SCUBA

HEY1 — Hes related family bHLH transcription factor with YRPW motif 1

HEY1 belongs to a gene co-expression module in 3 of 28 SCUBA cell types. Each module groups genes that rise and fall together in that cell type; the genes it shares a module with are its closest co-expression partners there.

HEY1's module in each cell type

Cell typeModuleShares the module with
EndothelialNotch Arterial Identity
Endothelial cell development
ADAMTS1, ARID5A, BTG1, BTG2, CRIP1, DLL4, EFNA1, EFNB2 +14 moreView in SCUBA
Lymphatic endothelialNotch TGF-β Endothelial
endothelial development
ARF6, ARL4C, C16orf87, CCNL1, CLK1, DEDD2, ELOC, GPBP1 +11 moreView in SCUBA
PericytesArterial Notch Signaling
Developmental
BCL6B, CYTH1, DLL4, EFNB2, MSX1, NEDD9, PNP, SGK1 +1 moreView in SCUBA

About the gene

SynonymsbHLHb31, CHF-2, CHF2, HERP2, HESR-1, HESR1, HRT-1
Chromosome8: 79762371-79767857
Predicted locationIntracellular
Essential geneNo
Protein classCancer-related genes, Predicted intracellular proteins, Transcription factors, Transporters
Molecular functionDevelopmental protein, DNA-binding, Repressor
Biological processNotch signaling pathway, Transcription, Transcription regulation

Function

Transcriptional repressor which binds preferentially to the canonical E box sequence 5'-CACGTG-3'. Downstream effector of Notch signaling required for cardiovascular development. Specifically required for the Notch-induced endocardial epithelial to mesenchymal transition, which is itself criticial for cardiac valve and septum development. May be required in conjunction with HEY2 to specify arterial cell fate or identity. Promotes maintenance of neuronal precursor cells and glial versus neuronal fate specification. Represses transcription by the cardiac transcriptional activators GATA4 and GATA6 and by the neuronal bHLH factors ASCL1/MASH1 and NEUROD4/MATH3. Involved in the regulation of liver cancer cells self-renewal.

Human Protein Atlas · Open Targets · UniProt

Gene annotation from the Human Protein Atlas and UniProt; see sources & licences.