Cytosolic and membrane-bound forms of glutathione S-transferase are encoded by two distinct supergene families. At present, eight distinct classes of the soluble cytoplasmic mammalian glutathione S-transferases have been identified: alpha, kappa, mu, omega, pi, sigma, theta and zeta. This gene encodes a glutathione S-transferase that belongs to the mu class. The mu class of enzymes functions in the detoxification of electrophilic compounds, including carcinogens, therapeutic drugs, environmental toxins and products of oxidative stress, by conjugation with glutathione. The genes encoding the mu class of enzymes are organized in a gene cluster on chromosome 1p13.3 and are known to be highly polymorphic. These genetic variations can change an individual's susceptibility to carcinogens and toxins as well as affect the toxicity and efficacy of certain drugs. Diversification of these genes has occurred in regions encoding substrate-binding domains, as well as in tissue expression patterns, to accommodate an increasing number of foreign compounds. Multiple transcript variants, each encoding a distinct protein isoform, have been identified. [provided by RefSeq, Jul 2008]
Transcription factors with Perturb-seq knockdown data for GSTM4. 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 = GSTM4 upregulated upon KD; negative = downregulated). The Outlier column indicates whether this gene is in the top or bottom 5% of all TF knockdown effects.
| TF | Mean coef | Binding | Outlier | TF→Gene link |
|---|
Open chromatin peaks (ATAC-seq) in the genomic neighbourhood of GSTM4, 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 |
|---|---|---|---|---|
| chr1:109,397,369–109,398,671 | 258.1 kb | Distal (>10kb) Multiome | 654 | |
| chr1:109,425,842–109,427,054 | 229.6 kb | Distal (>10kb) Multiome | 922 | |
| chr1:109,466,294–109,467,385 | 189.5 kb | Distal (>10kb) Multiome | 452 | |
| chr1:109,483,147–109,484,806 | 172.2 kb | Distal (>10kb) Multiome | 1031 | |
| chr1:109,493,695–109,494,597 | 162.0 kb | Distal (>10kb) Multiome | 842 | |
| chr1:109,498,180–109,498,608 | 157.7 kb | Distal (>10kb) Multiome | 178 | |
| chr1:109,509,196–109,510,011 | 146.5 kb | Distal (>10kb) Multiome | 448 | |
| chr1:109,532,157–109,533,159 | 123.4 kb | Distal (>10kb) Multiome | 517 | |
| chr1:109,548,385–109,549,096 | 107.5 kb | Distal (>10kb) Multiome | 855 | |
| chr1:109,619,434–109,621,357 | 35.1 kb | Distal (>10kb) Multiome | 814 | |
| chr1:109,643,342–109,643,856 | 12.6 kb | Distal (>10kb) Multiome | 470 | |
| chr1:109,655,698–109,656,566 | 33 bp | At TSS Multiome | 707 | |
| chr1:109,667,812–109,668,362 | 11.9 kb | Distal (>10kb) Multiome | 287 | |
| chr1:109,739,695–109,740,873 | 84.1 kb | Distal (>10kb) Multiome | 633 | |
| chr1:109,877,325–109,877,790 | 221.4 kb | Distal (>10kb) Multiome | 378 | |
| chr1:109,910,465–109,911,472 | 254.7 kb | Distal (>10kb) Multiome | 618 | |
| chr1:109,931,127–109,931,638 | 275.2 kb | Distal (>10kb) Multiome | 379 | |
| chr1:109,984,134–109,985,352 | 328.6 kb | Distal (>10kb) Multiome HiCAR | 946 |
Genomic view of the GSTM4 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.