BBS4
Bardet-Biedl syndrome 4

This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation and cognitive disability. The proteins encoded by BBS gene family members are structurally diverse. The similar phenotypes exhibited by mutations in BBS gene family members are likely due to the protein's shared roles in cilia formation and function. Many BBS proteins localize to the basal bodies, ciliary axonemes, and pericentriolar regions of cells. BBS proteins may also be involved in intracellular trafficking via microtubule-related transport. The protein encoded by this gene has sequence similarity to O-linked N-acetylglucosamine (O-GlcNAc) transferases in plants and archaebacteria and in human forms a multi-protein "BBSome" complex with seven other BBS proteins. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]

Member of: DE-5
Biological processes 73 terms
BBSome (GO:0034464)BBSome (GO:0034464)RNA polymerase II-specific DNA-binding transcription factor binding (GO:0061629)adult behavior (GO:0030534)alpha-tubulin binding (GO:0043014)beta-tubulin binding (GO:0048487)brain morphogenesis (GO:0048854)centriolar satellite (GO:0034451)centriolar satellite (GO:0034451)centriole (GO:0005814)centrosome (GO:0005813)centrosome (GO:0005813)centrosome cycle (GO:0007098)cerebral cortex development (GO:0021987)ciliary basal body (GO:0036064)ciliary basal body (GO:0036064)ciliary membrane (GO:0060170)ciliary membrane (GO:0060170)ciliary transition zone (GO:0035869)ciliary transition zone (GO:0035869)cilium (GO:0005929)cilium (GO:0005929)cilium assembly (GO:0060271)cilium assembly (GO:0060271)cilium assembly (GO:0060271)cilium assembly (GO:0060271)cytoplasm (GO:0005737)cytosol (GO:0005829)dendrite development (GO:0016358)dynactin binding (GO:0034452)fat cell differentiation (GO:0045444)fat cell differentiation (GO:0045444)heart looping (GO:0001947)hippocampus development (GO:0021766)maintenance of protein location in nucleus (GO:0051457)melanosome transport (GO:0032402)membrane (GO:0016020)microtubule anchoring at centrosome (GO:0034454)microtubule cytoskeleton organization (GO:0000226)microtubule cytoskeleton organization (GO:0000226)mitotic cytokinesis (GO:0000281)motile cilium (GO:0031514)motile cilium (GO:0031514)negative regulation of appetite by leptin-mediated signaling pathway (GO:0038108)negative regulation of appetite by leptin-mediated signaling pathway (GO:0038108)neural tube closure (GO:0001843)non-motile cilium (GO:0097730)non-motile cilium (GO:0097730)non-motile cilium assembly (GO:1905515)nucleus (GO:0005634)pericentriolar material (GO:0000242)photoreceptor cell maintenance (GO:0045494)photoreceptor connecting cilium (GO:0032391)photoreceptor inner segment (GO:0001917)photoreceptor outer segment (GO:0001750)positive regulation of cilium assembly (GO:0045724)protein binding (GO:0005515)protein localization to centrosome (GO:0071539)protein localization to cilium (GO:0061512)protein localization to cilium (GO:0061512)protein localization to cilium (GO:0061512)protein-macromolecule adaptor activity (GO:0030674)regulation of cilium beat frequency involved in ciliary motility (GO:0060296)regulation of cilium beat frequency involved in ciliary motility (GO:0060296)regulation of cytokinesis (GO:0032465)regulation of lipid metabolic process (GO:0019216)retina homeostasis (GO:0001895)retinal rod cell development (GO:0046548)sensory perception (GO:0007600)sensory perception of smell (GO:0007608)sensory processing (GO:0050893)spermatid development (GO:0007286)striatum development (GO:0021756)
Expression (TPM)
BBS4 — as a Regulated Gene

TFs regulating BBS4 0 TFs

Transcription factors with Perturb-seq knockdown data for BBS4. 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 = BBS4 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 BBS4

Open chromatin peaks (ATAC-seq) in the genomic neighbourhood of BBS4, 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
chr15:72,473,670–72,475,497 212.0 kb Distal (>10kb) Multiome 1105
chr15:72,783,062–72,784,628 97.6 kb Distal (>10kb) Multiome 1026
chr15:72,796,497–72,797,516 110.9 kb Distal (>10kb) Multiome 460

Genome Browser

Genomic view of the BBS4 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.

chr15:72,463,670 – 72,807,516
Proximal 1 kb Distal 10 kb Multiome HiCAR ATAC-seq RNA-seq