Equine coat color genetics determine a horse's coat color. There are many different coat colors possible, but all colors are produced by the action of only a few genes. The simplest genetic default color of all domesticated horses can be described as either "red" or "non-red", depending on whether a gene known as the "Extension" gene is present . When no other genes are active, a "red" horse is the color popularly known as a chestnut. Black coat color occurs when the Extension gene is present, but no other genes are acting on coat color.The Agouti gene can be recognized only in "non-red" horses; it determines whether black color is uniform, creating a black horse, or limited to the extremities of the body, creating a bay horse.
Chestnut and black are considered the "base" colors that all remaining coat color genes act upon. Bay (Agouti) is the most common modifier, restricting the black pigment to the points of the horse. There are a number of dilution genes that lighten these colors in a variety of ways, sometimes affecting skin and eyes as well as hair coat, including cream, dun, pearl, champagne and silver dapple. Genes that affect the distribution of white and pigmented coat, skin and eye color create patterns such as roan, pinto, leopard, white, and even white markings. Some of these patterns may be the result of a single gene, others may be influenced by multiple alleles. Finally the gray gene, which acts differently from other coat color genes, slowly lightens any other hair coat color to white over a period of years, without changing skin or eye color.
Much of the modern understanding of equine coat color genetics is owed to the work of Dr. Ann T. Bowling of the University of California, Davis and of Dr. Phillip Sponenberg of Virginia Polytechnic Institute. Modern discussions of horse coat color genetics are based on the distinction between "red" and "non-red" coats, a factor determined by a single gene. More detailed discussions of coat color all refer to the differing effects of separate genes on these "base" coat colors.
Coat color alleles affect melanin, the pigment or coloring of the coat. There are two chemically distinct types of melanin: pheomelanin, which is perceived as red to yellow color, and eumelanin, is perceived as brown to black. All coloration genes in mammals affect either the production or distribution of these two chemicals. Alleles affecting melanocytes (pigment cells) do not alter the pigment chemicals themselves but rather by acting on the placement of pigment cells produce distinct patterns of unpigmented pink skin and corresponding white hair.
Heritable characteristics are transmitted, encoded, and used through a substance called DNA, which is stored in almost every cell in an organism. DNA is organized into storage structures called chromosomes. For the most part, chromosomes come in matched sets, one chromosome from each parent. The location of a gene on a chromosome is called its locus. Alternate forms of a gene are called alleles. The terms Alleles and Modifiers are used interchangeably and describe the same concept. An allele identified with a capital letter is a dominant trait, one identified with a lower-case letter is a recessive trait. Because sex cells (sperm and ova) contain only half the usual number of chromosomes, each parent contributes one allele in each gene set to the ensuing offspring. When an individual's gene set contains two copies of the same allele, it is called homozygous for that gene. When it has two different alleles, it is heterozygous. For a recessive trait to be expressed, it must be homozygous, but a dominant trait will be expressed whether it is heterozygous or homozygous. A horse homozygous for a certain allele will always pass it on to its offspring, while a horse that is heterozygous carries two different alleles and can pass on either one.
Extension controls whether or not true black pigment (eumelanin) can be formed in the hair. True black pigment may be restricted to the points, as in a bay, or uniformly distributed in a black coat. Horses capable of producing eumelanin in the hair may have a genotype of either E/E or E/e. Horses without the ability to produce eumelanin in the hair always have the genotype e/e, and are most often chestnut or "red". The e allele is also sometimes called "red factor" and can be identified through DNA testing. Horses homozygous E/E are sometimes called "homozygous black", however depending on the color of the mate, E/E status confers no guarantee of black-coated offspring; only that no offspring will be "red".
The Extension locus is occupied by the melanocortin 1 receptor (Mc1r) gene, which encodes the eponymous protein. The MC1R protein straddles the membrane of pigment cells (melanocytes). MC1R picks up a chemical called alpha-melanocyte-stimulating hormone (α-MSH), which is produced by the body, from outside the cell. When MC1R comes into contact with α-MSH, a complex reaction is triggered inside the cell, and the melanocyte begins to produce black-brown pigment (eumelanin). Without the stimulation of α-MSH, the melanocyte produces red-yellow pigment (pheomelanin) by default.
Various mutations in the human Mc1r gene result in red hair, blond hair, fair skin, and susceptibility to sundamaged skin and melanoma. Polymorphisms of Mc1r also lead to light or red coats in mice, cattle, and dogs, among others. The Extension locus was first suggested to have a role in horse coat color determination in 1974 by Stefan Adalsteinsson. Researchers at Uppsala University, Sweden, identified a missense mutation in the Mc1r gene that resulted in a loss-of-function of the MC1R protein. Without the ability to produce a functional MC1R protein, eumelanin production could not be initiated in the melanocyte, resulting in coats devoid of true black pigment. Since horses with only one copy of the defective gene were normal, the mutation was labeled e or sometimes Ee. A single copy of the wildtype allele, which encodes a fully functional MC1R protein, is protective against the loss-of-function. The normal or wildtype allele is labeled E, or sometimes E+ or EE.
Agouti controls the restriction of true black pigment (eumelanin) in the coat. Horses with the normal agouti gene have the genotype A/A or A/a. Horses without a normal agouti gene have the genotype a/a, and if they are capable of producing black pigment, it is uniformly distributed throughout the coat. A third option, At, restricts black pigment to a black-and-tan pattern called seal brown. This allele is recessive to A and dominant to a, such that horses with the genotype A/At appear bay, while At/At and At/a horses are seal brown in the presence of a dominant Extension allele E.
The Agouti locus is occupied by the Agouti signalling peptide (Asip) gene, which encodes the eponymous protein (ASIP). Agouti signalling peptide is a paracrine signaling molecule that competes with alpha-melanocyte stimulating hormone (α-MSH) for melanocortin 1 receptor proteins (MC1R). MC1R relies on α-MSH to halt production of red-yellow pheomelanin, and initiate production of black-brown eumelanin in its place.
In many species, successive pulses of ASIP block contact between α-MSH and MC1R, resulting in alternating production of eumelanin and pheomelanin; hairs are banded light and dark as a result. In other species, Asip is regulated such that it only occurs in certain parts of the body. The light undersides of most mammals are due to the carefully controlled action of ASIP. In mice, two mutations on Agouti are responsible for yellow coats and marked obesity, with other health defects. Additionally, the Agouti locus is the site of mutations in several species that result in black-and-tan pigmentations. In normal horses, ASIP restricts the production of eumelanin to the "points": the legs, mane, tail, ear edges, etc. In 2001, researchers discovered a recessive mutation on Asip that, when homozygous, left the horse without any ASIP. As a result, horses capable of producing true black pigment had uniformly black coats. More recently, one coat color testing lab has begun offering a test for At. Further research remains to be seen.
Dun is one of several genes that control the saturation or intensity of pigment in the coat. Dun is unique in that it is simple dominant, affects eumelanin and pheomelanin equally, and does not affect the eyes or skin. Horses with the dominant D allele (D/D or D/d genotype) exhibit hypomelanism of the body coat, while d/d horses have otherwise intense, saturated coat colors. The mane, tail, head, legs, and primitive markings are not diluted. In some breeds, zygosity for Dun can be determined with an indirect DNA test.
While the Dun locus is known to be on equine chromosome 8, its precise location, the gene and protein involved, and exact mutation are not yet known. The molecular cause behind the dun coat colors is similarly not yet understood. The associated coat colors were assigned to the Dun locus in 1974 by Stefan Adalsteinsson, separate from Cream, with the presence of dun dilution indicated by the dominant D allele. The dominant D allele is relatively rare compared to the alternative d allele, and for this reason, the dominant allele is often treated as a mutation. However, the pervasive coat color among wild equids is in fact dun, and researchers from Darwin to modern day consider dun to be the wildtype state.
Cream is another one of the genes that control the saturation or dilution of pigment in the coat. Cream differs from Dun in that it affects the coat, skin, and eyes, and unlike Dun, is dosage dependent rather than simple dominant. Furthermore, the effects on eumelanin and pheomelanin are not equal. Horses with the homozygous recessive genotype (C/C) are not affected by cream. Heterozygotes (CCr/C) have one cream allele and one wildtype non-cream allele. Such horses, sometimes called "single-dilutes", exhibit dilution red pigment in the coat, eyes, and skin to yellow or gold, while eumelanin is largely unaffected. Homozygotes (CCr/CCr) have two cream alleles, and are sometimes called "double-dilutes." Homozygous creams exhibit strong dilution of both red and black pigment in the coat, eyes, and skin to ivory or cream. The skin is rosy-pink and the eyes are pale blue. Cream is now identifiable by DNA test.
The Cream locus is occupied by the Solute carrier family 45, member 2 (SLC45A2) gene, also called the Membrane associated transport protein or Matp gene. The Matp gene encodes a protein illustrated to have roles in melanogenesis in humans, mice, and medaka, though the specific action is not known.
Mutations in the human Matp gene result in several distinct forms of Oculocutaneous albinism, Type IV as well as normal variations in skin and hair color. Mice affected by a condition homologous to cream, called underwhite, exhibit irregularly shaped melanosomes, which are the organelles within melanocytes that directly produce pigment. The first descriptions of the dosage-dependent genetic control of the palomino coat color occurred early on in equine coat color inheritance research. However, the distinction between Dun and Cream remained poorly understood until Stefan Adalsteinsson wrote Inheritance of the palomino color in Icelandic horses in 1974. The mutation responsible, a single nucleotide polymorphism in Exon 2 resulting in an aspartic acid-to-asparagine substitution (N153D), was located and described in 2003 by a research team in France.
Champagne is a gene that controls the saturation or dilution of pigment in the coat. Unlike Cream, Champagne is not strongly dosage-dependent, and affects both types of pigment equally. Champagne differs from Dun in that it affects the color of the coat, skin, and eyes, and in that the unaffected condition is the wildtype. Horses with the dominant CH allele (CH/CH or CH/ch genotype) exhibit hypomelanism of the body coat, such that phaeomelanin is diluted to gold and eumelanin is diluted to tan. Affected horses are born with blue eyes which darken to amber, green, or light brown, and bright pink skin which acquires darker freckling with maturity. The difference in phenotype between the homozygous (CH/CH) and heterozygous (CH/ch) horse may be subtle, in that the coat of the homozygote may be a shade lighter, with less mottling. Horses with the homozygous recessive genotype (ch/ch) are not affected by champagne. Champagne is now identifiable by DNA test.
The Champagne locus is occupied by the Solute carrier family 36, member 1 (SLC36A1) gene, which encodes the Proton-coupled amino acid transporter 1 (PAT1) protein. This protein is one of many which is involved in active transport. The gene associated with the Cream coat colors is also a solute carrier, and orthologous genes in humans, mice, and other species are also linked to coat color phenotypes. The single nucleotide polymorphism responsible for the champagne phenotype is a missense mutation in exon 2, in which a C is replaced with a G, such that a threonine is replaced with arginine. This mutation was identified and described by an American research team in 2008.
|Locus||Alleles||Effect of combined pairs of alleles|
|EE or Ee: Horse forms black pigment in skin and hair.
ee: Horse is chestnut, it has black pigment in skin, but red pigment in hair.
|Agouti: Restricts eumelanin, or black pigment, to "points," allowing red coat color to show on body. No visible effect on red horses, as there is no black pigment to restrict.
AA or Aa horse is a Bay, black hair shows only in points pattern (usually mane, tail, legs, sometimes tips of ears).
aa: No agouti gene. If horse has E allele, then horse will be uniformly black.
|Cream gene The cream gene is an incomplete dominant.
|DD or Dd: Dun gene Another dilution gene. Horse shows a diluted body color to pinkish-red, yellow-red, yellow or mouse gray and has dark points including dorsal stripe, shoulder stripe and leg barring.
dd: Horse has undiluted coat color.
|Champagne: A rare but dominant dilution gene that creates pumpkin-colored freckled skin, amber, greenish, or blue eyes, and gives a bronze cast to hair. The skin surrounding the eye must be pink with freckles in adulthood.
ChCh or Chch: Champagne dilution evident (See Genetic Formulas Chart below.)
chch: No champagne dilution 
|ZZ or Zz: Silver dapple - Dilutes eumelanin or black pigment. Converts black to brown with white mane and tail or results in silver coloring.
zz: No silver dapple.
|Pearl: A new rare recessive dilution gene that looks very much like Champagne. The Pearl gene is sometimes referred to as the "barlink factor." One dose of the mutation does not change the coat color of black, bay or chestnut horses. Two doses on a chestnut background produce a pale, uniform apricot color of body hair, mane and tail. Skin coloration is also pale. Pearl is known to interact with Cream dilution to produce pseudo-double Cream dilute phenotypes including pale skin and blue/green eyes.
PrlPrl or Prlprl: No pearl dilution.
prlprl: Pearl dilution evident.
|TOTO or TOto: Tobiano, a form of pinto patterning. Produces regular and distinct ovals or rounded patterns of white and color with a somewhat vertical orientation. White extends across the back, down the legs, but face and tail are usually dark.
toto: No tobiano pattern present.
|O Also noted as Fr or FrO||O
|Oo: Frame Overo pattern - Pinto horse pattern that forms a solid frame around white spotting. White is usually horizontal in orientation with jagged edges, color crosses the back and legs, face is often white. The Overo "O" allele is different from overo as a color pattern classification in those registries which also include the splashed white and sabino genes under the heading "overo."
oo: No overo pattern present.
OO: Homozygous overo is lethal white syndrome, characterized by an incomplete colon and the inability to defecate, which leads to death or humane euthanization within days of birth.
WW: Lethal. Embryo reabsorbed or fetus dies en utero.
|GG or Gg: gray gene. Horse shows progressive silvering with age to white or flea-bitten, but is born a non-gray color. Pigment is always present in skin and eyes at all stages of silvering. Gray horses range from white to dark gray depending on age and the proportion of white hairs in the coat. Horses' coats gray in a manner similar to graying in human hair.
gg: Horse does not gray with aging.
|RnRn or Rnrn: roan pattern of white hair mixed in with base color. There quite likely is no lethal roan question.
rnrn: No roan pattern.
|Sabino - Assorted pinto or roan-like markings.
Sabino may be polygenic (a gene-complex rather than a single gene pair), caused by several different genes. Recognized by abundant white on the legs, belly spots or body spots that are can be flecked and roaned, chin spots, or white on the face extending past the eyes. Sabino is registered as overo by some registries, but is not the overo or frame overo allele. No risk of lethal white, though some "Fully expressed" sabinos may be completely white in coat color.
SbSb or Sbsb: Sabino markings.
sbsb: No sabino markings.
SB1:The only Sabino gene currently detected by DNA testing, however does not appear to be the gene that creates sabino coloring in Arabians or Clydesdales.
|Appaloosa or Leopard spotting gene. Produces coat spotting patterns, mottling over otherwise dark skin, striped hooves and white sclera around the eye.|
|Bay double pearl||E/-||A/-||d/d||ch/ch||z/z||cr/cr||prl/prl|
|Black double pearl||E/-||a/a||d/d||ch/ch||z/z||cr/cr||prl/prl|
|Wikimedia Commons has media related to Horse coat colors.|
If a horse has black hair in either of these patterns, then the animal possesses an allele of the E gene which contains the instructions for placing black pigment in hair. Geneticists symbolize this allele of the E gene E. The alternative allele to E is e. Allele e allows black pigment in the skin but not in the hair. The pigment conditioned by the e allele makes the hair appear red
A statistically significant tendency (X249.1; p < 0.01) of lighter bay shades carrying the EE/Ee genotype (35 of 42 bay horses) and darker bay shades carrying the EE/EE genotype (9 of 16 dark bay horses) was found in our panel. Thus, lighter bay shades would be at least partially explained by a dosage effect of an average 50% less working melanocortin-1-receptor function due to the Ee-allele (Table 2). However, this result might be biased by the structure of our horse panel and presently unknown genetic variationCite uses deprecated parameter
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)