XB-FEAT-940701: Difference between revisions

From XenWiki
Jump to navigation Jump to search
imported>Xenbase
imported>Xenbase
 
Line 2: Line 2:
This is the community wiki page for the gene ''reep1'' 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 ''reep1'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase


=summary fro human REEP! from NCBI=
=summary fro human REEP1 from NCBI=
This gene encodes a mitochondrial protein that functions to enhance the cell surface expression of odorant receptors. Mutations in this gene cause spastic paraplegia autosomal dominant type 31, a neurodegenerative disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]
This gene encodes a mitochondrial protein that functions to enhance the cell surface expression of odorant receptors. Mutations in this gene cause spastic paraplegia autosomal dominant type 31, a neurodegenerative disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]

Latest revision as of 11:46, 15 February 2021

reep1

This is the community wiki page for the gene reep1 please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase

summary fro human REEP1 from NCBI

This gene encodes a mitochondrial protein that functions to enhance the cell surface expression of odorant receptors. Mutations in this gene cause spastic paraplegia autosomal dominant type 31, a neurodegenerative disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]