abnormal head movements Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002457
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Genes

6 genes associated with the abnormal head movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
DLAT dihydrolipoamide S-acetyltransferase
FMR1 fragile X mental retardation 1
GJC2 gap junction protein, gamma 2, 47kDa
KIF1C kinesin family member 1C
PLP1 proteolipid protein 1
UCHL1 ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase)