SLC2A13
solute carrier family 2 member 13 | HMIT

Enables ATPase binding activity; myo-inositol:proton symporter activity; and protease binding activity. Involved in myo-inositol transport and positive regulation of amyloid-beta formation. Located in cell body; cell projection; and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]

Member of: DE-3
Biological processes 45 terms
Expression (TPM)
SLC2A13 — as a Regulated Gene

TFs regulating SLC2A13 0 TFs

Transcription factors with Perturb-seq knockdown data for SLC2A13. 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 = SLC2A13 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 SLC2A13

Open chromatin peaks (ATAC-seq) in the genomic neighbourhood of SLC2A13, 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
chr12:40,101,354–40,102,063 4.0 kb Proximal (<10kb) 30
chr12:40,103,064–40,103,590 2.5 kb Proximal (<10kb) 37
chr12:40,104,828–40,106,955 27 bp At TSS Multiome 706
chr12:40,107,069–40,107,294 988 bp At TSS 35
chr12:40,107,440–40,108,010 1.4 kb Proximal (<10kb) 364

Genome Browser

Genomic view of the SLC2A13 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.

chr12:40,091,354 – 40,118,010
Proximal 1 kb Distal 10 kb Multiome HiCAR ATAC-seq RNA-seq