We apologize for Proteopedia being slow to respond. For the past two years, a new implementation of Proteopedia has been being built. Soon, it will replace this 18-year old system. All existing content will be moved to the new system at a date that will be announced here.

CTLA-4

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 7: Line 7:
== Disease ==
== Disease ==
-
Variants in this gene have been associated with Type 1 diabetes<ref>PMID:10671941</ref>, Graves' disease, Hashimoto's thyroiditis, celiac disease, systemic lupus erythematosus, thyroid-associated orbitopathy, primary biliary cirrhosis and other autoimmune diseases.
+
Variants in this gene have been associated with Type 1 diabetes<ref>PMID:10671941</ref>, Graves' disease, Hashimoto's thyroiditis<ref>PMID:12914522</ref>, celiac disease, systemic lupus erythematosus, thyroid-associated orbitopathy, primary biliary cirrhosis and other autoimmune diseases.
== Structural highlights ==
== Structural highlights ==

Revision as of 07:57, 10 February 2021

Human glycosylated CTLA4 extracellular domain (pink) complex with CD80 (grey) (PDB code 1i8l)

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

Michal Harel, Supriya Pal Sharma, Alexander Berchansky

Personal tools