PCSK7
proprotein convertase subtilisin/kexin type 7 | LPC, PC7, PC8, SPC7

This gene encodes a member of the subtilisin-like proprotein convertase family, which includes proteases that process protein and peptide precursors trafficking through regulated or constitutive branches of the secretory pathway. It encodes a type 1 membrane bound protease that is expressed in many tissues, including neuroendocrine, liver, gut, and brain. The encoded protein undergoes an initial autocatalytic processing event in the ER and then sorts to the trans-Golgi network through endosomes where a second autocatalytic event takes place and the catalytic activity is acquired. This gene encodes one of the seven basic amino acid-specific members which cleave their substrates at single or paired basic residues. It can process proalbumin and is thought to be responsible for the activation of HIV envelope glycoproteins gp160 and gp140. This gene has been implicated in the transcriptional regulation of housekeeping genes and plays a role in the regulation of iron metabolism. A t(11;14)(q23;q32) chromosome translocation associated with B-cell lymphoma occurs between this gene and its inverted counterpart. [provided by RefSeq, Feb 2014]

Member of: DE-4 DE-4.19 Developmental clusters: GC2
Biological processes 17 terms
Expression (TPM)
PCSK7 — as a Regulated Gene

TFs regulating PCSK7 0 TFs

Transcription factors with Perturb-seq knockdown data for PCSK7. 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 = PCSK7 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 PCSK7

Open chromatin peaks (ATAC-seq) in the genomic neighbourhood of PCSK7, 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
chr11:117,097,570–117,099,243 133.6 kb Distal (>10kb) Multiome 739
chr11:117,099,458–117,100,103 132.1 kb Distal (>10kb) Multiome 62
chr11:117,143,916–117,144,864 87.7 kb Distal (>10kb) Multiome 969
chr11:117,178,198–117,179,718 53.3 kb Distal (>10kb) Multiome 726
chr11:117,197,957–117,198,434 34.0 kb Distal (>10kb) Multiome 160
chr11:117,198,962–117,199,797 32.8 kb Distal (>10kb) Multiome 211
chr11:117,226,522–117,226,719 5.4 kb Proximal (<10kb) 133
chr11:117,231,703–117,233,431 467 bp At TSS Multiome 703
chr11:117,315,726–117,316,638 84.2 kb Distal (>10kb) Multiome 619
chr11:117,327,486–117,328,627 95.8 kb Distal (>10kb) Multiome 751
chr11:117,410,817–117,412,004 179.3 kb Distal (>10kb) Multiome 247
chr11:117,429,727–117,430,361 198.0 kb Distal (>10kb) Multiome 126
chr11:117,443,412–117,443,876 211.7 kb Distal (>10kb) Multiome 185

Genome Browser

Genomic view of the PCSK7 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.

chr11:117,087,570 – 117,453,876
Proximal 1 kb Distal 10 kb Multiome HiCAR ATAC-seq RNA-seq