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. 2021 Jun 1;11:11461. doi: 10.1038/s41598-021-90685-7

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© The Author(s) 2021

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 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/.

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Differential gene expression (Log₂ fold change) data of 36 RING finger protein genes in three genotypes ‘TAC 75’, ‘TAC 6’ and parent ‘C 306’ at four seed developmental stages (7, 14, 21, and 28 DAA (days after anthesis) using qRT-PCR analysis. Differential gene expression analysis was performed in two groups; (A) Group 1 (‘TAC 75’ vs. ‘C 306) and (B) Group 2 (‘TAC 6’ vs. ‘C 306’). ‘TAC 75’ and ‘TAC 6’ are high and low amylose mutant lines derived from parent variety ‘C 306’ with amylose percent ~ 65%, ~ 7%, ~ 26%, respectively. The 11 candidate RING protein genes are marked with red color (down-regulated in high amylose line) and blue color (up-regulated in high amylose line).