postural tremor Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A type of tremors that is triggered by holding a limb in a fixed position. (Human Phenotype Ontology, HP_0002174)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002174
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Genes

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

Symbol Name
ATXN2 ataxin 2
FGF14 fibroblast growth factor 14
FMR1 fragile X mental retardation 1
FUS FUS RNA binding protein
GCH1 GTP cyclohydrolase 1
ITPR1 inositol 1,4,5-trisphosphate receptor, type 1
KCND3 potassium channel, voltage gated Shal related subfamily D, member 3
MPZ myelin protein zero
PARK7 parkinson protein 7
PMP22 peripheral myelin protein 22
POLR3A polymerase (RNA) III (DNA directed) polypeptide A, 155kDa
PRKRA protein kinase, interferon-inducible double stranded RNA dependent activator
SCARB2 scavenger receptor class B, member 2
TPP1 tripeptidyl peptidase I
VAPB VAMP (vesicle-associated membrane protein)-associated protein B and C