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. 2023 May 11;24:192. doi: 10.1186/s12859-023-05323-y

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© The Author(s) 2023

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. 2 — The expression of SYNGR2 in pan-cancer and different pathological stages. A. Differential expression of SYNGR2 in normal and tumor samples of 33 tumors in The Cancer Genome Atlas (TCGA) database. B. Data from TCGA and Genotype-Tissue Expression (GTEx) database showed differential expression of SYNGR2 in multiple cancers. C. Differential expression of SYNGR2 in cancers and normal tissues from TCGA dataset. D. T-SNE plot showing the expression of SYNGR2 in human tissue. E. Expression of SYNGR2 in different pathological stages of indicated tumors. F. SYNGR2 protein expression levels between tumor and respective normal tissues for 8 types of cancers. *p < 0.05, **p < 0.01, and ***p < 0.001