This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. Mutations in this gene were found in patients with isolated deficiency of pituitary POMC-derived ACTH, suggesting an essential role for this gene in differentiation of the pituitary POMC lineage. ACTH deficiency is characterized by adrenal insufficiency symptoms such as weight loss, lack of appetite (anorexia), weakness, nausea, vomiting, and low blood pressure. [provided by RefSeq, Jul 2008]
Transcription factors with Perturb-seq knockdown data for TBX19. 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 = TBX19 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 TBX19, 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 |
|---|---|---|---|---|
| chr1:168,082,150–168,082,782 | 208.7 kb | Distal (>10kb) Multiome | 282 | |
| chr1:168,135,686–168,137,665 | 154.3 kb | Distal (>10kb) Multiome | 557 | |
| chr1:168,145,525–168,146,368 | 145.2 kb | Distal (>10kb) Multiome | 327 | |
| chr1:168,146,489–168,147,203 | 144.3 kb | Distal (>10kb) Multiome | 155 | |
| chr1:168,178,414–168,179,583 | 112.3 kb | Distal (>10kb) Multiome | 940 | |
| chr1:168,187,044–168,187,988 | 103.7 kb | Distal (>10kb) Multiome | 107 | |
| chr1:168,225,447–168,226,729 | 65.2 kb | Distal (>10kb) Multiome | 1005 |
Genomic view of the TBX19 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.