SCUBA

RUNX1 — RUNX family transcription factor 1

RUNX1 belongs to a gene co-expression module in 7 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.

RUNX1's module in each cell type

Cell typeModuleShares the module with
CD4⁺ T cellsRho-GTPase Migration
migration & adhesion
ARHGAP18, ARHGEF7, FNBP1, HELZ, LPXN, MAP4K1, MIS18BP1, PREX1 +4 moreView in SCUBA
FibroblastsInflammatory Fibroblast Activation
Inflammatory
ATP2A2, BAMBI, C5AR2, CRISPLD2, CSNK1E, CTNNB1, DLC1, ETS2 +11 moreView in SCUBA
MacrophagesAlternative Activation Lipid
Lipid metabolism
ACSL1, ADCY3, AGFG1, ARHGEF10L, ARID5B, ATP2B4, BCL6, CCL13 +24 moreView in SCUBA
MonocytesHypoxia Response
Tissue adaptation
ANPEP, ELL2, GNA15, HIF1A, NDRG1, SDC4, SLC7A5, SPAG9 +2 moreView in SCUBA
Mucosal-associated invariant T cellChromatin Remodeling
DNA/chromatin regulation
ANK3, ARHGAP15, ARL15, BCAS3, CAMKMT, CCDC91, DPYD, EDA +13 more
NeutrophilsGranulopoiesis Program
Developmental
ARHGAP24, ARID1B, B4GALT5, CSGALNACT1, FLI1, IQGAP2, LYST, PDZD8 +5 more
PericytesPericyte Inflammatory Activation
Inflammatory
BATF3, CRISPLD2, FILIP1L, KCNJ8, MARCKS, PAG1, PDGFA, RHOBTB3 +3 moreView in SCUBA

About the gene

SynonymsAML1, AMLCR1, CBFA2, PEBP2A2
Chromosome21: 34787801-36004667
Predicted locationIntracellular
Essential geneNo
Protein classCancer-related genes, Disease related genes, Human disease related genes, Plasma proteins, Predicted intracellular proteins, Transcription factors
Molecular functionActivator, DNA-binding, Repressor
Biological processTranscription, Transcription regulation

Function

Forms the heterodimeric complex core-binding factor (CBF) with CBFB. RUNX members modulate the transcription of their target genes through recognizing the core consensus binding sequence 5'- TGTGGT-3', or very rarely, 5'-TGCGGT-3', within their regulatory regions via their runt domain, while CBFB is a non-DNA-binding regulatory subunit that allosterically enhances the sequence-specific DNA-binding capacity of RUNX. The heterodimers bind to the core site of a number of enhancers and promoters, including murine leukemia virus, polyomavirus enhancer, T-cell receptor enhancers, LCK, IL3 and GM-CSF promoters (Probable). Essential for the development of normal hematopoiesis. Acts synergistically with ELF4 to transactivate the IL-3 promoter and with ELF2 to transactivate the BLK promoter. Inhibits KAT6B-dependent transcriptional activation (By similarity). Involved in lineage commitment of immature T cell precursors. CBF complexes repress ZBTB7B transcription factor during cytotoxic (CD8+) T cell development. They bind to RUNX-binding sequence within the ZBTB7B locus acting as transcriptional silencer and allowing for cytotoxic T cell differentiation. CBF complexes binding to the transcriptional silencer is essential for recruitment of nuclear protein complexes that catalyze epigenetic modifications to establish epigenetic ZBTB7B silencing (By similarity). Controls the anergy and suppressive function of regulatory T-cells (Treg) by associating with FOXP3. Activates the expression of IL2 and IFNG and down-regulates the expression of TNFRSF18, IL2RA and CTLA4, in conventional T-cells. Positively regulates the expression of RORC in T-helper 17 cells (By similarity). Isoform AML-1G shows higher binding activities for target genes and binds TCR-beta-E2 and RAG-1 target site with threefold higher affinity than other isoforms. It is less effective in the context of neutrophil terminal differentiation. Isoform AML-1L interferes with the transactivation activity of RUNX1

Human Protein Atlas · Open Targets · UniProt

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