XB-FEAT-6258150: Difference between revisions

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=cecr1=  
=ada2=  
This is the community wiki page for the gene ''cecr1'' 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 ''ada2'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase
 
 
=nomenclature changes=
03/13/2017
 
Human symbol has changed for genepage ID: 6258150 From cecr1 to ADA2
 
undated change:
 
Human name changed from : cat eye syndrome chromosome region, candidate 1 to: adenosine deaminase 2
 
=summary=
This gene encodes a member of a subfamily of the adenosine deaminase protein family. The encoded protein is one of two adenosine deaminases found in humans, which regulate levels of the signaling molecule, adenosine. The encoded protein is secreted from monocytes undergoing differentiation and may regulate cell proliferation and differentiation. This gene may be responsible for some of the phenotypic features associated with cat eye syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]

Latest revision as of 07:26, 23 March 2017

ada2

This is the community wiki page for the gene ada2 please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase


nomenclature changes

03/13/2017

Human symbol has changed for genepage ID: 6258150 From cecr1 to ADA2

undated change:

Human name changed from : cat eye syndrome chromosome region, candidate 1 to: adenosine deaminase 2

summary

This gene encodes a member of a subfamily of the adenosine deaminase protein family. The encoded protein is one of two adenosine deaminases found in humans, which regulate levels of the signaling molecule, adenosine. The encoded protein is secreted from monocytes undergoing differentiation and may regulate cell proliferation and differentiation. This gene may be responsible for some of the phenotypic features associated with cat eye syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]