Mouse RNA-seq Atlas · Overview

Start with the tissue, then follow the evidence.

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

Mouse evidence at a glance

Counts reflect the current locally generated atlas release.

—curated samples
—independent studies
—genes
9tissue workspaces

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.

How to interpret it

Three complementary views

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

Go directly to the biology.

Every link opens the corresponding analysis within that tissue.

BR

Brain

Brain vascular endothelial cells and matched neurovascular reference populations.

ME

Meninges

Dural lymphatic endothelial cells and meningeal stromal and immune references.

EY

Eye/Retina

Retinal endothelial cells alongside neuronal, glial, immune, photoreceptor, and RPE reference populations.

LU

Lung

Pulmonary endothelial populations compared with epithelial, stromal, and immune cells.

LI

Liver

Sinusoidal endothelial cells in the context of hepatocytes, stellate cells, and liver macrophages.

KI

Kidney

Renal endothelial cells alongside tubular, glomerular, and supporting kidney populations.

HE

Heart

Cardiac endothelial cells alongside cardiomyocytes, fibroblasts, macrophages, and B cells.

BO

Bone/Bone Marrow

Bone and marrow endothelial cells alongside stromal, pericyte, hematopoietic stem/progenitor, neutrophil, and B-cell references. Marrow-derived ECs remain distinct.

GI

GI/Associated Tissues

Intestinal populations, gallbladder tuft cells, and peritoneal macrophages. EC-enrichment and identity calculations retain intestinal tissue references.