kinetic tremor Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Tremor that occurs during any voluntary movement. It may include visually or non-visually guided movements. Tremor during target directed movement is called intention tremor. (Human Phenotype Ontology, HP_0030186)
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22 genes associated with the kinetic tremor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCB7 ATP-binding cassette, sub-family B (MDR/TAP), member 7
ABHD12 abhydrolase domain containing 12
ATCAY ataxia, cerebellar, Cayman type
ATP2B3 ATPase, Ca++ transporting, plasma membrane 3
ELOVL4 ELOVL fatty acid elongase 4
FAM126A family with sequence similarity 126, member A
FMR1 fragile X mental retardation 1
GJC2 gap junction protein, gamma 2, 47kDa
GSS glutathione synthetase
ITM2B integral membrane protein 2B
ITPR1 inositol 1,4,5-trisphosphate receptor, type 1
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
PLA2G6 phospholipase A2, group VI (cytosolic, calcium-independent)
PNPLA6 patatin-like phospholipase domain containing 6
POLR3B polymerase (RNA) III (DNA directed) polypeptide B
PTEN phosphatase and tensin homolog
SCARB2 scavenger receptor class B, member 2
SCP2 sterol carrier protein 2
SPTBN2 spectrin, beta, non-erythrocytic 2
TBP TATA box binding protein
TGM6 transglutaminase 6
VLDLR very low density lipoprotein receptor