Perceptual Disorders Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D010468
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Genes

24 genes/proteins associated with the disease Perceptual Disorders from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
DRD2 dopamine receptor D2 1.6428
BDNF brain-derived neurotrophic factor 1.49122
CYP3A4 cytochrome P450, family 3, subfamily A, polypeptide 4 1.37789
FOS FBJ murine osteosarcoma viral oncogene homolog 1.37733
BAX BCL2-associated X protein 1.31837
COMT catechol-O-methyltransferase 1.26329
RGS4 regulator of G-protein signaling 4 1.26021
TH tyrosine hydroxylase 1.21663
PRL prolactin 1.20031
MBP myelin basic protein 1.19246
RGS2 regulator of G-protein signaling 2 1.16533
NPY neuropeptide Y 1.13793
CNR1 cannabinoid receptor 1 (brain) 1.13041
HTR2B 5-hydroxytryptamine (serotonin) receptor 2B, G protein-coupled 1.12219
EGR1 early growth response 1 1.11325
NGF nerve growth factor (beta polypeptide) 1.07553
MAP2 microtubule-associated protein 2 1.05089
ARC activity-regulated cytoskeleton-associated protein 1.04904
SOD1 superoxide dismutase 1, soluble 1.04427
SLC18A2 solute carrier family 18 (vesicular monoamine transporter), member 2 1.04314
CAT catalase 1.03789
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1 1.03009
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6 1.01966
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4 1.01212