Multi-Omics Database of ESCC

ESCCdb: An Integrated Database for Esophageal Squamous Cell Carcinoma

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Consensus DEGs
Recurrent Mutations
Significant CNV
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Somatic mutations of PTGIR:

NM_000960

Mutation details: 11 records

Showing 1-10/11 mutation records.

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E-mail: haoyang.cai@scu.edu.cn
Citation: Jian Yang, et al. Comput Struct Biotechnol J. 2023; 21: 2119–2128.

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College of Life Sciences, Sichuan University, China