XB-FEAT-5901112: Difference between revisions

From XenWiki
Jump to navigation Jump to search
imported>Xenbase gene generator
No edit summary
 
imported>Xenbase
 
Line 1: Line 1:
=rras2=  
=rras2=  
This is the community wiki page for the gene ''rras2'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase
This is the community wiki page for the gene ''rras2'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase.
 
=nomenclature changes=
08/07/2017
Human name has changed for Entrez Gene: 22800. From related RAS viral (r-ras) oncogene homolog 2 to RAS related 2
 
=summary from NCBI=
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]

Latest revision as of 08:37, 8 August 2017

rras2

This is the community wiki page for the gene rras2 please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase.

nomenclature changes

08/07/2017 Human name has changed for Entrez Gene: 22800. From related RAS viral (r-ras) oncogene homolog 2 to RAS related 2

summary from NCBI

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]