Aliases for RBP7 Gene
External Ids for RBP7 Gene
Previous GeneCards Identifiers for RBP7 Gene
The protein encoded by this gene is a member of the cellular retinol-binding protein (CRBP) family, whose members are required for vitamin A stability and metabolism. The encoded protein binds all-trans-retinol and is structurally similar to other CRBPs; however, it has a lower binding affinity for retinol than other CRBPs. [provided by RefSeq, Aug 2016]
GeneCards Summary for RBP7 Gene
RBP7 (Retinol Binding Protein 7) is a Protein Coding gene. Diseases associated with RBP7 include Leber Congenital Amaurosis 9 and Leber Congenital Amaurosis. Among its related pathways are Vitamin A and Carotenoid Metabolism and Visual Cycle in Retinal Rods. Gene Ontology (GO) annotations related to this gene include transporter activity and retinol binding. An important paralog of this gene is RBP2.
UniProtKB/Swiss-Prot for RBP7 Gene
Intracellular transport of retinol.