GIGYF2 Back

GRB10 interacting GYF protein 2

External References:      Wikipedia GeneCards HUGO COSMIC Google Scholar

NCBI Description of GIGYF2
The protein encoded by this gene interacts with GRB10 and may be involved in the regulation of tyrosine kinase receptor signaling. This gene contains CAG repeats, and the encoded protein contains stretches glutamine and glutamic acid residues. Defects in this gene are a cause of Parkinson disease type 11 (PARK11). Multiple transcript variants encoding several different isoforms have been found for this gene. Sequence Note: This RefSeq record was created from transcript and genomic sequence data because no single transcript was available for the full length of the gene. The extent of this transcript is supported by transcript alignments.

Community Annotation of GIGYF2 Add / Edit GIGYF2: Annotations

No community annotations yet for GIGYF2.
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

GIGYF2 is highly significantly mutated in
(none)
GIGYF2 is significantly mutated in
(none)
GIGYF2 is near significance in
(none)

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

Data details


• Mutation list for GIGYF2