XB-FEAT-494949: Difference between revisions
imported>Xenbase gene generator No edit summary |
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This is the community wiki page for the gene ''rac2'' 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 ''rac2'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase | ||
= nomenclature changes= | |||
08/15/2017 | |||
Human name has changed for Entrez Gene: 5880. From ras-related C3 botulinum toxin substrate 2 (rho family, small GTP binding protein Rac2) to Rac family small GTPase 2 | |||
=summary from NCBI=This gene encodes a member of the Ras superfamily of small guanosine triphosphate (GTP)-metabolizing proteins. The encoded protein localizes to the plasma membrane, where it regulates diverse processes, such as secretion, phagocytosis, and cell polarization. Activity of this protein is also involved in the generation of reactive oxygen species. Mutations in this gene are associated with neutrophil immunodeficiency syndrome. There is a pseudogene for this gene on chromosome 6. [provided by RefSeq, Jul 2013] | |||
Revision as of 08:03, 15 August 2017
rac2
This is the community wiki page for the gene rac2 please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase
nomenclature changes
08/15/2017
Human name has changed for Entrez Gene: 5880. From ras-related C3 botulinum toxin substrate 2 (rho family, small GTP binding protein Rac2) to Rac family small GTPase 2
=summary from NCBI=This gene encodes a member of the Ras superfamily of small guanosine triphosphate (GTP)-metabolizing proteins. The encoded protein localizes to the plasma membrane, where it regulates diverse processes, such as secretion, phagocytosis, and cell polarization. Activity of this protein is also involved in the generation of reactive oxygen species. Mutations in this gene are associated with neutrophil immunodeficiency syndrome. There is a pseudogene for this gene on chromosome 6. [provided by RefSeq, Jul 2013]