about
P688
Combining Cep290 and Mkks ciliopathy alleles in mice rescues sensory defects and restores ciliogenesisBBS mutations modify phenotypic expression of CEP290-related ciliopathiesThe centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4CP110 suppresses primary cilia formation through its interaction with CEP290, a protein deficient in human ciliary diseaseCep120 and TACCs control interkinetic nuclear migration and the neural progenitor pool.In-frame deletion in a novel centrosomal/ciliary protein CEP290/NPHP6 perturbs its interaction with RPGR and results in early-onset retinal degeneration in the rd16 mouseAcute versus chronic loss of mammalian Azi1/Cep131 results in distinct ciliary phenotypesA transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition.Primary cilia control hedgehog signaling during muscle differentiation and are deregulated in rhabdomyosarcoma3D spheroid defects in NPHP knockdown cells are rescued by the somatostatin receptor agonist octreotideHypomorphic CEP290/NPHP6 mutations result in anosmia caused by the selective loss of G proteins in cilia of olfactory sensory neurons.DAZ-interacting Protein 1 (Dzip1) Phosphorylation by Polo-like Kinase 1 (Plk1) Regulates the Centriolar Satellite Localization of the BBSome Protein during the Cell Cycle.SPATA7 maintains a novel photoreceptor-specific zone in the distal connecting cilium.
P921
Q24309344-FDDE3FDB-3799-40EE-989D-0C577771DB8FQ24317466-4D7F2B2C-71AF-4A1B-AB69-74DFA664F9BEQ24336477-E8820ED5-590B-4608-B014-80C819E548BBQ24568058-92053E67-4AD2-46DE-ADFE-8F82C9B4B680Q24653494-89F5FCB3-DDD2-4D35-AE39-F3C3C5021DE0Q24671808-60744B41-B286-49CA-8F5E-CCEB88384389Q27319882-7D43C6B1-550C-4078-84BC-787E66483091Q28000057-1A517364-83E8-4AD2-9A44-F66DB4DFE689Q28512043-853ACC8B-B60B-4FA6-ADB7-BD74AA13BC35Q28591854-C0EE5E23-6F6F-4E0B-933B-7C16819F135BQ36023714-5470B1E8-6E8D-4AC0-B936-FDB9C94A7C10Q42804683-22BD27FA-B73A-423A-B161-6AB407BAE17BQ64961358-813F799A-B5E3-4725-B7B6-E76D2E83AA3B
P921
description
mammalian protein found in Mus musculus
@en
protein
@id
proteinë
@sq
proteïne in Centrosomal protein 290
@nl
protèin
@ace
بروتين في فأر المنازل
@ar
name
Centrosomal protein 290
@en
type
label
Centrosomal protein 290
@en
altLabel
Bardet-Biedl syndrome 14 protein homolog
@en
Cep290
@en
centrosomal protein of 290 kDa
@en
nephrocystin-6
@en
prefLabel
Centrosomal protein 290
@en
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ENSMUSP00000130899
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