STARD13 Back

StAR-related lipid transfer (START) domain containing 13

External References:      Wikipedia GeneCards HUGO COSMIC Google Scholar

NCBI Description of STARD13

This gene encodes a protein which contains an N-terminal sterile alpha motif (SAM) for protein-protein interactions, followed by an ATP/GTP-binding motif, a GTPase-activating protein (GAP) domain, and a C-terminal STAR-related lipid transfer (START) domain. It may be involved in regulation of cytoskeletal reorganization, cell proliferation, and cell motility, and acts as a tumor suppressor in hepatoma cells. The gene is located in a region of chromosome 13 that is associated with loss of heterozygosity in hepatocellular carcinomas. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.

Community Annotation of STARD13 Add / Edit STARD13: Annotations

No community annotations yet for STARD13.
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

STARD13 is highly significantly mutated in
(none)
STARD13 is significantly mutated in
(none)
STARD13 is near significance in
(none)

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

Data details


Mutation list for STARD13