about
Doublecortin domain containing 2aOCRL, inositol polyphosphate-5-phosphataseDisrupted in schizophrenia 1Chibby family member 2Male germ cell associated kinaseEH domain containing 1ADP ribosylation factor like GTPase 3ADP ribosylation factor like GTPase 6Centrosomal protein 126Cilia and flagella associated protein 52Cilia and flagella associated protein 44Cilia and flagella associated protein 20Forkhead box J1CBY1 interacting BAR domain containing 1Chibby family member 3Cilia and flagella associated protein 53Coiled-coil domain containing 113Chibby family member 1, beta catenin antagonistTransmembrane protein 250Clusterin associated protein 1Dynein cytoplasmic 2 heavy chain 1Regulatory factor X3FH2 domain containing 1Laminin subunit alpha 5Actin binding LIM protein family member 3ArfGAP with SH3 domain, ankyrin repeat and PH domain 1Coiled-coil domain containing 28BBardet-Biedl syndrome 9Bardet-Biedl syndrome 5McKusick-Kaufman syndromeDynein axonemal assembly factor 1E2F transcription factor 4NIMA related kinase 1ADP ribosylation factor like GTPase 13BSorting nexin 10Cilia and flagella associated protein 410Dynein 2 intermediate chain 2NudC domain containing 3Centrosomal protein 20WD repeat containing planar cell polarity effector
P682
A role for Alström syndrome protein, alms1, in kidney ciliogenesis and cellular quiescenceBasal body stability and ciliogenesis requires the conserved component Poc1Characterization of an axonemal dynein heavy chain expressed early in airway epithelial ciliogenesisThe human dynein intermediate chain 2 gene (DNAI2): cloning, mapping, expression pattern, and evaluation as a candidate for primary ciliary dyskinesiaCiliogenesis is regulated by a huntingtin-HAP1-PCM1 pathway and is altered in Huntington diseaseThe intraflagellar transport protein IFT20 is associated with the Golgi complex and is required for cilia assemblyC14ORF179 encoding IFT43 is mutated in Sensenbrenner syndromePrimary ciliogenesis requires the distal appendage component Cep123.ICK is essential for cell type-specific ciliogenesis and the regulation of ciliary transportCcdc13 is a novel human centriolar satellite protein required for ciliogenesis and genome stabilityFAM161A, associated with retinitis pigmentosa, is a component of the cilia-basal body complex and interacts with proteins involved in ciliopathiesCep164, a novel centriole appendage protein required for primary cilium formationA meckelin-filamin A interaction mediates ciliogenesisTMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zoneHuman and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesisCharacterization of CCDC28B reveals its role in ciliogenesis and provides insight to understand its modifier effect on Bardet-Biedl syndromeA common variant in combination with a nonsense mutation in a member of the thioredoxin family causes primary ciliary dyskinesiaBardet-Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia functionThe Lowe syndrome protein OCRL1 is involved in primary cilia assemblyProteomic analysis of mammalian sperm cells identifies new components of the centrosomeBardet-Biedl syndrome-associated small GTPase ARL6 (BBS3) functions at or near the ciliary gate and modulates Wnt signalingCEP41 is mutated in Joubert syndrome and is required for tubulin glutamylation at the ciliumThe spinocerebellar ataxia-associated gene Tau tubulin kinase 2 controls the initiation of ciliogenesisEvolutionarily assembled cis-regulatory module at a human ciliopathy locusCentriolar kinesin Kif24 interacts with CP110 to remodel microtubules and regulate ciliogenesisUbiquitin-proteasome system controls ciliogenesis at the initial step of axoneme extensionAxonemal localization of the dynein component DNAH5 is not altered in secondary ciliary dyskinesiaFunctional genomic screen for modulators of ciliogenesis and cilium lengthCombining Cep290 and Mkks ciliopathy alleles in mice rescues sensory defects and restores ciliogenesisThe Zn finger protein Iguana impacts Hedgehog signaling by promoting ciliogenesisThe novel centriolar satellite protein SSX2IP targets Cep290 to the ciliary transition zoneThe microtubule affinity regulating kinase MARK4 promotes axoneme extension during early ciliogenesis.HIF1α deubiquitination by USP8 is essential for ciliogenesis in normoxiaOCRL localizes to the primary cilium: a new role for cilia in Lowe syndromeEarly steps in primary cilium assembly require EHD1/EHD3-dependent ciliary vesicle formationBug22 influences cilium morphology and the post-translational modification of ciliary microtubulesMolecular basis of tubulin transport within the cilium by IFT74 and IFT81.A SNX10/V-ATPase pathway regulates ciliogenesis in vitro and in vivoNEK1 mutations cause short-rib polydactyly syndrome type majewskiC2orf62 and TTC17 are involved in actin organization and ciliogenesis in zebrafish and human
P921
description
A process that is carried out ...... ture of a cilium is organized.
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name
cilium morphogenesis
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type
label
cilium morphogenesis
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altLabel
GO:0060271
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ciliogenesis
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cilium assembly
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cilium formation
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microtubule-based flagellum assembly
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prefLabel
cilium morphogenesis
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P279
P527
P2888
P527
P686
GO:0060271