Name

MKS1 Gene

Meckel 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 Set

From 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 Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for MKS1 from the Pathway Commons Protein-Protein Interactions dataset.

mks1related Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term mks1related in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.