SLC9A9
solute carrier family 9 member A9 | FLJ35613, NHE9

This gene encodes a sodium/proton exchanger that is a member of the solute carrier 9 protein family. The encoded protein localizes the to the late recycling endosomes and may play an important role in maintaining cation homeostasis. Mutations in this gene are associated with autism susceptibility 16 and attention-deficit/hyperactivity disorder. [provided by RefSeq, Mar 2012]

Member of: DE-9 DE-9.1
Biological processes 38 terms
Expression (TPM)
SLC9A9 — as a Regulated Gene

TFs regulating SLC9A9 0 TFs

Transcription factors with Perturb-seq knockdown data for SLC9A9. 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 = SLC9A9 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 SLC9A9

Open chromatin peaks (ATAC-seq) in the genomic neighbourhood of SLC9A9, 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
chr3:143,805,063–143,806,295 42.8 kb Distal (>10kb) Multiome 164
chr3:143,839,907–143,840,281 8.2 kb Proximal (<10kb) 41
chr3:143,846,931–143,847,349 1.1 kb Proximal (<10kb) 10
chr3:143,847,763–143,848,060 424 bp At TSS 152
chr3:143,848,219–143,848,571 at TSS At TSS 161
chr3:143,970,615–143,973,789 123.3 kb Distal (>10kb) Multiome 1038

Genome Browser

Genomic view of the SLC9A9 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.

chr3:143,795,063 – 143,983,789
Proximal 1 kb Distal 10 kb Multiome HiCAR ATAC-seq RNA-seq