SLCO1A2 Back

solute carrier organic anion transporter family, member 1A2

External References:      Wikipedia GeneCards HUGO COSMIC Google Scholar

NCBI Description of SLCO1A2

This gene encodes a sodium-independent transporter which mediates cellular uptake of organic ions in the liver. Its substrates include bile acids, bromosulphophthalein, and some steroidal compounds. The protein is a member of the SLC21A family of solute carriers. Alternative splicing of this gene results in multiple transcript variants.

Community Annotation of SLCO1A2 Add / Edit SLCO1A2: Annotations

No community annotations yet for SLCO1A2.
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

SLCO1A2 is highly significantly mutated in
(none)
SLCO1A2 is significantly mutated in
(none)
SLCO1A2 is near significance in
(none)

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

Data details


Mutation list for SLCO1A2