Aliases for RRAS2 Gene
External Ids for RRAS2 Gene
Previous GeneCards Identifiers for RRAS2 Gene
This gene encodes a member of the R-Ras subfamily of Ras-like small GTPases. The encoded protein associates with the plasma membrane and may function as a signal transducer. This protein may play an important role in activating signal transduction pathways that control cell proliferation. Mutations in this gene are associated with the growth of certain tumors. Pseudogenes of this gene are found on chromosomes 1 and 2. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Apr 2010]
GeneCards Summary for RRAS2 Gene
RRAS2 (RAS Related 2) is a Protein Coding gene. Diseases associated with RRAS2 include Noonan Syndrome 12 and Noonan Syndrome 1. Among its related pathways are Apelin signaling pathway and G-Beta Gamma Signaling. Gene Ontology (GO) annotations related to this gene include GTP binding and GTPase activity. An important paralog of this gene is RRAS.
UniProtKB/Swiss-Prot Summary for RRAS2 Gene
GTP-binding protein with GTPase activity involved in the regulation of MAPK signaling pathway, thereby controlling multiple cellular processes (PubMed:31130282). Involved in the regulation of MAPK signaling pathway (PubMed:31130282, PubMed:31130285). Regulation of craniofacial development (PubMed:31130282, PubMed:31130285).