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. 2018 Feb 28;9:859. doi: 10.1038/s41467-017-02809-1

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© The Author(s) 2018

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 5 — Candidate causal missense mutation in FBXL3. a FBXL3 gene representation in human hg19 coordinates chr13:77579389-77601337. b Multiple sequence alignment of SNP across representative vertebrates. c Allele frequency of the G (reference) or A (alternative) allele in domestic sheep (O. aries) (n = 67) or mouflon (O. orientalis) (n = 17). d FBXL3 amino acid sequence with the substitution at residue 182 highlighted in red. Residue 358 (green) is associated with the mouse After hour (Afh) phenotype residue 364 with the overtime phenotype (Ovt)