Essential Tremor Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A movement disorder that causes involuntary tremors, especially in the hands. It occurs alone without other neurological signs and symptoms. (Human Disease Ontology, DOID_4990)
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21 genes/proteins associated with the disease Essential Tremor from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
LINGO1 leucine rich repeat and Ig domain containing 1 2.88009
GABRA1 gamma-aminobutyric acid (GABA) A receptor, alpha 1 2.88009
FOS FBJ murine osteosarcoma viral oncogene homolog 1.67159
TAC1 tachykinin, precursor 1 1.40288
DRD2 dopamine receptor D2 1.37987
DRD1 dopamine receptor D1 1.36648
GRIN2A glutamate receptor, ionotropic, N-methyl D-aspartate 2A 1.2772
NOS2 nitric oxide synthase 2, inducible 1.27255
PENK proenkephalin 1.23837
PRKCA protein kinase C, alpha 1.14816
GRIN2B glutamate receptor, ionotropic, N-methyl D-aspartate 2B 1.09786
GNAS GNAS complex locus 1.09262
ADORA1 adenosine A1 receptor 1.08442
HDAC3 histone deacetylase 3 1.07128
GRIN1 glutamate receptor, ionotropic, N-methyl D-aspartate 1 1.06881
PRKCG protein kinase C, gamma 1.06625
BDNF brain-derived neurotrophic factor 1.06442
ARNT aryl hydrocarbon receptor nuclear translocator 1.059
MAOA monoamine oxidase A 1.03493
GABBR1 gamma-aminobutyric acid (GABA) B receptor, 1 1.02671
GABRB1 gamma-aminobutyric acid (GABA) A receptor, beta 1 1.01928