This gene encodes a member of the myosin superfamily. The protein represents an unconventional myosin; it should not be confused with the conventional non-muscle myosin-9 (MYH9). Unconventional myosins contain the basic domains of conventional myosins and are further distinguished from class members by their tail domains. They function as actin-based molecular motors. Mutations in this gene have been associated with Bardet-Biedl Syndrome. [provided by RefSeq, Dec 2011]
Transcription factors with Perturb-seq knockdown data for MYO9A. 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 = MYO9A 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 MYO9A, 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 |
|---|---|---|---|---|
| chr15:72,116,889–72,118,908 | 73 bp | At TSS Multiome | 885 | |
| chr15:72,184,180–72,184,756 | 66.4 kb | Distal (>10kb) Multiome | 376 | |
| chr15:72,196,452–72,198,720 | 79.8 kb | Distal (>10kb) Multiome | 458 | |
| chr15:72,226,391–72,227,225 | 108.8 kb | Distal (>10kb) Multiome | 515 | |
| chr15:72,229,966–72,232,028 | 113.3 kb | Distal (>10kb) Multiome | 1128 | |
| chr15:72,242,418–72,243,365 | 124.9 kb | Distal (>10kb) Multiome | 236 | |
| chr15:72,271,919–72,273,237 | 154.7 kb | Distal (>10kb) Multiome | 687 | |
| chr15:72,319,497–72,320,675 | 202.0 kb | Distal (>10kb) Multiome | 632 | |
| chr15:72,375,551–72,376,566 | 257.9 kb | Distal (>10kb) Multiome | 1074 |
Genomic view of the MYO9A 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.