Name

GP9 Gene

glycoprotein IX (platelet)

This gene encodes a small membrane glycoprotein found on the surface of human platelets. It forms a 1-to-1 noncovalent complex with glycoprotein Ib, a platelet surface membrane glycoprotein complex that functions as a receptor for von Willebrand factor. The complete receptor complex includes noncovalent association of the alpha and beta subunits with the protein encoded by this gene and platelet glycoprotein V. Defects in this gene are a cause of Bernard-Soulier syndrome, also known as giant platelet disease. These patients have unusually large platelets and have a clinical bleeding tendency. [provided by RefSeq, Oct 2008]

gp9 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term gp9 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

GP9 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for GP9 from the Pathway Commons Protein-Protein Interactions dataset.

gp96 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term gp96 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

gp91phox Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term gp91phox in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

gp91phoxnox2 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term gp91phoxnox2 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.