Roan (RN)
Gene or Region: KIT
Reference Variant: N
Mutant Variant: RN1, RN2, RN3 (multiple markers)
Affected Breeds: American Quarter Horse, Gypsy, Noriker, and many more
Research Confidence: High - Strong association in studied populations
Explanation of Results: RN/RN = homozygous for Roan, white ticking and interspersed white hairs throughout the body, barrel, hips, chest and upper legs likely expressed depending upon the base color and other white variants. RN/n = heterozygous for Roan, white ticking and interspersed white hairs throughout the body, barrel, hips, chest and upper legs likely expressed depending upon the base color and other white variants. n/n = no variant detected Possible combinations: RN1/RN1, RN1/RN2, RN1/RN3, RN2/RN2, RN2/RN3 = homozygous for roan, trait expressed RN1/n, RN2/n, RN3/n = heterozygous for roan, trait expressed
General Description of Roan
The roan coat color is described as the dispersion of white hairs within an otherwise solid color coat. This phenotype is primarily expressed on the body of the horse, including the barrel, hips, chest, shoulders, neck and upper legs with the head and lower legs exhibiting few to no white hairs. Previous research mapped a locus for roan to the KIT region and observed linked markers in a small number of breeds. However, utilizing those linked markers to determine the Roan genotype in other breeds has seen limited success. The roan mutation is dominant, meaning that the coat color of a horse with at least one roan allele is generally observed as a roan and called as such, regardless of the underlying coat color. If the coat color is known, it is identified with “red roan”, “blue roan”, “dun roan” etc.
We have discovered three haplotypes that segregate with a roan haplotype each. Roan 1 (RN1) is present in about 38% of the roan horses studied, and found present in multiple breeds such as American Quarter Horse, American Paint Horse, Noriker Horse, Mustang, Gypsy Horse, Welsh Pony and Cob, Mangalarga Marchador, Percheron, Belgian Draft, European Brabant, Missouri Fox Trotter, and Curly Horse. Within the Quarter Horse breed, we looked at the extended pedigrees of several individuals (Allbreedpedigree.com), and assuming a dominant trait, we found this to be the Roan haplotype traced to the Burnett roan mare (U0069050). One major Quarter Horse sire likely contributing this Roan haplotype to the modern breed is Red Man (née 1935).
Roan 2 (RN2) is present in about 36% of the roan horses studied. This associated haplotype is present in fewer breeds, all based on North American ancestry including the American Quarter Horse, Mustang, Curly Horse, and American Paint Horse (Table 2). Within the American Quarter Horse breed, using the same pedigree analysis as described for Roan 1, we found this to be the Roan haplotype that can be traced to the Burns mare (U0069059) and her offspring Oral’s Kitten. This seems a newer haplotype as it is present only in breeds that originated in the US. It is currently propagated by the influential sires Metallic Cat and Peptoboonsmal.
Just discovered!!!! Roan 3 (RN3) is present in about 15% of horse samples tested. This allele is mostly present in the American Quarter Horse. Using the same pedigree analysis as described for Roan 1, we found this to be the Roan haplotype that can be traced to the Kitch Roan mare (U0073276) and her offspring Margie Star. This seems a newer haplotype as it is present only in breeds that originated in the US. Within the American Quarter Horse it is currently likely propagated by the influential sires Zippos Mr Good Bar, VS Code Blue, and VS Code Red.
The three identified roan alleles account for ~85-90% roan samples tested. Thus there are about 10-15% of roan samples that currently cannot be identified and for which we have seen evidence further alleles may be present, and for which discovery work is in progress. Overall, the RN1 allele was present in 3%, the RN2 allele in 3%, the RN3 allele in 1%, and the unknown allele(s) in 1% of all the horses we have analyzed. So roan is present in about 7% of all horses tested.
We would like to emphasize that these haplotypes are based on association only, they are so-called tag-SNPs, and do not likely include the causal mutation. Tag-SNPs are SNPs that have been found to segregate with the specific trait of interest, in this case roan coat color, but themselves do not cause roan. RN1 to RN3 are indications to discern the origin of the associated haplotypes, and future research will decide whether these are truly different alleles or mere variations of different chromosomal blocks inherited from the roan parent that includes the actual roan causing variant. THey all may lead to the same causal variant. Further research into the genetic basis of the collection of roan phenotypes needs to be performed and is ongoing.
Gene Information
KIT is a tyrosine kinase receptor that is vital for normal development. Mutations in other species have led to white spotting, anemia, sterility, and certain types of tumors. However, no negative health effects associated with roan have been documented to date in the horse. The various KIT alleles and variants encompass a variety of mutations, all resulting in changes to the encoded protein.
References
Roan3: publication in preparation. Coming Soon.
Everts R.E., Caron R., Foster G., Martin K., Brooks S.A., Lafayette C. 2025 Identification of two genetic haplotypes associated with the roan coat color in the American Quarter Horse and other equine breeds. Submitted to Animals.
Marklund S., Moller M.; Sandberg K., Andersson L. Close Association between Sequence Polymorphism in the KIT Gene and the Roan Coat Color in Horses. Mammalian Genome 1999, 10, 283–288, doi:10.1007/S003359900987.
Sponenberg D.P., Harper H.T., Harper A.L. Direct Evidence for Linkage of Roan and Extension Loci in Belgian Horses. J Hered 1984, 75, 413–414, doi:10.1093/OXFORDJOURNALS.JHERED.A109968.
Grilz-Seger G., Reiter S., Neuditschko M., Wallner B., Rieder S., Leeb T., Jagannathan V., Mesarič M., Cotman M., Pausch H., et al. A Genome-Wide Association Analysis in Noriker Horses Identifies a SNP Associated With Roan Coat Color. J Equine Vet Sci 2020, 88, doi:10.1016/J.JEVS.2020.102950.
Voß K., Tetens J., Thaller G., Becker D. Coat Color Roan Shows Association with KIT Variants and No Evidence of Lethality in Icelandic Horses. Genes (Basel) 2020, 11, 680, doi:10.3390/GENES11060680.
More Horse Color Genetics
Congenital Stationary Night Blindness & Leopard Complex
Congential Stationary Night Blindness (CSNB) is characterized by the inability to see well in low light and no-light situations. It is linked to Leopard Complex Spotting (LP), where homozygous horses (LP/LP) will have CSNB. Congential Stationary Night Blindness is present at birth and is non-progressive.
Champagne
Champagne (CH) is a dilution that affects all coat colors. Champagne foals are born with pink skin and blue eyes that slightly darken with age. Adult champagne horses have a distinct pumpkin colored skin with mottling in the hairless regions, as well as amber/green/tan eyes. Horses with multiple dilutions can be difficult to accurately identify color without genetic testing.