MIR92A1
microRNA 92a-1 | hsa-mir-92-1, hsa-mir-92a-1, MIRN92-1, MIRN92A1

microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]

Biological processes 44 terms
RISC complex (GO:0016442)blood vessel diameter maintenance (GO:0097746)cellular response to fatty acid (GO:0071398)cellular response to low-density lipoprotein particle stimulus (GO:0071404)cellular stress response to acid chemical (GO:0097533)cytoplasm (GO:0005737)extracellular region (GO:0005576)extracellular vesicle (GO:1903561)mRNA 3'-UTR binding (GO:0003730)mRNA base-pairing post-transcriptional repressor activity (GO:1903231)mRNA base-pairing post-transcriptional repressor activity (GO:1903231)miRNA-mediated gene silencing by inhibition of translation (GO:0035278)miRNA-mediated post-transcriptional gene silencing (GO:0035195)miRNA-mediated post-transcriptional gene silencing (GO:0035195)miRNA-mediated post-transcriptional gene silencing (GO:0035195)negative regulation of JNK cascade (GO:0046329)negative regulation of angiogenesis (GO:0016525)negative regulation of blood vessel endothelial cell migration (GO:0043537)negative regulation of collagen biosynthetic process (GO:0032966)negative regulation of endothelial cell proliferation (GO:0001937)negative regulation of endothelial cell-matrix adhesion (GO:1904905)negative regulation of extracellular matrix disassembly (GO:0010716)negative regulation of gene expression (GO:0010629)negative regulation of inflammatory response (GO:0050728)negative regulation of intrinsic apoptotic signaling pathway in response to hydrogen peroxide (GO:1903751)negative regulation of nitric oxide biosynthetic process (GO:0045019)negative regulation of smooth muscle cell apoptotic process (GO:0034392)negative regulation of sprouting angiogenesis (GO:1903671)positive regulation of JNK cascade (GO:0046330)positive regulation of acute inflammatory response (GO:0002675)positive regulation of apoptotic process (GO:0043065)positive regulation of endothelial cell activation (GO:1904989)positive regulation of gene expression (GO:0010628)positive regulation of gene expression (GO:0010628)positive regulation of inflammatory response (GO:0050729)positive regulation of interleukin-6 production (GO:0032755)positive regulation of leukocyte adhesion to arterial endothelial cell (GO:1904999)positive regulation of leukocyte adhesion to vascular endothelial cell (GO:1904996)positive regulation of leukocyte adhesion to vascular endothelial cell (GO:1904996)positive regulation of monocyte chemotactic protein-1 production (GO:0071639)positive regulation of programmed necrotic cell death (GO:0062100)positive regulation of sprouting angiogenesis (GO:1903672)regulation of heart contraction (GO:0008016)vascular endothelial cell response to fluid shear stress (GO:0097699)
Expression (TPM)
MIR92A1 — as a Regulated Gene

TFs regulating MIR92A1 0 TFs

Transcription factors with Perturb-seq knockdown data for MIR92A1. The Binding column indicates whether any binding evidence exists for this TF–gene pair (ChIP-seq or motif footprint peaks). The Mean coef is the average Perturb-seq regression coefficient across active gRNAs (positive = MIR92A1 upregulated upon KD; negative = downregulated). The Outlier column indicates whether this gene is in the top or bottom 5% of all TF knockdown effects.

Data: Effect:
TF Mean coef Binding Outlier TF→Gene link

Elements linked to MIR92A1

Open chromatin peaks (ATAC-seq) in the genomic neighbourhood of MIR92A1, linked by TSS proximity or chromatin conformation (Multiome / HiCAR). Each element overlaps at least one TF ChIP-seq binding site — the TFs column shows how many distinct TFs bind that element.

Accessibility Element Dist. to TSS Link type TFs
chr13:91,346,886–91,349,419 1.9 kb Proximal (<10kb) 1086
chr13:91,355,494–91,355,685 4.2 kb Proximal (<10kb) 77
chr13:91,355,942–91,356,646 4.6 kb Proximal (<10kb) 91
chr13:91,356,761–91,357,559 5.4 kb Proximal (<10kb) 192
chr13:91,357,725–91,358,747 6.4 kb Proximal (<10kb) 170
chr13:91,358,859–91,359,737 7.5 kb Proximal (<10kb) 100
chr13:91,360,228–91,361,348 8.9 kb Proximal (<10kb) 90

Genome Browser

Genomic view of the MIR92A1 locus showing ATAC-seq accessibility and RNA-seq expression across the ESC → DE time course, together with TF binding peaks and element-to-TSS loop connections.

chr13:91,336,886 – 91,371,348
Proximal 1 kb Distal 10 kb Multiome HiCAR ATAC-seq RNA-seq