What this page accomplishes
A map into the atlas
Choose the biological tissue first. Each primary tissue workspace follows the same analysis sequence so results remain comparable without losing tissue context.
Mouse RNA-seq Atlas · Overview
This atlas harmonizes curated control bulk RNA-seq studies so endothelial identity can be compared across tissues, studies, and matched reference cell types.
Atlas snapshot
Counts reflect the current locally generated atlas release.
What this page accomplishes
Choose the biological tissue first. Each primary tissue workspace follows the same analysis sequence so results remain comparable without losing tissue context.
How to interpret it
PCA and UMAP show sample-level structure. EC-Enriched Genes tests endothelial-versus-reference evidence. Identity & Composition groups reference context with vascular expression programs as supporting atlas information.
Tissue workspaces
Every link opens the corresponding analysis within that tissue.
Brain vascular endothelial cells and matched neurovascular reference populations.
Dural lymphatic endothelial cells and meningeal stromal and immune references.
Retinal endothelial cells alongside neuronal, glial, immune, photoreceptor, and RPE reference populations.
Pulmonary endothelial populations compared with epithelial, stromal, and immune cells.
Sinusoidal endothelial cells in the context of hepatocytes, stellate cells, and liver macrophages.
Renal endothelial cells alongside tubular, glomerular, and supporting kidney populations.
Cardiac endothelial cells alongside cardiomyocytes, fibroblasts, macrophages, and B cells.
Bone and marrow endothelial cells alongside stromal, pericyte, hematopoietic stem/progenitor, neutrophil, and B-cell references. Marrow-derived ECs remain distinct.
Intestinal populations, gallbladder tuft cells, and peritoneal macrophages. EC-enrichment and identity calculations retain intestinal tissue references.