SCREATE

Cell state · L2

EC.venous.cardiac_structural

779 cells in the full atlas (not the displayed sample).

These are the cell-population annotations shown in the SCREATE Cell Browser.

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Marker genes

ANKRD36, CREBZF, EPB41L2, HIF3A, NPIPB13, NPIPB5, PRICKLE4, PTPN5, STX16, SYNE1, TNNC1, TPO, XIST

Annotation genes

CREBZF, EPB41L2, STX16, SYNE1

Annotation rationales

SYNE1 anchors the nucleus to cytoskeleton (LINC complex) for mechano-transduction; EPB41L2 supports membrane–cytoskeletal stability. STX16 enables vesicle trafficking, and HIF3A tunes responses to fluctuating oxygen in myocardium. This reflects venous ECs adapting to cyclic strain and variable oxygen in the heart.

Functional implications

Mechanics-adapted venous ECs that withstand cyclic stretch and shear gradients in cardiac venules. They maintain vesicular transport, junctional integrity, and oxygen sensing without overt inflammation, ensuring venous return from myocardium while preventing barrier breakdown under repetitive cardiac load.

Marker and functional descriptions are atlas annotations. Explore gene expression, trait associations and regulatory elements in the interactive browsers; see the browser guide.