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 ExpressionExpr. PhenotypesPheno. Gene Literature (0)Lit. (0) GO Terms (17)GO (17) Nucleotides (190)Nucl. (190) Proteins (31)Prot. (31) Interactants (60)Interact. (60) Wiki
XB-GENEPAGE-1016149
???displayGene.symbol???:
 champ1

???displayGene.name???: 
chromosome alignment maintaining phosphoprotein 1

???displayGene.synonyms???
champ , znf828 ( Nomenclature history )

???displayGene.geneFunction???
Nucleolar GTPase/ATPase p130

InterPro :
Znf C2H2 sf, Znf C2H2 type, CAMP

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

Diseases: 


Disease Ontology:
autosomal dominant intellectual developmental disorder [+]

MIM:
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, IMPAIRED LANGUAGE, AND DYSMORPHIC FE

External Links:
Loading gene data...
Please wait while we fetch the latest information
???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