DUSP4
dual specificity phosphatase 4 | HVH2, MKP-2, TYP

The protein encoded by this gene is a member of the dual specificity protein phosphatase subfamily. These phosphatases inactivate their target kinases by dephosphorylating both the phosphoserine/threonine and phosphotyrosine residues. They negatively regulate members of the mitogen-activated protein (MAP) kinase superfamily (MAPK/ERK, SAPK/JNK, p38), which are associated with cellular proliferation and differentiation. Different members of the family of dual specificity phosphatases show distinct substrate specificities for various MAP kinases, different tissue distribution and subcellular localization, and different modes of inducibility of their expression by extracellular stimuli. This gene product inactivates ERK1, ERK2 and JNK, is expressed in a variety of tissues, and is localized in the nucleus. Two alternatively spliced transcript variants, encoding distinct isoforms, have been observed for this gene. In addition, multiple polyadenylation sites have been reported. [provided by RefSeq, Jul 2008]

Member of: DE-4 DE-4.1 Developmental clusters: GC6
Biological processes 22 terms
Expression (TPM)
DUSP4 — as a Regulated Gene

TFs regulating DUSP4 0 TFs

Transcription factors with Perturb-seq knockdown data for DUSP4. 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 = DUSP4 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 DUSP4

Open chromatin peaks (ATAC-seq) in the genomic neighbourhood of DUSP4, 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
chr8:29,146,567–29,147,479 203.7 kb Distal (>10kb) Multiome 158
chr8:29,262,401–29,263,703 87.6 kb Distal (>10kb) Multiome 641
chr8:29,318,868–29,320,832 31.0 kb Distal (>10kb) Multiome 261
chr8:29,340,273–29,340,693 10.0 kb Proximal (<10kb) 341
chr8:29,347,713–29,349,581 1.1 kb Proximal (<10kb) 441
chr8:29,349,763–29,351,657 135 bp At TSS Multiome 719
chr8:29,352,546–29,353,344 1.9 kb Proximal (<10kb) 201
chr8:29,357,919–29,358,285 7.2 kb Proximal (<10kb) 31
chr8:29,408,273–29,408,752 57.9 kb Distal (>10kb) Multiome 166
chr8:29,432,484–29,433,492 82.1 kb Distal (>10kb) Multiome 83
chr8:29,874,798–29,875,362 524.5 kb Distal (>10kb) Multiome HiCAR 162
chr8:29,990,565–29,991,896 640.4 kb Distal (>10kb) Multiome HiCAR 363
chr8:30,005,068–30,006,568 654.8 kb Distal (>10kb) Multiome HiCAR 99
chr8:30,011,371–30,011,980 661.1 kb Distal (>10kb) Multiome HiCAR 36
chr8:30,033,186–30,034,812 683.8 kb Distal (>10kb) Multiome HiCAR 337
chr8:30,034,989–30,035,701 684.9 kb Distal (>10kb) Multiome HiCAR 47

Genome Browser

Genomic view of the DUSP4 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.

chr8:29,136,567 – 30,045,701
Proximal 1 kb Distal 10 kb Multiome HiCAR ATAC-seq RNA-seq