FKBP1A
FKBP prolyl isomerase 1A | FKBP-12, FKBP12, FKBP12C, PKC12, PPIASE, FKBP1

The protein encoded by this gene is a member of the immunophilin protein family, which play a role in immunoregulation and basic cellular processes involving protein folding and trafficking. The protein is a cis-trans prolyl isomerase that binds the immunosuppressants FK506 and rapamycin. It interacts with several intracellular signal transduction proteins including type I TGF-beta receptor. It also interacts with multiple intracellular calcium release channels, and coordinates multi-protein complex formation of the tetrameric skeletal muscle ryanodine receptor. In mouse, deletion of this homologous gene causes congenital heart disorder known as noncompaction of left ventricular myocardium. Multiple alternatively spliced variants, encoding the same protein, have been identified. The human genome contains five pseudogenes related to this gene, at least one of which is transcribed. [provided by RefSeq, Sep 2008]

Member of: DE-1 DE-1.41
Biological processes 50 terms
'de novo' protein folding (GO:0006458)FK506 binding (GO:0005528)FK506 binding (GO:0005528)I-SMAD binding (GO:0070411)T cell activation (GO:0042110)Z disc (GO:0030018)activin receptor binding (GO:0070697)amyloid fibril formation (GO:1990000)calcium channel regulator activity (GO:0005246)cytoplasm (GO:0005737)cytoplasmic side of membrane (GO:0098562)cytosol (GO:0005829)cytosol (GO:0005829)cytosol (GO:0005829)heart morphogenesis (GO:0003007)heart trabecula formation (GO:0060347)macrolide binding (GO:0005527)membrane (GO:0016020)negative regulation of activin receptor signaling pathway (GO:0032926)negative regulation of transforming growth factor beta receptor signaling pathway (GO:0030512)peptidyl-prolyl cis-trans isomerase activity (GO:0003755)peptidyl-prolyl cis-trans isomerase activity (GO:0003755)peptidyl-prolyl cis-trans isomerase activity (GO:0003755)peptidyl-prolyl cis-trans isomerase activity (GO:0003755)positive regulation of canonical NF-kappaB signal transduction (GO:0043123)protein binding (GO:0005515)protein folding (GO:0006457)protein folding (GO:0006457)protein maturation (GO:0051604)protein refolding (GO:0042026)regulation of amyloid precursor protein catabolic process (GO:1902991)regulation of cardiac muscle contraction by regulation of the release of sequestered calcium ion (GO:0010881)regulation of cardiac muscle contraction by regulation of the release of sequestered calcium ion (GO:0010881)regulation of immune response (GO:0050776)regulation of protein localization (GO:0032880)regulation of skeletal muscle contraction by regulation of release of sequestered calcium ion (GO:0014809)ryanodine receptor complex (GO:1990425)sarcoplasmic reticulum (GO:0016529)sarcoplasmic reticulum membrane (GO:0033017)sarcoplasmic reticulum membrane (GO:0033017)signaling receptor inhibitor activity (GO:0030547)supramolecular fiber organization (GO:0097435)terminal cisterna (GO:0014802)transforming growth factor beta receptor binding (GO:0005160)transforming growth factor beta receptor binding (GO:0005160)transmembrane transporter binding (GO:0044325)transmembrane transporter binding (GO:0044325)type I transforming growth factor beta receptor binding (GO:0034713)type I transforming growth factor beta receptor binding (GO:0034713)ventricular cardiac muscle tissue morphogenesis (GO:0055010)
Expression (TPM)
FKBP1A — as a Regulated Gene

TFs regulating FKBP1A 0 TFs

Transcription factors with Perturb-seq knockdown data for FKBP1A. 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 = FKBP1A 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 FKBP1A

Open chromatin peaks (ATAC-seq) in the genomic neighbourhood of FKBP1A, 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
chr20:1,118,327–1,119,071 274.6 kb Distal (>10kb) Multiome 1066
chr20:1,184,818–1,186,197 207.4 kb Distal (>10kb) Multiome 557
chr20:1,225,365–1,226,806 167.3 kb Distal (>10kb) Multiome 616
chr20:1,266,029–1,266,958 126.7 kb Distal (>10kb) Multiome 499
chr20:1,300,911–1,301,500 91.9 kb Distal (>10kb) Multiome 171
chr20:1,313,163–1,313,790 79.6 kb Distal (>10kb) Multiome 428
chr20:1,325,008–1,326,107 67.7 kb Distal (>10kb) Multiome 901
chr20:1,391,813–1,391,980 1.2 kb Proximal (<10kb) 147
chr20:1,392,628–1,393,457 52 bp At TSS Multiome 799
chr20:1,427,438–1,428,145 34.6 kb Distal (>10kb) Multiome 285
chr20:1,466,316–1,467,471 73.7 kb Distal (>10kb) Multiome 1054

Genome Browser

Genomic view of the FKBP1A 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.

chr20:1,108,327 – 1,477,471
Proximal 1 kb Distal 10 kb Multiome HiCAR ATAC-seq RNA-seq