Genetic Polymorphisms of Candidate Loci and Inheritance Ppatterns of Gray Coat Color in Jeju Horses.
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Han, Sang-Hyun
(Jeju-Substation, National Institute of Animal Science)
Lee, Chong-Eon (Jeju-Substation, National Institute of Animal Science) Kim, Nam-Young (Jeju-Substation, National Institute of Animal Science) Ko, Moon-Suck (Jeju-Substation, National Institute of Animal Science) Jeong, Ha-Yeon (Jeju-Substation, National Institute of Animal Science) Lee, Sung-Soo (Jeju-Substation, National Institute of Animal Science) |
1 | Sambrook, J., E. F. Fritsch, and T. Manniatis. 1989. Molecular cloning: a laboratory mannual. 2nd Ed. Cold Spring Harbor Laboratory |
2 | Santschi E. M., A. K. Purdy, S. J. Valberg, P. D. Vrotsos, H. Kaese, and J. R. Mickelson. 1998. Endothelin receptor B polymorphism associated with lethal white foal syndrome in horses. Mamm. Genome 9, 306-309 DOI ScienceOn |
3 | Schmutz, S. M., T. G. Berryere, D. C. Ciobanu, A. J. Mileham, B. H. Schmidtz, and M. Fredholm. 2004. A form of albinism in cattle is caused by a tyrosinase frameshift mutation. Mamm. Genome 15, 62-67 DOI ScienceOn |
4 | Sponenberg, D. P. 2003. Equine Coat Color Genetics. Blackwell. Ames, U.S.A |
5 | Swinburne, J. E., A. Hopkins, and M. M. Binns. 2002. Assignment of the horse grey coat color gene to ECA25 using whole genome scanning. Anim. Genet. 33, 338-342 DOI ScienceOn |
6 | Shutton, R. H. and G. T. Coleman. 1997. Melanoma and graying horse (RIRDC Research Paper Series). pp. 1-34. Barton, Australia |
7 | Yang, G. C., D. Croaker, A. L. Zhang, P. Manglick, T. Cartmill, and D. Cass. 1998. A dinucleotide mutation in the endothelin-B receptor gene is associated with lethal white foal syndrome (LWFS); a horse variant of Hirschsprung disease (HSCR). Hum. Mol. Genet. 7, 1047-1052 DOI ScienceOn |
8 | Zhao, Z. Z., D. L. Duffy, S. A. Thomas, N. G. Martin, N. K. Hayward, and G. W. Montgomery. 2009. Polymorphisms in the syntaxin 17 gene are not associated with human cutaneous malignant melanoma. Melanoma Res. [Epub ahead of print] |
9 | Marklund, L., M. J. Moller, K. Sandberg, and L. Andersson. 1996. A missense mutation in the gene for melanocyte-stimulating hormone receptor (MC1R) is associated with the chestnut coat color in horses. Mamm. Genome 7, 895-899 DOI ScienceOn |
10 | Marklund, S., M. J. Moller, K. Sandberg, and L. Andersson. 1999. Close association between sequence polymorphism in the KIT gene and the roan coat color in horses. Mamm. Genome 10, 283-288 DOI ScienceOn |
11 | Metallinos, D. L., A. T. Bowling, and J. Rine. 1998. A missense mutation in the endothelin-B receptor gene is associated with Lethal White Foal Syndrome: an equine version of Hirschsprung Disease. Mamm. Genome 9, 426-431 DOI ScienceOn |
12 | Pielberg, R. G., A. Golovko, E. Sundstrom, I. Curik, J. Lennartsson, M. H. Seltenhammer, T. Druml, M. Binns, C. Fitzsimmons, G. Lindgren, K. Sandberg, R. Baumung, M. Vetterlein, S. Stromberg, M. Grabherr, C. Wade, K. Lindblad-Toh, F. Ponten, C. H. Heldin, J. Solkner, and L. Andersson. 2008. A cis-acting regulatory mutation causes premature hair graying and susceptibility to melanoma in the horse. Nat. Genet. 40, 1004-1009 DOI ScienceOn |
13 | Pielberg, G., S. Mikko, K. Sandberg, and L. Andersson. 2005. Comparative linkage mapping of the grey coat colour gene in horses. Anim. Genet. 36, 390-395 DOI ScienceOn |
14 | Polus, W. L. and F. B. Hutt. 1969. Lethal dominant white in horses. J. Hered. 60, 59-63 |
15 | Oetting, W. S. and R. A. King. 1999. Molecular basis of albinism: mutations and polymorphisms of pigmentation genes associated with albinism. Hum. Mutat. 13, 99-115 DOI ScienceOn |
16 | Rieder, S., S. Taourit, D. Mariat, B. Langlois, and G. Guerin. 2001. Mutations in the agouti (ASIP), the extension (MC1R), and the brown (TYRP1) loci and their association to coat color phenotypes in horses (Equus caballus). Mamm. Genome 12, 450-455 DOI ScienceOn |
17 | Gronskov, K., J. Ek, and K. Brondum-Nielsen. 2007. Oculocutaneous albinism. Orphanet. J. Rare Dis. 2, 43 DOI ScienceOn |
18 | Blaszczyk, W. M., L. Arning, K. P. Hoffmann, and J. T. Epplen. 2005. A Tyrosinase missense mutation causes albinism in the Wistar rat. Pigment Cell Res. 18, 144-145 DOI ScienceOn |
19 | Blaszczyk, W. M., C. Distler, G. Dekomien, L. Arning, K. P. Hoffmann, and J. T. Epplen. 2007. Identification of a tyrosinase (TYR) exon 4 deletion in albino ferrets (Mustela putorius furo). Anim. Genet. 38, 421-423 DOI ScienceOn |
20 | Giebel, L. B., M. A. Musarella, and R. A. Spritz. 1991. A nonsense mutation in the tyrosinase gene of Afghan patients with tyrosinase negative (type IA) oculocutaneous albinism. J. Med. Genet. 28, 464-467 DOI |
21 | Haase, B., S. A. Brooks, A., Schlumbaum, P. J. Azor, E. Bailey, F. Alaeddine, M. Mevissen, D. Burger, P. A. Poncet, S. Rieder, and T. Leeb. 2007. Allelic heterogeneity at the equine KIT locus in dominant white (W) horses. PLoS Genet. 3, e195 DOI ScienceOn |
22 | Imes, D. L., L. A. Geary, R. A. Grahn, and L. A. Lyons. 2006. Albinism in the domestic cat (Felis catus) is associated with a tyrosinase (TYR) mutation. Anim. Genet. 37, 175-178 DOI ScienceOn |
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