distinguish from the sky blue eyes of champagne foals and the hazel eyes of adult champagnes. Their skin may have a scant few black flecks, but the abundant freckles of champagne skin are absent. The respective shades of pink skin and blue eyes are slightly different.[11]
Leopard complex has a different mottling pattern from champagne's freckling pattern
Leopard vs. Champagne: The Leopard complex is responsible for the spotted coat of the Appaloosa and other breeds. Even when a spotted hair coat is absent, other traits produced include mottled skin and a white sclera around the eye but generally the eye itself is dark brown. These mottles are alternations between unpigmented pink skin and pigmented skin, which is usually black (thus the mottles are black on a pink background). The mottles are substantially larger than the freckles of champagne skin, and leopard complex horses do not necessarily have light eyes.[11]
Pearl vs. Champagne: In the homozygous state, or when combined with cream, the Pearl gene produces a diluted apricot to buff color, pale eyes and pale skin. Heterozygous pearls (one copy of the gene) often exhibit dark skin with some pinkish freckles, while homozygous pearls (two copies of the gene) have champagne-like skin. The freckles on homozygous pearls and pearl-creams are pale and muted.[11]
Most American Cream Draft horses owe their consistently reproducible coat color to the champagne gene.
The champagne gene was located in 2008, but is not a new mutation. It is widespread among American horses, and has likely been present in the genepool for more than a century. The Palomino Horse Breeders Association (PHBA), which registers "palomino" horses based on appearance, includes allowances for freckle-skinned and hazel-eyed palominos. Furthermore, while the registry typically disallows horses with pink skin, it allows American Saddlebreds with skin of any color to be registered.[31] The PHBA was incorporated in 1941. Further back, the foundation mare of the American Cream Draft horse breed, "Old Granny", was born around 1905 in Iowa.[29] Her cream-colored coat, pink skin and amber eyes are defining standards for the breed of her descendants, which are now known to be gold champagne.[32] The superficial similarities between gold champagne and palomino, and amber champagne and buckskin, may account for the relatively recent identification of champagne as a separate trait. Gold champagnes were sometimes called "pumpkin-skinned palomino."[33] Classic champagnes, which lack the primitive markings of true duns, were similarly called "lilac duns."[34] The mare that brought the champagne coat color family to the attention of modern researchers was a Tennessee Walking Horse named "Champagne Lady Diane" born in 1969. A classic champagne, Champagne Lady Diane was described as "a genetic color accident" after her hairs were sent to several universities, although current evidence suggests that the champagne gene predates Champagne Lady Diane.[35]
This classic champagne Tennessee Walking Horse illustrates the unusual sheen common to many champagnes.
It was not until many years after the name "champagne" was ascribed to Champagne Lady Diane that the term appeared in scientific literature. It was first studied and described by Sponenberg and Bowling in 1996. They studied the ratio of champagne-to-non-champagne offspring of champagne horses, and designated the causal mutation as the dominant Ch allele on the hypothetical Champagnelocus.[36]
Inheritance and expression
The champagne locus is on exon 2 of the SLC36A1 gene, which is on chromosome 14 (ECA14); a single nucleotide polymorphism (SNP) exchanges a C for a G at base 76 (c.188C>G) resulting in a missense mutation. On a protein level, this SNP is predicted to result in the replacement of a threonine with arginine at amino acid 63 (T63R).[37]SLC36A1 is not associated with pigmentation phenotypes in other species, and its role in most tissues is poorly understood.[38]SLC36A1 is a member of a loosely united group of over 300 proteins responsible for active transport and facilitated diffusion called the Solute carrier family. Other members of this family include SLC45A2, which is responsible for pigmentation variations of many types in humans, as well as the cream coat color in horses; and SLC24A5, which is responsible for the Golden dilution in mice.[39]
Dilution genes such as champagne and cream affect the nature or density of the pigments produced by melanocytes. On the other hand, genes in horses which produce white spotting, such as Frame and Sabino1, interrupt or limit the migration of melanocytes from the neural crest. In other words, the skin, eyes, and hair of horses with the champagne mutation do not lack melanocytes, melanosomes, or melanins, but rather exhibit hypomelanism. However, the specific role of SLC36A1 in pigmentation and how the champagne coat colors are created on a molecular level is not known. The researchers who identified the mutation in 2008 suggested that melanosomepH may be affected, which in turn might affect the processing of tyrosine, a critical element of melanogenesis.[40]
There are two alleles in this series: the recessive, wildtype allele ch and the dominant CH.[36] The CH allele represents the T63R SLC36A1 mutation.
ch/ch recessive homozygotes are not affected by champagne and have no true champagne traits.
CH/ch heterozygotes have one champagne allele, and one wildtype non-champagne allele. The skin is bright pink and the eyes bright blue at birth, darkening to freckled and hazel with age, respectively. Both red and black pigment in the hair are diluted.
CH/CH homozygotes (homozygous champagnes) have no wildtype non-champagne alleles. Such horses are indistinguishable from heterozygotes, except that their freckles may slightly sparser and the coat slightly lighter.[41]
The DNA test for champagne detects the c.188C>G mutation on SLC36A1.[1]
Palomino is a genetic color in horses, consisting of a gold coat and white mane and tail; the degree of whiteness can vary from bright white to yellow. The palomino color derived from the inter-breeding of Spanish horses with those from the United States. Genetically, the palomino color is created by a single allele of a dilution gene called the cream gene working on a "red" (chestnut) base coat. Palomino is created by a genetic mechanism of incomplete dominance, hence it is not considered true-breeding. However, most color breed registries that record palomino horses were founded before equine coat color genetics were understood as well as they are today, therefore the standard definition of a palomino is based on the visible coat color, not heritability nor the underlying presence of the dilution gene.
The American Paint Horse is a breed of horse that combines both the conformational characteristics of a western stock horse with a pinto spotting pattern of white and dark coat colors. Developed from a base of spotted horses with Quarter Horse and Thoroughbred bloodlines, the American Paint Horse Association (APHA) breed registry is now one of the largest in North America. The registry allows some non-spotted animals to be registered as "Solid Paint Bred" and considers the American Paint Horse to be a horse breed with distinct characteristics, not merely a color breed.
A dilution gene is any one of a number of genes that act to create a lighter coat color in living creatures. There are many examples of such genes:
Bay is a hair coat color of horses, characterized by a reddish-brown or brown body color with a black point coloration on the mane, tail, ear edges, and lower legs. Bay is one of the most common coat colors in many horse breeds.
At right is displayed the color traditionally called liver.
Point coloration is animal coat coloration with a pale body and relatively darker extremities, i.e. the face, ears, feet, tail, and scrotum. It is most recognized as the coloration of Siamese and related breeds of cat, but can be found in dogs, rabbits, rats, sheep, guinea pigs and horses as well.
A gray horse has a coat color characterized by progressive depigmentation of the colored hairs of the coat. Most gray horses have black skin and dark eyes; unlike some equine dilution genes and some other genes that lead to depigmentation, gray does not affect skin or eye color. Gray horses may be born any base color, depending on other color genes present. White hairs begin to appear at or shortly after birth and become progressively more prevalent as the horse ages as white hairs become intermingled with hairs of other colors. Graying can occur at different rates—very quickly on one horse and very slowly on another. As adults, most gray horses eventually become completely white, though some retain intermixed light and dark hairs.
The cream gene is responsible for a number of horse coat colors. Horses that have the cream gene in addition to a base coat color that is chestnut will become palomino if they are heterozygous, having one copy of the cream gene, or cremello, if they are homozygous. Similarly, horses with a bay base coat and the cream gene will be buckskin or perlino. A black base coat with the cream gene becomes the not-always-recognized smoky black or a smoky cream. Cream horses, even those with blue eyes, are not white horses. Dilution coloring is also not related to any of the white spotting patterns.
The silver or silver dapple (Z) gene is a dilution gene that affects the black base coat color and is associated with Multiple Congenital Ocular Abnormalities. It will typically dilute a black mane and tail to a silvery gray or flaxen color, and a black body to a chocolaty brown, sometimes with dapples. It is responsible for a group of coat colors in horses called "silver dapple" in the west, or "taffy" in Australia. The most common colors in this category are black silver and bay silver, referring to the respective underlying coat color.
Equine coat color genetics determine a horse's coat color. Many colors are possible, but all variations are produced by changes in only a few genes. Bay is the most common color of horse, followed by black and chestnut. A change at the agouti locus is capable of turning bay to black, while a mutation at the extension locus can turn bay or black to chestnut.
The dun gene is a dilution gene that affects both red and black pigments in the coat color of a horse. The dun gene lightens most of the body while leaving the mane, tail, legs, and primitive markings the shade of the undiluted base coat color. A dun horse always has a dark dorsal stripe down the middle of its back, usually has a darker face and legs, and may have transverse striping across the shoulders or horizontal striping on the back of the forelegs. Body color depends on the underlying coat color genetics. A classic "bay dun" is a gray-gold or tan, characterized by a body color ranging from sandy yellow to reddish brown. Duns with a chestnut base may appear a light tan shade, and those with black base coloration are a smoky gray. Manes, tails, primitive markings, and other dark areas are usually the shade of the undiluted base coat color. The dun gene may interact with all other coat color alleles.
Chestnut is a hair coat color of horses consisting of a reddish-to-brown coat with a mane and tail the same or lighter in color than the coat. Chestnut is characterized by the absolute absence of true black hairs. It is one of the most common horse coat colors, seen in almost every breed of horse.
Horses exhibit a diverse array of coat colors and distinctive markings. A specialized vocabulary has evolved to describe them.
A white horse is born predominantly white and stays white throughout its life. A white horse has mostly pink skin under its hair coat, and may have brown, blue, or hazel eyes. "True white" horses, especially those that carry one of the dominant white (W) genes, are rare. Most horses that are commonly referred to as "white" are actually "gray" horses whose hair coats are completely white. Gray horses may be born of any color and their hairs gradually turn white as time goes by and take on a white appearance. Nearly all gray horses have dark skin, except under any white markings present at birth. Skin color is the most common method for an observer to distinguish between mature white and gray horses.
Black is a hair coat color of horses in which the entire hair coat is black. It is not uncommon to mistake dark chestnuts or bays for black.
The American Cream Draft is an American breed of draft horse, characterized by the cream or "gold champagne" color of its coat. It was developed in Iowa during the early twentieth century from a cream-colored mare named Old Granny. A breed registry was formed in 1944 but became inactive for several decades when breed numbers dropped due to the mechanization of farming. It was reactivated in 1982 and population numbers have slowly grown since then. It is a rare breed: its conservation status is considered critical by The Livestock Conservancy and the Equus Survival Trust.
Smoky black or black carrying cream is a coat color of horses which has the same phenotype as black. Smoky black is produced by the action of a heterozygous cream gene on an underlying black coat color. Therefore, smoky black is a member of the cream family of coat color dilutions, and found in horse populations that have other cream-based colors such as palomino, buckskin, perlino, cremello and smoky cream. All smoky blacks must have at least one parent with the cream gene, and a smoky black can only be verified through DNA testing or parentage. Smoky black has been mistaken for faded black, dark bay or brown, grullo or even liver chestnut.
The Pearl gene, also known as the "Barlink factor", is a dilution gene at the same locus as the cream gene, which somewhat resembles the cream gene and the champagne gene but is unrelated to champagne. It is a somewhat rare dilution gene found in the American Quarter Horse, American Paint Horse, and Peruvian Paso. The same mutation appears in Iberian horse breeds such as the Lusitano and Andalusian. The existence of the pearl gene in Quarter Horses and Paints is probably because these breeds have some Iberian ancestors.
Seal brown is a hair coat color of horses characterized by a near-black body color; with black points, the mane, tail and legs; but also reddish or tan areas around the eyes, muzzle, behind the elbow and in front of the stifle. The term is not to be confused with "brown", which is used by some breed registries to refer to either a seal brown horse or to a dark bay without the additional characteristics of seal brown.
Flaxen is a genetic trait in which the mane and tail of chestnut-colored horses are noticeably lighter than the body coat color, often a golden blonde shade. Manes and tails can also be a mixture of darker and lighter hairs. Certain horse breeds such as the Haflinger carry flaxen chestnut coloration as a breed trait. It is seen in chestnut-colored animals of other horse breeds that may not be exclusively chestnut.
↑ "Classic Champagne". Classifications. Champagne Horse Breeders and Owners Association. Archived from the original on 2008-05-09. Retrieved 2009-06-08.
↑ Cook et al. 2008. "To be characterized as possessing the champagne phenotype, horses exhibited a diminished intensity of color (dilution) in black or brown hair pigment and met at least two of the three following criteria: 1) mottled skin around eyes, muzzle and/or genitalia, 2) amber, green, or light brown eyes, or 3) blue eyes and pink skin at birth"
↑ Cook et al. 2008. "champagne foals are born with blue eyes, which change color to amber, green, or light brown and pink "pumpkin skin" which acquires a darker mottled complexion around the eyes, muzzle, and genitalia as the animal matures. Foals with one copy of CR also have pink skin at birth but their skin is slightly darker and becomes black/near black with age."
↑ Identifying the Champagne Colored Horse. "The pink skin of a Champagne horse is "pigmented pink" -- not the pigment-free, paler pink color found under all white markings of all horses. It will often tan."
↑ Runicman, RJ; JJ Thomason; G Springett; S Bullock; W Sears (November 2004). "Horseshoe Fixation versus Hoof Colour, a Comparative Study". Biosystems Engineering. 89 (3). Elsevier: 377–382. Bibcode:2004BiSyE..89..377R. doi:10.1016/j.biosystemseng.2004.08.005. For the remainder of the hooves included in this study, colour did not appear to have a strong effect on the resistance to nail extraction and hence shoe fixation
↑ "Champagne Cream". Classifications. Champagne Horse Breeders and Owners Association. Archived from the original on 2007-08-11. Retrieved 2009-06-06.
↑ "Champagne Silver". Classifications. Champagne Horse Breeders and Owners Association. Archived from the original on 2008-05-09. Retrieved 2009-06-06.
↑ "Champagne + Gray". International Champagne Horse Registry. Retrieved 2009-06-06.
↑ "Gold vs. Palomino". Champagne Comparisons. Champagne Horse Breeders and Owners Association. Archived from the original on 2008-05-09. Retrieved 2009-06-09.
↑ "Amber vs. Buckskin". Champagne Comparisons. Champagne Horse Breeders and Owners Association. Archived from the original on 2008-05-09. Retrieved 2009-06-09.
1 2 "Home". American Cream Draft Horse Association. Archived from the original on 2011-02-14. Retrieved 2009-06-03.
↑ "Our History". American Cream Draft Horse Association. Archived from the original on 2011-02-14. Retrieved 2010-10-24.
↑ Champagne Horse Breeders and Owners Association (2007-05-26). "The Genetics of Champagne Coloring". The Horse. Retrieved 2009-06-04. Prior to this the champagne gene was often misidentified. Many champagnes were mistakenly called "pumpkin-skinned palominos"...
↑ . p.46. Lilac dun has been used for some of these colors in the past...{{cite book}}: Missing or empty |title= (help)
↑ Cook, D; Brooks S; Bellone R; Bailey E (2008). Barsh, Gregory S. (ed.). "Missense Mutation in Exon 2 of SLC36A1 Responsible for Champagne Dilution in Horses". PLOS Genetics. 4 (9): e1000195. doi:10.1371/journal.pgen.1000195. PMC2535566. PMID18802473. Only one SNP was found, a missense mutation involving a single nucleotide change from a C to a G at base 76 of exon 2 (c.188C>G) (Figure 5). These SLC36A1 alleles were designated c.188[C/G], where c.188 designates the base pair location of the SNP from the first base of SLC36A1 cDNA, exon 1. Sequencing traces for the partial coding sequence of SLC36A1 exon 2 with part of the flanking intronic regions for one non-champagne horse and one champagne horse were deposited in GenBank with the following accession numbers respectively: EU432176 and EU432177. This single base change at c.188 was predicted to cause a transition from a threonine to arginine at amino acid 63 of the protein (T63R)
↑ Online Mendelian Inheritance in Man, OMIM (TM). Johns Hopkins University, Baltimore, MD. MIM Number: 606561: 4/22/2004: World Wide Web URL: https://www.ncbi.nlm.nih.gov/omim/
↑ Cook et al 2008. "...the gene responsible for the cream dilution phenotypes in horses, SLC45A2 (MATP), belongs to a similar solute carrier family. In humans, variants in SLC45A2 have been associated with skin color variation...SLC24A5 is responsible for the Golden (gol) dilution as mentioned in the review of mouse pigment research by Hoekstra (2006)"
↑ Cook et al 2008. "Since organellular pH affects tyrosine processing and sorting [18], an amino acid substitution in this protein may affect pH of the early stage melanosome and the ability to process tyrosine properly."
↑ Cook et al 2008. "The homozygote may differ by having less mottling or a slightly lighter hair color than the heterozygote."
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