rotary nystagmus Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A form of nystagmus in which the eyeball makes rotary motions around the axis. (Human Phenotype Ontology, HP_0001583)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001583
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Genes

5 genes associated with the rotary nystagmus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
GJC2 gap junction protein, gamma 2, 47kDa
MPC1 mitochondrial pyruvate carrier 1
NPHP4 nephronophthisis 4
PLP1 proteolipid protein 1
SLC16A2 solute carrier family 16, member 2 (thyroid hormone transporter)