BBS4

BBS4
Identifiers
Aliases	BBS4, Bardet-Biedl syndrome 4
External IDs	OMIM: 600374; MGI: 2143311; HomoloGene: 13197; GeneCards: BBS4; OMA:BBS4 - orthologs
Gene location (Human) Chr. Chromosome 15 (human) Band 15q24.1 Start 72,686,179 bp End 72,738,475 bp
Gene location (Mouse) Chr. Chromosome 9 (mouse) Band 9 B|9 32.01 cM Start 59,229,273 bp End 59,260,791 bp
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in right uterine tube oocyte secondary oocyte anterior pituitary right lobe of thyroid gland ventricular zone left ovary left lobe of thyroid gland right testis left testis Top expressed in primary oocyte spermatocyte zygote secondary oocyte spermatid olfactory epithelium neural layer of retina dorsomedial hypothalamic nucleus facial motor nucleus epithelium of lens More reference expression data BioGPS More reference expression data
Gene ontology Molecular function microtubule motor activity dynactin binding alpha-tubulin binding protein binding beta-tubulin binding Cellular component cytoplasm ciliary basal body centrosome cell projection BBSome pericentriolar material membrane photoreceptor inner segment plasma membrane photoreceptor outer segment cilium centriolar satellite ciliary transition zone photoreceptor connecting cilium microtubule organizing center ciliary membrane centriole motile cilium cytoskeleton nucleus cytosol non-motile cilium Biological process protein localization to organelle fat pad development cilium assembly regulation of cilium beat frequency involved in ciliary motility protein localization regulation of cytokinesis negative regulation of actin filament polymerization negative regulation of appetite by leptin-mediated signaling pathway response to stimulus leptin-mediated signaling pathway dendrite development mitotic cytokinesis sensory processing intracellular transport neuron migration photoreceptor cell outer segment organization negative regulation of gene expression ventricular system development regulation of stress fiber assembly protein localization to photoreceptor outer segment heart looping sensory perception of smell regulation of lipid metabolic process face development neural tube closure retina homeostasis adult behavior negative regulation of GTPase activity cell projection organization protein localization to cilium melanosome transport retinal rod cell development spermatid development positive regulation of multicellular organism growth cerebral cortex development protein transport social behavior protein localization to centrosome positive regulation of cilium assembly photoreceptor cell maintenance regulation of non-motile cilium assembly response to leptin negative regulation of systemic arterial blood pressure hippocampus development fat cell differentiation microtubule cytoskeleton organization maintenance of protein location in nucleus striatum development microtubule anchoring at centrosome visual perception brain morphogenesis non-motile cilium assembly centrosome cycle Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 585 102774 Ensembl ENSG00000140463 ENSMUSG00000025235 UniProt Q96RK4 Q8C1Z7 RefSeq (mRNA) NM_001252678 NM_033028 NM_001320665 NM_175325 NM_001359558 RefSeq (protein) NP_001239607 NP_001307594 NP_149017 NP_780534 NP_001346487 Location (UCSC) Chr 15: 72.69 – 72.74 Mb Chr 9: 59.23 – 59.26 Mb PubMed search
Wikidata
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Bardet–Biedl syndrome 4 is a protein that in humans is encoded by the BBS4 gene.

This gene encodes a protein which contains tetratricopeptide repeats (TPR), similar to O-linked N-acetylglucosamine transferase. Mutations in this gene have been observed in patients with Bardet–Biedl syndrome type 4. The encoded protein may play a role in pigmentary retinopathy, obesity, polydactyly, renal malformation and mental retardation.

Interactions

BBS4 has been shown to interact with DCTN1.

Further reading

• Haftek J, Krawczykowa Z, Stankiewicz A, Araszkiewicz H, Goś R, Kasprzak H (June 1975). "[Ocular manifestations in orbital fractures]". Klinika Oczna. 45 (6): 655–9. PMID 1138127.
• Bruford EA, Riise R, Teague PW, Porter K, Thomson KL, Moore AT, Jay M, Warburg M, Schinzel A, Tommerup N, Tornqvist K, Rosenberg T, Patton M, Mansfield DC, Wright AF (Apr 1997). "Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21". Genomics. 41 (1): 93–9. doi:10.1006/geno.1997.4613. PMID 9126487.
• Katsanis N, Eichers ER, Ansley SJ, Lewis RA, Kayserili H, Hoskins BE, Scambler PJ, Beales PL, Lupski JR (Jul 2002). "BBS4 is a minor contributor to Bardet-Biedl syndrome and may also participate in triallelic inheritance". American Journal of Human Genetics. 71 (1): 22–9. doi:10.1086/341031. PMC 384990. PMID 12016587.
• Riise R, Tornqvist K, Wright AF, Mykytyn K, Sheffield VC (Oct 2002). "The phenotype in Norwegian patients with Bardet-Biedl syndrome with mutations in the BBS4 gene". Archives of Ophthalmology. 120 (10): 1364–7. doi:10.1001/archopht.120.10.1364. PMID 12365916.
• Hoskins BE, Thorn A, Scambler PJ, Beales PL (August 2003). "Evaluation of multiplex capillary heteroduplex analysis: a rapid and sensitive mutation screening technique". Human Mutation. 22 (2): 151–7. doi:10.1002/humu.10241. PMID 12872256. S2CID 30935841.
• Kim JC, Badano JL, Sibold S, Esmail MA, Hill J, Hoskins BE, Leitch CC, Venner K, Ansley SJ, Ross AJ, Leroux MR, Katsanis N, Beales PL (May 2004). "The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression". Nature Genetics. 36 (5): 462–70. doi:10.1038/ng1352. PMID 15107855.
• Ye X, Dai J, Fang W, Jin W, Guo Y, Song J, Ji C, Gu S, Xie Y, Mao Y (June 2004). "Cloning and characterization of a splice variant of human Bardet-Biedl syndrome 4 gene (BBS4)". DNA Sequence. 15 (3): 213–8. doi:10.1080/10425170410001679165. PMID 15497446. S2CID 12549938.
• Rual JF, Venkatesan K, Hao T, Hirozane-Kishikawa T, Dricot A, Li N, Berriz GF, Gibbons FD, Dreze M, Ayivi-Guedehoussou N, Klitgord N, Simon C, Boxem M, Milstein S, Rosenberg J, Goldberg DS, Zhang LV, Wong SL, Franklin G, Li S, Albala JS, Lim J, Fraughton C, Llamosas E, Cevik S, Bex C, Lamesch P, Sikorski RS, Vandenhaute J, Zoghbi HY, Smolyar A, Bosak S, Sequerra R, Doucette-Stamm L, Cusick ME, Hill DE, Roth FP, Vidal M (Oct 2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–8. Bibcode:2005Natur.437.1173R. doi:10.1038/nature04209. PMID 16189514. S2CID 4427026.

External links

• GeneReviews/NIH/NCBI/UW entry on Bardet-Biedl Syndrome
• Human BBS4 genome location and BBS4 gene details page in the UCSC Genome Browser.