Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
Overall Architecture of the Intraflagellar Transport (IFT)-B Complex Containing Cluap1/IFT38 as an Essential Component of the IFT-B Peripheral Subcomplex.
RABL2 interacts with the intraflagellar transport-B complex and CEP19 and participates in ciliary assembly.
The CEP19-RABL2 GTPase Complex Binds IFT-B to Initiate Intraflagellar Transport at the Ciliary Base.
Gene Ontology annotation based on curation of immunofluorescence data
Intrinsic heterogeneity of primary cilia revealed through spatial proteomics.
Annotation inferences using phylogenetic trees
Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans.
Combined Automated Annotation using Multiple IEA Methods
Assembly of the anterograde IFT train
The retrograde IFT train dissociates
Characterization of the intraflagellar transport complex B core: direct interaction of the IFT81 and IFT74/72 subunits.
Intraflagellar transport-A complex mediates ciliary entry and retrograde trafficking of ciliary G protein-coupled receptors.
Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
Differential gene expression during capillary morphogenesis in 3D collagen matrices: regulated expression of genes involved in basement membrane matrix assembly, cell cycle progression, cellular differentiation and G-protein signaling.
Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella.
A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet-Biedl syndrome.
Biochemically validated structural model of the 15-subunit intraflagellar transport complex IFT-B.
Molecular basis of tubulin transport within the cilium by IFT74 and IFT81.
Gene Ontology annotation through association of InterPro records with GO terms
Assembly of the retrograde IFT train
The anterograde IFT train dissociates
Deep research report on IFT74 (Falcon)
Disrupted intraflagellar transport due to IFT74 variants causes Joubert syndrome.