abnormality of the dentate nucleus Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the dentate nucleus. (Human Phenotype Ontology, HP_0100321)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100321
Similar Terms
Downloads & Tools


4 genes associated with the abnormality of the dentate nucleus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATN1 atrophin 1
CYP27A1 cytochrome P450, family 27, subfamily A, polypeptide 1
SLC20A2 solute carrier family 20 (phosphate transporter), member 2
WDR81 WD repeat domain 81