Entity Details

Primary name BBS2
Entity type gene
Source Source Link

Details

PrimaryID583
RefseqGeneNG_009312
SymbolBBS2
NameBardet-Biedl syndrome 2
Chromosome16
Location16q13
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-05-05
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsBBS2_HUMAN

GO terms

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GOName
GO:0005829 cytosol
GO:0005902 microvillus
GO:0007288 sperm axoneme assembly
GO:0007601 visual perception
GO:0008104 protein localization
GO:0010629 negative regulation of gene expression
GO:0014824 artery smooth muscle contraction
GO:0016020 membrane
GO:0021756 striatum development
GO:0021766 hippocampus development
GO:0021987 cerebral cortex development
GO:0030534 adult behavior
GO:0031514 motile cilium
GO:0032402 melanosome transport
GO:0032420 stereocilium
GO:0033365 protein localization to organelle
GO:0034464 BBSome
GO:0036064 ciliary basal body
GO:0038108 negative regulation of appetite by leptin-mediated signaling pathway
GO:0040015 negative regulation of multicellular organism growth
GO:0040018 positive regulation of multicellular organism growth
GO:0042311 vasodilation
GO:0043001 Golgi to plasma membrane protein transport
GO:0043005 neuron projection
GO:0045444 fat cell differentiation
GO:0045494 photoreceptor cell maintenance
GO:0048854 brain morphogenesis
GO:0051216 cartilage development
GO:0060170 ciliary membrane
GO:0060271 cilium assembly
GO:0060296 regulation of cilium beat frequency involved in ciliary motility
GO:1905515 non-motile cilium assembly

Diseases

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Interactions

4 interactions

InteractorPartnerSourcesPublicationsLink
BBS2Sstr3IntAct20603001 details
BBS2Bbs4IntAct22139371 details
BBS2Bbs7IntAct22139371 details
BBS2Bbs5IntAct22139371 details