Gene Ontology annotation through association of InterPro records with GO terms

Annotation inferences using phylogenetic trees

Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt

Gene Ontology annotation based on curation of immunofluorescence data

Combined Automated Annotation using Multiple IEA Methods

Centrosome/spindle pole-associated protein regulates cytokinesis via promoting the recruitment of MyoGEF to the central spindle.

Novel asymmetrically localizing components of human centrosomes identified by complementary proteomics methods.

A proteome-scale map of the human interactome network.

A Dynamic Protein Interaction Landscape of the Human Centrosome-Cilium Interface.

Dysfunction of the ciliary ARMC9/TOGARAM1 protein module causes Joubert syndrome.

CCDC66 regulates primary cilium length and signaling via interactions with transition zone and axonemal proteins.

Identification of a novel centrosome/microtubule-associated coiled-coil protein involved in cell-cycle progression and spindle organization.

CSPP and CSPP-L associate with centrosomes and microtubules and differently affect microtubule organization.

Mutations in CSPP1, encoding a core centrosomal protein, cause a range of ciliopathy phenotypes in humans.

Mutations in CSPP1 lead to classical Joubert syndrome.

Mutations in CSPP1 cause primary cilia abnormalities and Joubert syndrome with or without Jeune asphyxiating thoracic dystrophy.

CSPP1 stabilizes growing microtubule ends and damaged lattices from the luminal side.

CSPP1 stabilizes microtubules by capping both plus and minus ends.

CSPP1 selected original-source excerpt and public retrieval locators

A network of interacting ciliary tip proteins with opposing activities imparts slow and processive microtubule growth.