About: cilium assembly

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

A process that is carried out at the cellular level and in which the structure of a cilium is organized.

Attributes	Values
rdf:type	Item
description	A process that is carried out at the cellular level and in which the structure of a cilium is organized. (en)
exact match	wds:Q14916348-08E3CCCF-BCC8-464C-B973-41A693D6145D
exact match	http://purl.obolibrary.org/obo/GO_0060271
rdfs:label	cilium assembly (en)
skos:prefLabel	cilium assembly (en)
name	cilium assembly (en)
Gene Ontology ID	wds:Q14916348-DB8CCF29-6C59-4A29-B0A3-2968B4B91303
Gene Ontology ID	GO:0060271
instance of	wds:Q14916348-2CA5CB3A-20DF-43BA-9881-D31B8D7B6EAF
instance of	biological process
subclass of	wds:Q14916348-1FBB2D51-53CA-4CD7-9BB8-4E356D1487E7 wds:Q14916348-7883D2A3-46CE-4FCB-B7D6-BED4EC3D55F4 wds:Q14916348-D8342F49-4DEF-4CAD-B938-0D73C0D59C02
subclass of	organelle assembly cilium organization plasma membrane bounded cell projection assembly
has part(s)	wds:Q14916348-12A91BBA-0662-4E84-AC57-6FFCDBCB1C05 wds:Q14916348-2427C467-52F6-4715-A1E6-42ECD29675E4 wds:Q14916348-320ED2BD-67FF-4652-8D0E-0CC35EF17C68 wds:Q14916348-8F2913B3-F67E-4329-97F2-79D8EDDC2163 wds:Q14916348-BF8BF131-27C3-4367-A668-623DFB60CE46
has part(s)	axoneme assembly intraciliary transport involved in cilium assembly vesicle targeting, trans-Golgi to periciliary membrane compartment protein localization to cilium ciliary transition zone assembly
skos:altLabel	GO:0060271 (en) ciliogenesis (en) cilium formation (en) microtubule-based flagellum assembly (en)
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q14916348
is instance of of	VxPx cargo-targeting to cilium BBSome-mediated cargo-targeting to cilium Trafficking of myristoylated proteins to the cilium ARL13B-mediated ciliary trafficking of INPP5E Cilium Assembly Cargo trafficking to the periciliary membrane
is part of of	ciliary basal body-plasma membrane docking axoneme assembly intraciliary transport involved in cilium assembly vesicle targeting, trans-Golgi to periciliary membrane compartment ciliary transition zone assembly ciliary centrin arm assembly
is instance of of	wds:Q45317876-6E3B76D7-2E41-4A2C-AF2D-9FC6CE721270 wds:Q45317878-8AFE6500-15CA-47FC-B6B4-5D51401AF8F9 wds:Q45317879-A6F8440A-CC7B-4E11-9554-BA20F45C6DEC wds:Q45317877-8FCB6201-E159-4B81-AADE-B9E66D74F8C7 wds:Q45317874-EBFE7B0E-2FCE-4326-BB9D-80229DFD16E6 wds:Q45317881-3DCCFB07-8F6F-4843-94D9-5EC93C17B1CD
is part of of	wds:Q26452783-66A1AE11-82A1-4FDA-84A7-FB7548925F0F wds:Q26452785-C68B5D8D-2AB7-47CF-9B5A-15ACB5388B53 wds:Q26470136-ED0F4898-B93C-4152-A8B8-3695B2C9CD97 wds:Q21112023-B02D6F9E-668A-453A-926F-966832B0B77D wds:Q112997985-E7711170-F5DD-4F1E-8BCD-10DE723D1A73 wds:Q21100675-C7562C6C-0FA8-4512-8212-ADFFF56562C4
is subclass of of	non-motile cilium assembly motile cilium assembly cytosolic ciliogenesis
is subclass of of	wds:Q28598513-390F33B2-795D-425B-863F-78607FC7CA91 wds:Q27118859-F7352874-70A7-4B45-A2FE-606C85E99A45 wds:Q21105422-53A146D9-7D03-45F0-A4DB-3CE4255F58F6
is main subject of	A SNX10/V-ATPase pathway regulates ciliogenesis in vitro and in vivo Subunit composition of the human cytoplasmic dynein-2 complex Tctex1d2 associates with short-rib polydactyly syndrome proteins and is required for ciliogenesis A common variant in combination with a nonsense mutation in a member of the thioredoxin family causes primary ciliary dyskinesia Murine cytomegalovirus influences Foxj1 expression, ciliogenesis, and mucus plugging in mice with allergic airway disease Distinct isoforms of the RFX transcription factor DAF-19 regulate ciliogenesis and maintenance of synaptic activity Small molecule inhibitors of Smoothened ciliary localization and ciliogenesis The NIMA-family kinase, Nek1 affects the stability of centrosomes and ciliogenesis Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesis A BBSome subunit links ciliogenesis, microtubule stability, and acetylation Two miRNA clusters, miR-34b/c and miR-449, are essential for normal brain development, motile ciliogenesis, and spermatogenesis The role of RPGR in cilia formation and actin stability Pathogenic NPHP5 mutations impair protein interaction with Cep290, a prerequisite for ciliogenesis miR-34/449 miRNAs are required for motile ciliogenesis by repressing cp110. Ciliogenesis and centriole formation in the mouse embryonic nervous system. An ultrastructural analysis The Nek8 protein kinase, mutated in the human cystic kidney disease nephronophthisis, is both activated and degraded during ciliogenesis Ciliogenesis and cerebrospinal fluid flow in the developing Xenopus brain are regulated by foxj1 CEP41 is mutated in Joubert syndrome and is required for tubulin glutamylation at the cilium Evolutionarily assembled cis-regulatory module at a human ciliopathy locus Combining Cep290 and Mkks ciliopathy alleles in mice rescues sensory defects and restores ciliogenesis A transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition ATMIN is a transcriptional regulator of both lung morphogenesis and ciliogenesis Identification of FOXJ1 effectors during ciliogenesis in the foetal respiratory epithelium and embryonic left-right organiser of the mouse Differential regulation of centrin genes during ciliogenesis in human tracheal epithelial cells The sequence and analysis of duplication-rich human chromosome 16 Nesprin-2 interacts with meckelin and mediates ciliogenesis via remodelling of the actin cytoskeleton Basal body stability and ciliogenesis requires the conserved component Poc1 Centriolar kinesin Kif24 interacts with CP110 to remodel microtubules and regulate ciliogenesis Ubiquitin-proteasome system controls ciliogenesis at the initial step of axoneme extension A novel Crumbs3 isoform regulates cell division and ciliogenesis via importin beta interactions Nde1-mediated inhibition of ciliogenesis affects cell cycle re-entry Induction of Ran GTP drives ciliogenesis Insufficiency of BUBR1, a mitotic spindle checkpoint regulator, causes impaired ciliogenesis in vertebrates. A new cellular stress response that triggers centriolar satellite reorganization and ciliogenesis The human dynein intermediate chain 2 gene (DNAI2): cloning, mapping, expression pattern, and evaluation as a candidate for primary ciliary dyskinesia FAM161A, associated with retinitis pigmentosa, is a component of the cilia-basal body complex and interacts with proteins involved in ciliopathies Bardet-Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia function miR-129-3p controls cilia assembly by regulating CP110 and actin dynamics

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