about
P688
BBS6, BBS10, and BBS12 form a complex with CCT/TRiC family chaperonins and mediate BBSome assemblyA novel protein LZTFL1 regulates ciliary trafficking of the BBSome and SmoothenedBardet-Biedl syndrome 3 (Bbs3) knockout mouse model reveals common BBS-associated phenotypes and Bbs3 unique phenotypesBBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypesIntrinsic protein-protein interaction-mediated and chaperonin-assisted sequential assembly of stable bardet-biedl syndrome protein complex, the BBSomeRequirement of Bardet-Biedl syndrome proteins for leptin receptor signalingLoss of Bardet-Biedl syndrome proteins alters the morphology and function of motile cilia in airway epitheliaThe centriolar satellite protein AZI1 interacts with BBS4 and regulates ciliary trafficking of the BBSomeThe BBSome controls IFT assembly and turnaround in cilia.Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin.Bardet-Biedl syndrome proteins are required for the localization of G protein-coupled receptors to primary ciliaLeptin resistance contributes to obesity and hypertension in mouse models of Bardet-Biedl syndromeCiliary proteins Bbs8 and Ift20 promote planar cell polarity in the cochleaA knockin mouse model of the Bardet-Biedl syndrome 1 M390R mutation has cilia defects, ventriculomegaly, retinopathy, and obesityCartilage abnormalities associated with defects of chondrocytic primary cilia in Bardet-Biedl syndrome mutant mice.Temporal expression pattern of Bardet-Biedl syndrome genes in adipogenesisDAZ-interacting Protein 1 (Dzip1) Phosphorylation by Polo-like Kinase 1 (Plk1) Regulates the Centriolar Satellite Localization of the BBSome Protein during the Cell Cycle.
P921
Q24295491-FAF1862A-109C-402C-A7F6-85DDBA66A3D9Q24296671-2D4C6218-9BB8-4712-9BE8-468B74FE1B48Q24298940-3DC0B993-856D-4972-96F9-05092DE01B56Q24301377-C0AAABD2-9C7E-49B9-BF50-F910DAAA4249Q24313282-4BE7DE1C-E0EA-41F8-B466-3AA4AC8B3D8CQ24317488-B1F5126F-4500-4272-A23B-BA1F468902C0Q24317556-08627E8E-2054-4FE3-95B2-8ABDE62138CCQ24337792-566DD6F6-E4C0-430F-BD96-B7E5D9012458Q28000109-28420291-8CF4-46C7-88F6-FB6DF9E157FEQ28292806-34C6FFF5-7A3B-4B4B-A11C-0129CA66D235Q28506905-8269F71A-68B4-457B-8CB2-3D9DE69B40BFQ28511291-511D9D52-B71F-4D69-9EDF-8EED73B0ABAAQ28512858-5B5A1135-E963-4554-8075-FD7B72626D4DQ28513461-65D7BFF3-5E5A-4402-99C6-0A0B07B5497EQ28594558-2CEBC7FE-828C-470C-8C94-B7F34FE88DDBQ28595018-B4BDA547-A782-4772-ACF5-235BB8F1B6CCQ42804683-35CCAE76-52A5-494E-86CD-C6CD2A3DEC0A
P921
description
mammalian protein found in Mus musculus
@en
protein
@id
proteinë
@sq
proteïne in Bardet-Biedl syndrome 2 (human)
@nl
protèin
@ace
بروتين في فأر المنازل
@ar
name
Bardet-Biedl syndrome 2 (human)
@en
Bardet-Biedl syndrome 2
@nl
type
label
Bardet-Biedl syndrome 2 (human)
@en
Bardet-Biedl syndrome 2
@nl
altLabel
Bardet-Biedl syndrome 2 homolog
@en
Bardet-Biedl syndrome 2 protein homolog
@en
Bbs2
@en
prefLabel
Bardet-Biedl syndrome 2 (human)
@en
Bardet-Biedl syndrome 2
@nl
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XP_006531367
XP_030099595
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ENSMUSP00000034206