Variant in theRFWD3gene associated withPATN1, a modifier of leopard complex spotting-Reference-Cited by-同舟云学术

Variant in theRFWD3gene associated withPATN1, a modifier of leopard complex spotting

Published:2015-11-16 Issue:1 Volume:47 Page:91-101
ISSN:0268-9146
Container-title:Animal Genetics
language:en
Short-container-title:Anim Genet

Author:

Holl H. M.¹,Brooks S. A.¹,Archer S.²,Brown K.³,Malvick J.⁴,Penedo M. C. T.⁴,Bellone R. R.⁵

Affiliation:

1. Department of Animal Science; Cornell University; Ithaca NY 14853 USA

2. Quill Lake SK S0A3E0 Canada

3. Department of Biology; University of Tampa; Tampa FL 33606 USA

4. Veterinary Genetics Laboratory; School of Veterinary Medicine; University of California-Davis; Davis CA 95616 USA

5. Department of Population Health and Reproduction; Veterinary Genetics Laboratory; School of Veterinary Medicine; University of California-Davis; Davis CA 95616 USA

Funder

Appaloosa Horse Club of Canada

Appaloosa

University of Tampa

Publisher

Wiley

Subject

Genetics,Animal Science and Zoology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/age.12375/fullpdf

Reference50 articles.

1. haploview: analysis and visualization of LD and haplotype maps;Barrett;Bioinformatics,2005

2. Differential gene expression of TRPM1, the potential cause of congenital stationary night blindness and coat spotting patterns (LP) in the Appaloosa horse (Equus caballus);Bellone;Genetics,2008

3. Evidence for a retroviral insertion in TRPM1 as the cause of congenital stationary night blindness and leopard complex spotting in the horse;Bellone;PLoS ONE,2013

4. Exon skipping in the KIT gene causes a sabino spotting pattern in horses;Brooks;Mammalian Genome,2005

5. A chromosome inversion near the KIT gene and the tobiano spotting pattern in horses;Brooks;Cytogenetic and Genome Research,2007

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