Name

CC2D2A Gene

coiled-coil and C2 domain containing 2A

This gene encodes a coiled-coil and calcium binding domain protein that appears to play a critical role in cilia formation. Mutations in this gene cause Meckel syndrome type 6, as well as Joubert syndrome type 9. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]

cc2d2a Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term cc2d2a in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

CC2D2A Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for CC2D2A from the Pathway Commons Protein-Protein Interactions dataset.

CC2D2A Gene Set

From LINCS L1000 CMAP CRISPR Knockout Consensus Signatures

genes differentially expressed following the CC2D2A gene perturbation from the LINCS L1000 CMAP CRISPR Knockout Consensus Signatures dataset.

CC2D2A, N-terminal, C2 domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the CC2D2A, N-terminal, C2 domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.