The Meckel-Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation.

Ciliary and centrosomal defects associated with mutation and depletion of the Meckel syndrome genes MKS1 and MKS3.

TMEM107 recruits ciliopathy proteins to subdomains of the ciliary transition zone and causes Joubert syndrome.

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

Formation of the B9-domain protein complex MKS1-B9D2-B9D1 is essential as a diffusion barrier for ciliary membrane proteins.

Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.

Multimodal cell maps as a foundation for structural and functional genomics.

Functional interactions between the ciliopathy-associated Meckel syndrome 1 (MKS1) protein and two novel MKS1-related (MKSR) proteins.

Combined Automated Annotation using Multiple IEA Methods

Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara

The Ciliary Transition Zone: Finding the Pieces and Assembling the Gate.

RAB3IP stimulates nucleotide exchange on RAB8A

Recruitment of transition zone proteins

CEP164 recruits RAB3IP-carrying Golgi-derived vesicles to the basal

Electronic Gene Ontology annotations created by ARBA machine learning models

A ciliopathy complex at the transition zone protects the cilia as a privileged membrane domain.

Annotation inferences using phylogenetic trees

Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity

Gene Ontology annotation based on curation of immunofluorescence data

MKS5 and CEP290 Dependent Assembly Pathway of the Ciliary Transition Zone.