Delusions Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A belief that is pathological and is held despite evidence to the contrary. (Human Phenotype Ontology, HP_0000746)
External Link https://www.disgenet.org/browser/0/1/0/C0011253
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Genes

59 genes associated with the disease Delusions in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1
AKT1 v-akt murine thymoma viral oncogene homolog 1
ALDH1L1 aldehyde dehydrogenase 1 family, member L1
APOE apolipoprotein E
APOL2 apolipoprotein L, 2
APOL4 apolipoprotein L, 4
ARSA arylsulfatase A
BCHE butyrylcholinesterase
BCL2 B-cell CLL/lymphoma 2
BDNF brain-derived neurotrophic factor
C9ORF72 chromosome 9 open reading frame 72
CCL11 chemokine (C-C motif) ligand 11
CHI3L1 chitinase 3-like 1 (cartilage glycoprotein-39)
COMT catechol-O-methyltransferase
CYP27A1 cytochrome P450, family 27, subfamily A, polypeptide 1
DAOA D-amino acid oxidase activator
DRD2 dopamine receptor D2
DRD3 dopamine receptor D3
DRD4 dopamine receptor D4
EIF2B1 eukaryotic translation initiation factor 2B, subunit 1 alpha, 26kDa
EIF2B2 eukaryotic translation initiation factor 2B, subunit 2 beta, 39kDa
EIF2B3 eukaryotic translation initiation factor 2B, subunit 3 gamma, 58kDa
EIF2B4 eukaryotic translation initiation factor 2B, subunit 4 delta, 67kDa
EIF2B5 eukaryotic translation initiation factor 2B, subunit 5 epsilon, 82kDa
GABRA1 gamma-aminobutyric acid (GABA) A receptor, alpha 1
GABRB3 gamma-aminobutyric acid (GABA) A receptor, beta 3
GBA glucosidase, beta, acid
GRIA1 glutamate receptor, ionotropic, AMPA 1
HAL histidine ammonia-lyase
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
HTR2A 5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled
HTR6 5-hydroxytryptamine (serotonin) receptor 6, G protein-coupled
IL1B interleukin 1, beta
JPH3 junctophilin 3
MAOB monoamine oxidase B
MAPT microtubule-associated protein tau
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
NDP Norrie disease (pseudoglioma)
NRG1 neuregulin 1
NRG3 neuregulin 3
P4HB prolyl 4-hydroxylase, beta polypeptide
PADI1 peptidyl arginine deiminase, type I
PAH phenylalanine hydroxylase
PDIA2 protein disulfide isomerase family A, member 2
PPP2R2B protein phosphatase 2, regulatory subunit B, beta
PRND prion protein 2 (dublet)
PRNP prion protein
PSAP prosaposin
RTN4R reticulon 4 receptor
RTN4RL1 reticulon 4 receptor-like 1
SLC25A13 solute carrier family 25 (aspartate/glutamate carrier), member 13
SLC2A2 solute carrier family 2 (facilitated glucose transporter), member 2
SLC30A3 solute carrier family 30 (zinc transporter), member 3
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4
SNCA synuclein, alpha (non A4 component of amyloid precursor)
SNCB synuclein, beta
SYN2 synapsin II
TBC1D9 TBC1 domain family, member 9 (with GRAM domain)