NDRG1
N-myc downstream regulated 1 | DRG1, NDR1, RTP, TDD5, CAP43

This gene is a member of the N-myc downregulated gene family which belongs to the alpha/beta hydrolase superfamily. The protein encoded by this gene is a cytoplasmic protein involved in stress responses, hormone responses, cell growth, and differentiation. The encoded protein is necessary for p53-mediated caspase activation and apoptosis. Mutations in this gene are a cause of Charcot-Marie-Tooth disease type 4D, and expression of this gene may be a prognostic indicator for several types of cancer. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, May 2012]

Developmental clusters: GC6
Biological processes 31 terms
Expression (TPM)
NDRG1 — as a Regulated Gene

TFs regulating NDRG1 0 TFs

Transcription factors with Perturb-seq knockdown data for NDRG1. 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 = NDRG1 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 NDRG1

Open chromatin peaks (ATAC-seq) in the genomic neighbourhood of NDRG1, 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
chr8:133,295,154–133,295,609 1.6 kb Proximal (<10kb) 127
chr8:133,295,722–133,298,151 at TSS At TSS 1077

Genome Browser

Genomic view of the NDRG1 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.

chr8:133,285,154 – 133,308,151
Proximal 1 kb Distal 10 kb Multiome HiCAR ATAC-seq RNA-seq