intention tremor Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A type of kinetic tremor that occurs during target directed movement is called intention tremor. That is, an oscillatory cerebellar ataxia that tends to be absent when the limbs are inactive and during the first part of voluntary movement but worsening as the movement continues and greater precision is required (e.g., in touching a target such as the patient's nose or a physician's finger). (Human Phenotype Ontology, HP_0002080)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002080
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Genes

22 genes associated with the intention 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