PSMD9
proteasome 26S subunit, non-ATPase 9 | Rpn4, p27

The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a non-ATPase subunit of the 19S regulator. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, May 2012]

Member of: DE-1 Developmental clusters: GC6
Biological processes 17 terms
Expression (TPM)
PSMD9 — as a Regulated Gene

TFs regulating PSMD9 0 TFs

Transcription factors with Perturb-seq knockdown data for PSMD9. 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 = PSMD9 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 PSMD9

Open chromatin peaks (ATAC-seq) in the genomic neighbourhood of PSMD9, 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
chr12:121,625,878–121,627,559 262.3 kb Distal (>10kb) Multiome 904
chr12:121,671,731–121,673,334 216.2 kb Distal (>10kb) Multiome 548
chr12:121,686,676–121,687,782 201.7 kb Distal (>10kb) Multiome 907
chr12:121,712,130–121,713,412 176.0 kb Distal (>10kb) Multiome 731
chr12:121,792,642–121,795,650 94.6 kb Distal (>10kb) Multiome HiCAR 1009
chr12:121,797,071–121,801,369 90.2 kb Distal (>10kb) Multiome HiCAR 1126
chr12:121,802,658–121,804,393 85.7 kb Distal (>10kb) Multiome HiCAR 825
chr12:121,812,380–121,813,114 76.3 kb Distal (>10kb) Multiome 458
chr12:121,839,137–121,840,260 49.1 kb Distal (>10kb) Multiome HiCAR 564
chr12:121,888,344–121,889,335 42 bp At TSS Multiome 1141
chr12:121,918,184–121,919,001 29.8 kb Distal (>10kb) Multiome 407
chr12:122,021,348–122,022,698 133.2 kb Distal (>10kb) Multiome 537
chr12:122,063,787–122,064,537 175.4 kb Distal (>10kb) Multiome 742
chr12:122,064,878–122,065,312 176.5 kb Distal (>10kb) Multiome 355
chr12:122,078,081–122,079,394 189.9 kb Distal (>10kb) Multiome 952
chr12:122,097,641–122,098,611 209.3 kb Distal (>10kb) Multiome 462
chr12:122,155,564–122,156,340 267.2 kb Distal (>10kb) Multiome 197
chr12:122,182,856–122,183,527 294.5 kb Distal (>10kb) Multiome 228

Genome Browser

Genomic view of the PSMD9 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.

chr12:121,615,878 – 122,193,527
Proximal 1 kb Distal 10 kb Multiome HiCAR ATAC-seq RNA-seq