SMCR2
Smith-Magenis syndrome chromosome region, candidate 2
Expression (TPM)
SMCR2 — as a Regulated Gene

TFs regulating SMCR2 0 TFs

Transcription factors with Perturb-seq knockdown data for SMCR2. 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 = SMCR2 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 SMCR2

Open chromatin peaks (ATAC-seq) in the genomic neighbourhood of SMCR2, 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
chr17:17,680,744–17,682,037 3.1 kb Proximal (<10kb) 507
chr17:17,682,791–17,683,426 5.1 kb Proximal (<10kb) 510

Genome Browser

Genomic view of the SMCR2 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.

chr17:17,670,744 – 17,693,426
Proximal 1 kb Distal 10 kb Multiome HiCAR ATAC-seq RNA-seq