This gene is a member of the mitochondrial carrier family which includes nuclear-encoded transporters localized on the inner mitochondrial membranes. Members of the family transport important small molecules across the mitochondrial inner membrane. This protein is involved in the transport of S-adenosylmethionine (SAM) into the mitochondria. Mutations in this gene are associated with combined oxidative phosphorylation deficiency 28. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2017]
Transcription factors with Perturb-seq knockdown data for SLC25A26. 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 = SLC25A26 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 SLC25A26, 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 |
|---|---|---|---|---|
| chr3:65,950,226–65,950,881 | 270.5 kb | Distal (>10kb) Multiome | 135 | |
| chr3:65,953,020–65,953,813 | 267.4 kb | Distal (>10kb) Multiome | 435 | |
| chr3:66,037,331–66,039,992 | 182.0 kb | Distal (>10kb) Multiome | 825 | |
| chr3:66,220,628–66,221,378 | 44 bp | At TSS Multiome | 818 | |
| chr3:66,415,883–66,417,138 | 195.7 kb | Distal (>10kb) Multiome | 115 | |
| chr3:66,441,917–66,443,468 | 221.4 kb | Distal (>10kb) Multiome | 428 | |
| chr3:66,452,752–66,454,355 | 232.9 kb | Distal (>10kb) Multiome | 257 | |
| chr3:66,499,991–66,502,058 | 280.2 kb | Distal (>10kb) Multiome | 746 |
Genomic view of the SLC25A26 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.