LRRC6 Back

leucine rich repeat containing 6

External References:      Wikipedia GeneCards HUGO COSMIC Google Scholar

NCBI Description of LRRC6

The protein encoded by this gene contains several leucine-rich repeat domains and appears to be involved in the motility of cilia. Defects in this gene are a cause of primary ciliary dyskinesia-19 (CILD19). Two transcript variants, one protein-coding and the other not, have been found for this gene.

Community Annotation of LRRC6 Add / Edit LRRC6: Annotations

No community annotations yet for LRRC6.
Sort mutations by: Tumor type  Mutation type  Position  
Straightedge cursor Expand

Figure notes

• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


LRRC6 is highly significantly mutated in
LRRC6 is significantly mutated in
LRRC6 is near significance in

Click on a tumor type to see its full list of significant genes.

Data details

Mutation list for LRRC6