tremor by anatomical site Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Tremor classified by the affected body part. (Human Phenotype Ontology, HP_0030188)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0030188
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Genes

19 genes associated with the tremor by anatomical site phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ANO3 anoctamin 3
CDKL5 cyclin-dependent kinase-like 5
FGF14 fibroblast growth factor 14
GBA2 glucosidase, beta (bile acid) 2
GJC2 gap junction protein, gamma 2, 47kDa
KIF1C kinesin family member 1C
MECP2 methyl CpG binding protein 2
MPZ myelin protein zero
PDK3 pyruvate dehydrogenase kinase, isozyme 3
PLP1 proteolipid protein 1
PMP22 peripheral myelin protein 22
PPP2R2B protein phosphatase 2, regulatory subunit B, beta
SCP2 sterol carrier protein 2
SETX senataxin
SLC12A6 solute carrier family 12 (potassium/chloride transporter), member 6
SMN1 survival of motor neuron 1, telomeric
TFG TRK-fused gene
UBE3A ubiquitin protein ligase E3A
UCHL1 ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase)