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MKS1 GeneMeckel syndrome, type 1 The protein encoded by this gene localizes to the basal body and is required for formation of the primary cilium in ciliated epithelial cells. Mutations in this gene result in Meckel syndrome type 1 and in Bardet-Biedl syndrome type 13. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009] |
mks1 Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term mks1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
MKS1 Gene SetFrom Pathway Commons Protein-Protein Interactions interacting proteins for MKS1 from the Pathway Commons Protein-Protein Interactions dataset. |
MKS1 Gene SetFrom CM4AI KOLF21J CRISPRi Gene Perturbation Atlas genes differentially expressed following the MKS1 gene perturbation from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas. |