RPE65 Gene Set

Dataset Pathway Commons Protein-Protein Interactions
Category physical interactions
Type interacting protein
Description retinal pigment epithelium-specific protein 65kDa|This gene encodes a protein which is located in the retinal pigment epithelium and is involved in the production of 11-cis retinal and in visual pigment regeneration. There are two forms of this protein, a soluble form called sRPE65, and a palmitoylated, membrane-bound form known as mRPE65. mRPE65 serves as the palmitoyl donor for lecithin retinol acyl transferase (LRAT), the enzyme that catalyzes the vitamin A to all trans retinol step of the chromophore regeneration process. Both mRPE65 and sRPE65 also serve as regulatory proteins, with the ratio and concentrations of these molecules playing a role in the inhibition of 11-cis retinal synthesis. Mutations in this gene have been associated with Leber congenital amaurosis type 2 (LCA2) and retinitis pigmentosa. [provided by RefSeq, Jul 2008] (NCBI Entrez Gene Database, 6121)
External Link http://www.ncbi.nlm.nih.gov/gene/6121
Similar Terms
Downloads & Tools

Genes

4 interacting proteins for RPE65 from the Pathway Commons Protein-Protein Interactions dataset.

Symbol Name
PSMD13 proteasome (prosome, macropain) 26S subunit, non-ATPase, 13
RBP4 retinol binding protein 4, plasma
SLC27A1 solute carrier family 27 (fatty acid transporter), member 1
UBC ubiquitin C