Hepatocyte nuclear factor 1β binding in E14.5 kidney
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE205189
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资源简介：
HNF-1β mutations are one of the most common single-gene mutations that underlie kidney developmental disease. Hepatocyte nuclear factor 1β (HNF-1β) is essential for kidney development, but its functions in kidney development are incompletely understood. We identified 8284 HNF-1β binding sites using ChIP-sequencing. The majority of these peaks map to promoter (26%), intron (34%) or distal intergenic regions (37.4%) of the mouse genome. 61% of peaks map to protein coding genes, 12% map to long-noncoding RNAs, and 2% map to miRNAs. Chromatin immunoprecipitation DNA-sequencing (ChIP-seq) for HNF-1β in embryonic day 14.5 mouse kidneys
创建时间：
2022-10-28
