CHKB-CPT1B
CHKB-CPT1B readthrough (NMD candidate)

The genes CHKB and CPT1B are adjacent on chromosome 22 and read-through transcripts are expressed that include exons from both loci. The read-through transcripts are candidates for nonsense-mediated mRNA decay (NMD) and are unlikely to express proteins. [provided by RefSeq, Jun 2009]

Expression (TPM)
CHKB-CPT1B — as a Regulated Gene

TFs regulating CHKB-CPT1B 0 TFs

Transcription factors with Perturb-seq knockdown data for CHKB-CPT1B. 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 = CHKB-CPT1B 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 CHKB-CPT1B

Open chromatin peaks (ATAC-seq) in the genomic neighbourhood of CHKB-CPT1B, 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
chr22:50,582,134–50,583,431 at TSS At TSS 871

Genome Browser

Genomic view of the CHKB-CPT1B 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.

chr22:50,572,134 – 50,593,431
Proximal 1 kb Distal 10 kb Multiome HiCAR ATAC-seq RNA-seq