Additional file 2 of Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes
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https://springernature.figshare.com/articles/dataset/Additional_file_2_of_Integration_of_genetic_transcriptomic_and_clinical_data_provides_insight_into_16p11_2_and_22q11_2_CNV_genes/16907197/1
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Additional file 2: Table S2. List of genes at or near 16p11.2 and 22q11.2. List of coding and non-coding genes in the CNV region, as well as flanking genes 200 kb on either side. Genes for which PrediXcan models based on GTEx v7 were available and the range of model qualities (R2) are noted, along with the number of tissues in which prediction models were available. Genes are annotated with their type (e.g., protein-coding, pseudogene, etc.), whether they are in the CNV or flanking, and any other names by which they may be referred in the literature.
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figshare
创建时间：
2021-10-30
