FANCA
FA complementation group A | FA-H, FAA, FAH, FACA, FANCH

The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group A. Alternative splicing results in multiple transcript variants encoding different isoforms. Mutations in this gene are the most common cause of Fanconi anemia. [provided by RefSeq, Jul 2008]

Member of: DE-6 DE-6.1
Biological processes 18 terms
Expression (TPM)
FANCA — as a Regulated Gene

TFs regulating FANCA 0 TFs

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

Open chromatin peaks (ATAC-seq) in the genomic neighbourhood of FANCA, 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
chr16:89,560,298–89,561,204 256.0 kb Distal (>10kb) Multiome 1030
chr16:89,564,633–89,566,356 250.7 kb Distal (>10kb) Multiome 894
chr16:89,574,359–89,574,949 241.9 kb Distal (>10kb) Multiome 373
chr16:89,657,432–89,658,521 158.8 kb Distal (>10kb) Multiome 859
chr16:89,686,359–89,687,641 129.8 kb Distal (>10kb) Multiome 1006
chr16:89,699,933–89,702,566 114.6 kb Distal (>10kb) Multiome 1079
chr16:89,711,278–89,712,334 104.8 kb Distal (>10kb) Multiome 443
chr16:89,720,440–89,722,486 95.2 kb Distal (>10kb) Multiome 1048
chr16:89,811,423–89,811,615 5.0 kb Proximal (<10kb) 101
chr16:89,816,022–89,817,100 115 bp At TSS Multiome 995
chr16:89,827,667–89,829,190 11.9 kb Distal (>10kb) Multiome 784
chr16:89,872,618–89,874,723 57.6 kb Distal (>10kb) Multiome 1046
chr16:89,917,809–89,919,023 102.0 kb Distal (>10kb) Multiome 986
chr16:89,921,530–89,925,204 106.6 kb Distal (>10kb) Multiome 1006
chr16:89,925,437–89,926,738 109.7 kb Distal (>10kb) Multiome 654
chr16:89,972,039–89,973,313 156.1 kb Distal (>10kb) Multiome 965
chr16:90,018,651–90,020,274 203.0 kb Distal (>10kb) Multiome 634
chr16:90,046,432–90,047,827 230.3 kb Distal (>10kb) Multiome 700
chr16:90,077,247–90,078,026 260.9 kb Distal (>10kb) Multiome 412
chr16:90,081,997–90,082,775 265.6 kb Distal (>10kb) Multiome 755

Genome Browser

Genomic view of the FANCA 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.

chr16:89,550,298 – 90,092,775
Proximal 1 kb Distal 10 kb Multiome HiCAR ATAC-seq RNA-seq