Entity Details

Primary name BBS7
Entity type gene
Source Source Link

Details

PrimaryID55212
RefseqGeneNG_009111
SymbolBBS7
NameBardet-Biedl syndrome 7
Chromosome4
Location4q27
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2000-07-03
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsBBS7_HUMAN

GO terms

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GOName
GO:0001654 eye development
GO:0001750 photoreceptor outer segment
GO:0001947 heart looping
GO:0005634 nucleus
GO:0005813 centrosome
GO:0005829 cytosol
GO:0005930 axoneme
GO:0006357 regulation of transcription by RNA polymerase II
GO:0007224 smoothened signaling pathway
GO:0007368 determination of left/right symmetry
GO:0007420 brain development
GO:0007601 visual perception
GO:0008104 protein localization
GO:0015031 protein transport
GO:0016020 membrane
GO:0032402 melanosome transport
GO:0032436 positive regulation of proteasomal ubiquitin-dependent protein catabolic process
GO:0034464 BBSome
GO:0036064 ciliary basal body
GO:0043005 neuron projection
GO:0045444 fat cell differentiation
GO:0046907 intracellular transport
GO:0048546 digestive tract morphogenesis
GO:0051877 pigment granule aggregation in cell center
GO:0060170 ciliary membrane
GO:0060173 limb development
GO:0060271 cilium assembly
GO:1903929 primary palate development
GO:1905515 non-motile cilium assembly

Diseases

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Interactions

2 interactions

InteractorPartnerSourcesPublicationsLink
BBS7Sstr3IntAct20603001 details
BBS7SmoIntAct22072986 details