ATP11C
ATPase phospholipid transporting 11C (ATP11C blood group) | ATPIG, ATPIQ

Enables phosphatidylethanolamine flippase activity and phosphatidylserine flippase activity. Involved in phospholipid translocation. Located in endoplasmic reticulum and plasma membrane. Part of phospholipid-translocating ATPase complex. Implicated in X-linked congenital hemolytic anemia. [provided by Alliance of Genome Resources, Jul 2025]

Member of: DE-3 DE-3.9 Developmental clusters: GC4
Biological processes 34 terms
Expression (TPM)
ATP11C — as a Regulated Gene

TFs regulating ATP11C 0 TFs

Transcription factors with Perturb-seq knockdown data for ATP11C. 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 = ATP11C 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 ATP11C

Open chromatin peaks (ATAC-seq) in the genomic neighbourhood of ATP11C, 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
chrX:139,931,285–139,931,654 1.4 kb Proximal (<10kb) 183
chrX:139,931,948–139,933,886 70 bp At TSS Multiome 618
chrX:139,936,404–139,936,562 3.4 kb Proximal (<10kb) 16
chrX:139,936,692–139,936,833 3.6 kb Proximal (<10kb) 10

Genome Browser

Genomic view of the ATP11C 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.

chrX:139,921,285 – 139,946,833
Proximal 1 kb Distal 10 kb Multiome HiCAR ATAC-seq RNA-seq