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. 2020 Jul 23;21:81. doi: 10.1186/s12863-020-00888-6

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© The Author(s) 2020

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 7 — Phenotypic analyses of C3H, C3H-Chr 11^NSY, and four congenic strains (R1, R2, R3, and R4). Mice were administered 30% (w/v) sucrose solution from 4 weeks of age, and the phenotypes were studied at 15 weeks of age. a Body weight. b White adipose tissue weight percentages (sum of epididymal fat, retroperitoneal fat, and mesenteric fat). c Liver weight percentages. (C3H, n = 6; C3H-Chr 11^NSY, n = 4; R1, n = 6; R2, n = 7; R3, n = 8; R4, n = 5). ^a,b,c,d Means without common letters are significantly different by Tukey test (P < 0.05)