CHURC1-FNTB
CHURC1-FNTB readthrough

This locus represents naturally occurring read-through transcription between the neighboring CHURC1 (churchill domain containing 1) and FNTB (farnesyltransferase, CAAX box, beta) on chromosome 14. The read-through transcript produces a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, Feb 2011]

Developmental clusters: GC5
Expression (TPM)
CHURC1-FNTB — as a Regulated Gene

TFs regulating CHURC1-FNTB 0 TFs

Transcription factors with Perturb-seq knockdown data for CHURC1-FNTB. 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 = CHURC1-FNTB 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 CHURC1-FNTB

Open chromatin peaks (ATAC-seq) in the genomic neighbourhood of CHURC1-FNTB, 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
chr14:64,914,197–64,914,885 at TSS At TSS 741

Genome Browser

Genomic view of the CHURC1-FNTB 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.

chr14:64,904,197 – 64,924,885
Proximal 1 kb Distal 10 kb Multiome HiCAR ATAC-seq RNA-seq