Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Expression Phenotypes Gene Literature (5) GO Terms (44) Nucleotides (44) Proteins (23) Interactants (151) Wiki
XB-GENEPAGE-957296
???displayGene.symbol???:
 ush2a

???displayGene.name???: 
Usher syndrome 2A (autosomal recessive, mild)

???displayGene.synonyms???
LOC121394161 ( Nomenclature history )

???displayGene.geneFunction???
Extracellular matrix glycoprotein Laminin subunits alpha and gamma

AI Protein Function :
The ush2a gene encodes a protein involved in cell adhesion and functions in the development of the inner ear and retina. It localizes to the photoreceptor cells.


InterPro :
ConA-like dom sf, FN3 dom, FN3 sf, Ig-like fold, [+]

???displayGene.geneInteractants???
Loading ...

Diseases: 


Disease Ontology:
retinitis pigmentosa 39 [+]

MIM:
USHER SYNDROME, TYPE IIA; USH2A [+]

External Links:
 
???displayGene.expression???                  Development Stages                                               Embryonic Tissues                                                                Adult Tissues
More Information
Xenbase Expression Details In situ images Single cell data at SPRING In situ: RNA-Seq:


Symbol legend: Blast sequence    View sequence    Literature or expression images   Hover cursor for info