TDRD7 Back

tudor domain containing 7

External References:      Wikipedia GeneCards HUGO COSMIC Google Scholar

NCBI Description of TDRD7
This gene encodes a component of cytoplasmic RNA granules which are involved in determining the fate of mRNAs. Mutation in this gene has been associated with pediatric cataracts. Mutation of the similar gene in mice has been associated with cataracts, glaucoma and a block in spermatogenesis.

Community Annotation of TDRD7 Add / Edit TDRD7: Annotations

No community annotations yet for TDRD7.
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).


Legend

TDRD7 is highly significantly mutated in
(none)
TDRD7 is significantly mutated in
(none)
TDRD7 is near significance in
(none)

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

Data details


• Mutation list for TDRD7