MIR138-1
microRNA 138-1 | hsa-mir-138-1, MIRN138-1

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 28 terms
RISC complex (GO:0016442)cytoplasm (GO:0005737)mRNA 3'-UTR binding (GO:0003730)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)negative regulation of ERK1 and ERK2 cascade (GO:0070373)negative regulation of adipose tissue development (GO:1904178)negative regulation of canonical NF-kappaB signal transduction (GO:0043124)negative regulation of cell adhesion (GO:0007162)negative regulation of cell migration (GO:0030336)negative regulation of cell population proliferation (GO:0008285)negative regulation of fat cell differentiation (GO:0045599)negative regulation of inflammatory response (GO:0050728)negative regulation of intracellular signal transduction (GO:1902532)negative regulation of lipid storage (GO:0010888)negative regulation of osteoblast differentiation (GO:0045668)negative regulation of osteoblast differentiation (GO:0045668)negative regulation of osteoblast proliferation (GO:0033689)negative regulation of protein K63-linked ubiquitination (GO:1900045)negative regulation of response to cytokine stimulus (GO:0060761)negative regulation of sprouting angiogenesis (GO:1903671)negative regulation of stress fiber assembly (GO:0051497)negative regulation of vascular associated smooth muscle cell apoptotic process (GO:1905460)plasma membrane raft assembly (GO:0044854)positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction (GO:0051897)vasodilation (GO:0042311)
Expression (TPM)
MIR138-1 — as a Regulated Gene

TFs regulating MIR138-1 0 TFs

Transcription factors with Perturb-seq knockdown data for MIR138-1. 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 = MIR138-1 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 MIR138-1

Open chromatin peaks (ATAC-seq) in the genomic neighbourhood of MIR138-1, 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
chr3:44,114,176–44,114,444 at TSS At TSS 121

Genome Browser

Genomic view of the MIR138-1 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.

chr3:44,104,176 – 44,124,444
Proximal 1 kb Distal 10 kb Multiome HiCAR ATAC-seq RNA-seq