Schizophrenia

About the Disease
Schizophrenia, also known as schizophrenia with or without an affective disorder, is related to schizoaffective disorder and psychotic disorder, and has symptoms including sleep disturbances, photophobia and personality changes. An important gene associated with Schizophrenia is RTN4R (Reticulon 4 Receptor), and among its related pathways/superpathways are "Methylphenidate Pathway, Pharmacodynamics" and MTHFR deficiency. The drugs Molindone and Asenapine have been mentioned in the context of this disorder. Affiliated tissues include brain, prefrontal cortex and cortex, and related phenotypes are eeg abnormality and hallucinations

Common Targets
UNC13B | Phosphodiesterase (nonspecified subtype) | ATF6B | MACROD2 | FASTKD3 | NRXN3 | ZNF536 | ZKSCAN4 | HCG17 | MIR2682 | ADAM10 | ADCY10 | SORBS1 | HLA-DQB1 | SCN5A | SELE | MMP16 | RASA3 | MLXIP | MSL2 | TEKT5 | ABCA13 | MRPL41 | Glutamate Receptor Ionotropic AMPA Receptor | MPO | SEMA3D | RAB6B | GABBR1 | SLC39A8 | ERCC5 | CAT | MIR1976 | SELENOH | HTR7 | CYBA | ZNF791 | NFKB1 | NTRK2 | PDE4D | CACNA1H | HDAC2-AS2 | EIF4E3 | CIP2A | HTR3A | DDC | NT5C2 | CPVL | DEF8 | SPATA7 | CLSTN3 | RSPH4A | NUCKS1 | TRPC4 | SLX4 | HRH3 | ZNF488 | GPR139 | G3576 | SCN2A | KCNH2 | LAMA5 | CALHM1 | DYM | KANSL1 | KDM5B | SLC12A2 | DST | KLHL31 | CHRNB3 | CYP3A4 | SPAG17 | HROB | EPM2A | LRRTM4 | Serine/threonine-protein kinase (PAK) (nonspecified subtype) | ATXN7 | MIR137HG | UFD1 | CRELD2 | ADCYAP1 | CDK4/Cyclin D1 | ITIH1 | SMARCA1 | DPYD | TCF3 | TLR5 | COX2 | FXYD1 | LINC02267 | HEXIM1 | IL1B | ANTKMT | LDLR | CACNA1B | FAM184A | KRTAP13-4 | LINC02542 | DSE | KIF13A | 5-Hydroxytryptamine Receptor 3 (5-HT3 receptor) (nonspecified subtype) | BEND4 | NRIP1 | PRKAR1A | TRAF3IP2-AS1 | MEGF11 | LSM14A | GPR88 | HRG | RPTOR | SPOPL | SHANK3 | H3-3B | CACNA2D1 | COL18A1 | CYTH4 | SEMA5A | MALT1 | SPINK5 | ITGA1 | CDH13 | POLDIP2 | NCAN | ZEB1 | MMP17 | MINK1 | GNAL | CACNA2D2 | CFB | SCN10A | KCNC1 | TTR | FAM162B | SLC9C1 | SERPINA3 | G3569 | G6774 | DIO2 | MIR943 | GPR35 | SP4 | TACR3 | MYO7B | C1orf50 | RPGRIP1L | PRRT1 | RNR2 | VASP | IL23A | LOC105375451 | CEP85L | MAD1L1 | PREP | ADAMTSL3 | TACR2 | CRTC2 | NINL | PLEKHO2 | TTC12 | GRB10 | SLC17A6 | DENND4B | NGFR | AVPR1A | BDNF | gamma-Secretase | EEF2KMT | TBC1D32 | RBFOX1 | HPS4 | RBKS | SAMD12 | TFRC | LINC01239 | PCM1 | WDR83 | LAX1 | RALGPS1 | FAM30A | PTPRD | ITPR3 | G4089 | LYRM9 | PPA2 | TRIM15 | AMBRA1 | CA10 | STIP1 | Metabotropic glutamate (mGluR) receptor (nonspecified subtype) | TBX1 | HHAT | CKB | IL1RN | C9orf50 | SLC18A2 | DAB1 | TNRC6A | MAP2K7 | MED27 | CHRNB4 | Serine/Threonine Kinase (nonspecified subtype) | PAH | PCCB | HDAC6 | GRIK1 | GRM5 | HLA-DMB | Rho GTPase (nonspecified subtype) | LRRK2 | KCNN3 | SMG6 | KCNQ4 | GRIN2C | NCOA2 | HDAC2 | NCOR2 | ESPNL | MSX1 | EPN2 | TNPO2 | CASKIN1 | ITIH3 | IL1RAPL1 | CFI | L-type voltage-dependent calcium channel complex | VPS52 | ST3GAL3 | CNTN2 | DAO | BMAL1 | ADGRF4 | CTNNA3 | Tachykinin Receptor (nonspecified subtype) | G3620 | TTC7B | ELOB | C9orf72 | GPSM1 | GRIN1 | PSMD3 | TBC1D22A | SRR | DNMT3L | VN1R1 | CHRM4 | CEACAM16 | CLSTN2 | Phosphodiesterase IV (PDE4) (nonspecified subtype) | SMARCA2 | MTNR1A | NOS1 | PDE4B | LOC105370878 | Phosphodiesterase 1 (PDE1) (nonspecified subtype) | CYP2D6 | OPRK1 | BCL11A | CCND2 | AMP-activated protein kinase (AMPK) | CYP2C19 | AHCY | GLRA4 | SF3B3 | DHX16 | NAXD | GPR52 | NOS1AP | G595 | PLA2G4A | MRPS18B | PTPRCAP | DNMT3A | DPYSL2 | FH | AMACR | SLC7A6 | PCDHA9 | Gamma-Aminobutyric acid type B receptor | HSD17B4 | NR3C2 | DAOA | IL6-AS1 | ADRA1A | NPSR1 | ARRB2 | ADARB2 | HAGH | PRRG2 | TSPAN9 | LBX1-AS1 | ZNF169 | FAT1 | CNPPD1 | S100A16 | VPS16 | ADRA2B | TSPAN8 | COBLL1 | YWHAE | LOC105373605 | PTPRZ1 | DPYSL3 | DRD4 | NCAM1 | GNB3 | FAM177A1 | KALRN | EDEM2 | TXNRD2 | ANXA11 | PDCD11 | FLG | OPRM1 | FZD3 | YEATS2 | IFI16 | SCN3A | TGFB1 | SLC39A11 | KDM4C | ASMER1 | LIMK2 | MIR137 | PCSK5 | GRIA1 | GALNT10 | AKAP6 | NF-kappaB (NFkB) | MB | IFT74 | SSH2 | CSPG4 | SBNO1 | DNAJA3 | IL19 | CNR2 | EPHX2 | G207 | ITGA8 | NAT2 | RAD9A | HAO2 | ABCB6 | AVPR1B | KIAA1549 | FAN1 | NRG1 | IL10RA | ITGA2B | KCNQ3 | DCUN1D2 | T-Type Calcium Channel | KIT | Protein kinase C (nonspecified subtype) | LTA | G7099 | SHANK2 | ALOX12 | IMMP2L | LOC105373657 | CARNS1 | IPO11 | CNTNAP5 | ITIH4 | Alpha-2 Adrenergic receptors (nonspecified subtype) | CCDC192 | CHMP6 | GULP1 | SESN2 | SEC23IP | IL3 | SCD | CSF1R | EGR1 | YWHAG | CA12 | MGRN1 | GABRB2 | SIGMAR1 | ZNF530 | G598 | ASAH1 | UBE2E2 | POLE | GRM6 | LOC105373659 | SGK1 | CTNNA2 | KCNC2 | LAG3 | TCF20 | WDR37 | PAPSS1 | ESAM | ZEB2 | IRF3 | ACE | TSNAX-DISC1 | NRAV | EHD4 | HLA-DQA1 | FES | COLGALT1 | PDE1C | GABRG2 | HDAC5 | DROSHA | TMOD2 | KIDINS220 | SEPTIN10 | GALNTL6 | FAM178B | PPARA | BBX | CHRM1 | LIN28B | ND1 | TNIK | GEMIN4 | BAK1 | APRG1 | Small Conductance Calcium-Activated Potassium Channel (SK) (nonspecified subtype) | EFCAB6 | SPARCL1 | TUBGCP6 | FRY | CDK4 | PRORP | Lipoxygenase (nonspecified subtype) | DLG1 | MECP2 | TRPM1 | MSH5 | YWHAH | NDUFS1 | DAOA-AS1 | CDKAL1 | ADCK1 | AFG1L | MIR29B2CHG | MAGOH | ANKK1 | GRIK2 | LRRC4B | MAOA | MC2R | CYTB | AGMAT | DISC1 | SORCS3 | CACNB2 | MIR124-2HG | CACNA1G | GUCY1A2 | PRRT2 | PTPRG | GRIN2D | ABCG1 | NCAPD2 | HTR4 | KCNK2 | FBN2 | NAPEPLD | TTYH3 | HLA-B | SCN8A | KIF21B | S1PR4 | GRIA2 | HCRTR1 | SYNPO | DBH | SPATA5 | ARRB1 | GREB1L | TAAR6 | KTN1 | ARL3 | TCF4 | TCP1 | RERE | PIK3CB | IRS4 | LOC101929174 | GRM2 | ZNF101 | UQCR11 | RBM25 | MAPK12 | PRDM14 | LINC00320 | CAMKV | TRPM8 | MAP2K1 | NRG3 | S100A2 | NFATC2 | BTG2 | TMTC1 | FBH1 | CNTN6 | PDE10A | NRM | SNRPN | DRD5 | SLC39A12 | RASD1 | NGEF | DNAJC15 | DLC1 | FAT3 | EML6 | ESR2 | NUDT16L1 | PIK3R1 | ZNF638 | NXPH1 | HMGCR | NR4A1 | EGR2 | PDE9A | LSM1 | IL6R-AS1 | LOC105377941 | Glutamate Transporter (nonspecified subtype) | NOD2 | SLC4A11 | HLA-DRB1 | NLGN4X | G1385 | alpha-Secretase (nonspecified subtype) | C16orf89 | UPF3B | NOTCH4 | HDAC11 | PLAGL1 | PPP2R2B | BTNL2 | ARHGEF19 | S100A3 | KRT7 | SV2C | PSD3 | PIK3CD | CD48 | MDC1 | PTPN21 | Neurotrophic Factor (nonspecified subtype) | Nicotinic alpha3beta4 Receptor | DRD2 | ZBTB42 | TRANK1 | XIAP | CACNG8 | COMT | alpha-Adrenoceptor (nonspecified subtype) | HOXB-AS3 | MBD3 | FXYD6 | HTR2B | SLC6A2 | SLC6A9 | CFAP53 | FXYD5 | LEP | CALY | CD244 | LOC100128966 | LOC100287329 | SFTPC | DLG2 | MICB | FBXO15 | NPY2R | FLRT1 | CAST | GFRA1 | FAM86B3P | XPR1 | HTR1A | POLD4 | Opioid receptor (nonspecified subtype) | Acetylcholine Receptors (Nicotinic) (nAChR) (nonspecified subtype) | MBD1 | CSPG5 | PTGIS | TIAM1 | GID4 | OGG1 | SLC4A10 | ZBTB40 | CNR1 | RPS6KB2 | MEF2C | OR1A2 | FGA | NTSR2 | FOXP1 | ADSS1 | MGAT5B | CACNA1C | LSAMP | ND2 | NRN1 | LARP7 | HDAC3 | S100A14 | S100A4 | BNIP3 | MTRR | H2BC21 | GRIA3 | AVEN | RNF144A | ZFAT | UPP2 | BEND7 | TRPV2 | HTR5A | Nicotinic alpha4beta2 receptor | PCDH15 | PDGFRB | GLO1 | GRM7 | LOC105369603 | CHRNA7 | FHIT | CA7 | SLC44A4 | PIPOX | RSPH3 | HAO2-IT1 | PLXNC1 | LINC01414 | PCNX1 | GABRG3 | LOC105375951 | BCHE | RTN1 | S100A5 | UBQLNL | GABA(A) receptor | RETREG2 | BRD1 | MIGA2 | MASP2 | ZNF516 | C12orf54 | CALN1 | DGCR8 | UTS2R | NSD3 | SNTA1 | TGM2 | TBL1XR1 | HIBCH | ANGPT2 | LOC105374193 | MTNR1B | GFRA2 | GPX1 | BTN3A2 | KLHL1 | SOD2 | Arrestin (nonspecified subtype) | PPP1CA | PRODH | Histone acetyltransferase (HAT) (nonspecified subtype) | ABCC2 | S100A6 | KCNC3 | TCN1 | S1PR3 | NBPF3 | AAK1 | FXYD2 | NTRK3 | OLA1 | HDAC1 | HSD11B1 | CCL11 | DNMT3B | NRGN | CAMK2A | CASP4 | LOC105376107 | HLA-DRA | ADRA2A | KCNJ3 | EIF5 | LOC100507053 | C4BPB | FUCA1 | GRIA4 | TRPV1 | SEMA4B | MAP4K4 | LOC107984113 | APBA2 | KIF17 | LIN7B | KCNQ Channels (K(v) 7) (nonspecified subtype) | HTR3C | MPG | SMARCA5 | EPC2 | CBFA2T3 | BORCS7-ASMT | ZSCAN2 | CNTF | LILRB3 | SHISA9 | RAB11FIP1 | LINC02038 | ZBED4 | LOC652276 | CMYA5 | H1-0 | CDK6/Cyclin D1 | ARVCF | TMX2-CTNND1 | GFRA3 | TRAPPC3 | QPCTL | OLIG2 | CREB3L1 | ZDHHC8 | CES1 | STAT5 (nonspecified subtype) | Orexin receptor (nonspecified subtype) | FKBP5 | ORC5 | PPARG | G3605 | DLG4 | ADGRV1 | MEF2C-AS1 | RB1CC1 | PTGS1 | MAP4K1 | AGXT2 | SLC6A11 | PI4KA | CSMD1 | PPP1R13B | TREM2 | PRF1 | ZNF804A | SLC19A1 | TRIM26 | CYFIP1 | PLG | C1orf167 | HLA-A | DHPS | EMX1 | NPY | RELL2 | PTPN1 | EBF1 | ND3 | TTC39A | G2309 | PEAK1 | Voltage-Gated Sodium Channel Complex | SSTR4 | F2 | NPY5R | OXT | QPCT | NBEA | PTPRA | NTRK1 | GABRB3 | LOC100287944 | GRIK3 | GRIN2A | GRM8 | GSK3B | BUB1B-PAK6 | WDR3 | IL11RA | TSPO | PTPN5 | PLAT | PCLO | PRL | ACHE | SERPINE1 | BACE1 | CDH7 | SLC17A9 | NMBR | PKDCC | ARHGEF11 | STT3A | DNAH2 | FBXO41 | TRPC6 | CXXC4-AS1 | CCDC137 | MTHFD1 | OPRD1 | CUL3 | MS4A1 | PHACTR3 | COL4A2 | CTNND1 | FRMD5 | ACP3 | GSTT1 | EYS | KRT40 | SLC23A3 | XRCC3 | RHPN2 | FANCI | CD7 | MAPK4 | OR52B6 | TNR | IFI44 | TLR2 | IGSF9B | GABRA1 | RNF186 | ANKS3 | Triacylglycerol Lipase (TG Lipase) (nonspecified subtype) | VIPR2 | NFKBIL1 | LOC105374456 | HCRTR2 | PTGDR2 | RBP1 | LIPC | ELAVL4 | DICER1 | LOC105378340 | G9734 | sigma Receptor (nonspecified subtype) | AXDND1 | ARHGAP10 | TASOR | FAHD1 | COA8 | NDE1 | OSBPL10 | ATP2A2 | HERC1 | ENOX1 | NRXN1 | BCL9 | LRP1 | ALS2CL | LINC01470 | NEURL1 | GABBR2 | CHRM3 | SLC25A10 | SPG7 | DRD1 | RGS6 | BDNF-AS | FOLH1 | PDE4C | LINC01362 | SAR1A | TPH2 | UHMK1 | RP1 | PJA1 | Glycogen synthase kinase 3 (GSK-3) (nonspecified subtype) | G7157 | ATP1A3 | NTNG1 | DTNBP1 | GPR151 | NDUFS7 | G6PC1 | KDM2B | TGM5 | LOC105378502 | ERCC2 | IL18RAP | LOC105374524 | ANKS1B | HSPB1 | FTCDNL1 | NTSR1 | DGKD | GRID2 | CALCRL | ST8SIA5 | CHN1 | WDR53 | PDE1B | MIR34AHG | CCL17 | TRPV3 | SRPK2 | SIN3B | ZDHHC2 | MICB-DT | OGA | NLRC4 | BNIP3L | EPOR | G2099 | KCNH3 | LOC101927164 | LINC01317 | KCNQ5 | ADCYAP1R1 | ADH7 | FAAH | KDM1A | ALPK3 | CHRNA3 | CLCN3 | CRYGD | G836 | GABRR2 | SLC36A3 | LOC102725148 | IL1RAP | PEPD | MIR4507 | LINC01727 | NEUROD4 | BHLHE23 | BCL11B | Glycine receptor | DENND5B | NSD2 | SLC11A2 | SCARA3 | HTR3B | ACSM1 | DOCK3 | MMP13 | ND4 | LINC01539 | LIME1 | VPS45 | ADRA1D | CYP1A2 | Sodium channel (nonspecified subtype) | CYP3A5 | LAMA2 | GRM3 | EP400 | CYP3A43 | HSP90AB4P | LOXL2 | G4318 | ZNF365 | PREX2 | SDF4 | GPM6A | CHMP7 | FUT9 | SNAP91 | Dopamine receptor (nonspecified subtype) | SLC1A1 | PDE2A | OR8B8 | DLX5 | HIP1R | SMPD3 | ST6GALNAC1 | GMEB1 | MPDU1 | CYGB | LINC03035 | CHI3L1 | SNAP25 | LIF | TLL1 | THAP8 | BPNT2 | HOXB6 | MAN1A1 | MDN1 | NR3C1 | KLHL2 | MAPKAPK3 | RPF1 | NGFR-AS1 | LOC107984782 | PROKR1 | HSPA1A | RORB | RYR3 | AGA | USH2A | DDR1 | LAMA1 | PPP1R10 | GRAMD1B | SCN1A | TPH1 | TSNAX | S1PR5 | APEX1 | AP-1 Transcription Factor Complex | PACRG | SLC36A2 | EP300-AS1 | HTR6 | KCNMA1 | L-Type calcium channel (nonspecified subtype) | TXNRD1 | PTN | RAB3IL1 | SP7 | Poly [ADP-ribose] polymerase (nonspecified subtype) | Tubulin | LINC02232 | CABIN1 | TRERF1 | IRF6 | FAM120A | LMAN2L | LINC00624 | TMEM97 | GRM1 | PERP | FNDC4 | GABRA5 | GABRD | TMEM176A | IFNAR1 | IL1A | ZNF565 | SLC6A1 | PDE7B | CWC22 | CHRM5 | CNTN4 | AFF3 | SYN2 | NQO2 | FAM186B | SETD1A | AS3MT | GM2A | IL2 | ZNF664 | CA2 | BLTP3A | TENM3 | ADAMTS3 | CHL1 | MSI2 | ATP6 | PAK1 | SIN3A | IDH3B | EME1 | MIGA1 | FAM53C | TRMT2A | ADAM7 | SPHK1 | FOXH1 | GSN | SDCCAG8 | SLC26A8 | BORCS5 | RFX4 | FBXO16 | NFYC | ATAT1 | THAP1 | LINC01748 | CA9 | GSE1 | SPATS2L | SNX29 | IGF2BP3 | SCN9A | 5-Hydroxytryptamine Receptor 2 (5-HT2) (nonspecified subtype) | MSR1 | LOC105378793 | MAN2A1 | TRIO | VRK2 | FURIN | NUP160 | MAU2 | PRR12 | DGCR2 | ZSWIM6 | KPNA1 | EML5 | FGF13 | CACNA1A | MIR4538 | PYGO2 | C3orf14 | KLF6 | PDE4A | PPP1R16B | DCHS2 | LOC107984934 | HTR1B | SKOR2 | SLC6A4 | TH | MMP8 | DAGLA | GPC6 | STAG1 | ASIC1 | ASB2 | PGBD1 | GNG2 | PBRM1 | CHD4 | TBC1D10C | Muscarinic Acetylcholine Receptor (mAChR) (nonspecified subtype) | Gastric H+/K+-ATPase | STX1A | AGO4 | DGKI | MAP2K2 | HRH1 | IL21 | CD109 | ERBB4 | PDE5A | MASP1 | DHX33 | KIAA0513 | ARID4A | SOX10 | G4233 | MMP2 | STON2 | AMH | HSPE1-MOB4 | CORO1B | CTLA4 | LASP1 | G1786 | TACR1 | MAN2B1 | FANCA | G5743 | BTBD9 | SGCZ | NPAS3 | CPEB1 | alpha1-Adrenoceptor (nonspecified subtype) | LIPE | ZMYM6 | Histamine Receptor (HR) (nonspecified subtype) | LIG1 | LINC02694 | GRAMD2A | PALS2 | GABRA2 | IL18R1 | WSCD2 | LAMA3 | PPP1R18 | LRP2 | G7124 | SDK1 | SYNE1 | PPP3R1 | LOC105378800 | GIPC1 | NECTIN2 | NMDA receptor | MIAT | R3HDM2 | GAD1 | SLC39A13 | RMND5B | UTRN | PROX1 | C3 | TYROBP | TTLL12 | SH2B3 | MIR4539 | PRSS16 | C4BPA | ARHGAP18 | HNF4A | MCM7 | SLITRK3 | MAPKBP1 | NT5E | SATB2 | CLCF1 | KAT5 | SDC3 | Imidazoline I2 receptor (I2) | ITGAL | SLC7A4 | NR4A2 | FLT3 | MINDY4 | LRP1B | GARRE1 | G367 | LRFN3 | PIP4K2A | NCAPG2 | ADCY1 | CPXM2 | MSRA | KCNB2 | IFNG | FMO3 | CFH | HCAR2 | 5-Hydroxytryptamine Receptor (nonspecified subtype) | ROBO1 | GNB1L | SLU7 | HTR3D | NDUFA6 | KCNN1 | CNKSR2 | LRP8 | P2RX7 | PCNT | PRSS12 | CACNA1I | GPHN | DONSON | CD28 | HTR2A | ARC | FRAS1 | TRPA1 | ANK3 | GRM4 | CDC42 | ABCA2 | HCN1 | ND5 | CUL9 | VSIG2 | FYN | WDFY4 | ANKRD45 | DEGS2 | CSF2RB | ADRA1B | EGR3 | LCTL | MIF | TM4SF20 | PHF2P1 | AKT3 | RNF11 | PROX1-AS1 | MSH5-SAPCD1 | PAK4 | IGF2BP2 | STAG3 | SLC17A7 | HSPA1L | ARHGAP4 | NQO1 | MIR29B2 | FBXO45 | GNMT | CREBBP | MMP14 | THOC7 | H2AZ1 | ESYT2 | SLC30A8 | SLC30A1 | G5243 | WBP1L | FCHSD1 | MIR6165 | SLC7A10 | Neuronal acetylcholine receptor alpha2beta2 receptor | NNMT | NEK11 | GABRA6 | FBXW9 | PKD2L1 | GSTM1 | DDX55 | HTR2C | RGS2 | IL10 | ABAT | SIRT3 | CSMD2 | Glutamate Receptor Ionotropic (nonspecified subtype) | GRIN3A | CCL2 | CCDC60 | DCUN1D4 | OPCML | ANKRD27 | NEGR1 | LINC01088 | KLF12 | BARD1 | RAP1GAP | MTHFR | DAGLB | HELZ2 | LETM2 | SLC29A1 | PDE1A | LOC102723536 | PCDHAC1 | MRTFA | DAXX | Potassium Channels (nonspecified subtype) | CCZ1B | PLA2G12A | GAP43 | DYNLL1 | MBD2 | ALG1 | MBD6 | SNORC | DHFR | EPHA8 | DNAJB11 | KCNG2 | MYO1H | MCHR1 | CRP | NFASC | PRKCE | CHRNB2 | IL6R | Nicotinic alpha3beta2beta3 receptor | Histone deacetylase (nonspecified subtype) | G2146 | NEK1 | FOS | ARID1A | GPR17 | IL4 | TAAR1 | LINC00461 | DRD3 | S1PR1 | EFNA5 | NVL | KREMEN1 | NALCN | AGO1 | CNNM2 | LOC102723686 | DLGAP2 | TAOK2 | NUP50 | HRH4 | TXK | NLGN1 | ALOX5 | MDGA1 | PPEF2 | LOC105375032 | MTR | PRKN | PRKG1 | PPARGC1A | SCAF1 | CKM | FREM2 | CDH23 | LOC105375033 | RGS4 | SLC1A2 | SLC8A1 | TAP2 | NKAPL | BRAP | GRK6 | PCDHA13 | GRIN3B | GALNT15 | APOE | TSPAN18 | CD68 | ATXN2 | CERK | SRRD | PCGF3 | PAK6 | MAOB | NALF1 | G238 | GABRG1 | MPHOSPH9 | TSNARE1 | SLC6A5 | LIPG | CAMKK2 | CHRM2 | KCNN2 | MIR29C | WDR25 | AP3B2 | HOTAIR | PTAFR | ITPR1 | GAD2 | LOC105379174 | RAPSN | SLC6A3 | EFNB2 | G7422 | GPR143 | TREML2 | H19 | RELN | CLOCK | PTGER2 | CHRNA1 | Soluble guanylyl cyclase | RENBP | SLC9B1 | KDR | DNAH9 | MIR219A1 | OXTR | GABRA3 | BANK1 | ZNF823 | GSTP1 | NEBL | LOC105375056 | ADH1C | KCNB1 | GPR161 | DMTF1 | EXOC4 | RPS6KA1 | ATP2B2 | CAPN2 | SCAF11 | GPR55 | CHRNA5 | AADAT | GIGYF2 | AGBL4 | MIR4761 | ESPNP | DHX37 | SOX2-OT | XKR3 | NGF | GABRB1 | MPC2 | DKK2 | NOL4 | KAT2B | SPECC1 | TACC2 | HLA-C | RAD51B | G596 | IL18 | KCND2 | HCG23 | PLEKHA6 | GRIN2B | MAGI2 | KCNQ2 | CDK19 | CTBP2 | NCF1 | DCC | WWC1 | EDIL3 | MYLIP | TBC1D15 | ADRA2C | XRCC1 | AIG1 | AHI1 | GRIK4 | LRRTM1 | EPHB1 | C8A | NSRP1 | KMO | GSK3A | SV2A | NKAIN2 | TCF7L2 | G1956 | XBP1 | MIR4537 | LOC102723906 | RASSF1 | DVL2 | CASZ1 | LOC105379382 | PDLIM5 | FBXL21P

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Tonsillitis | Acne Vulgaris | Poretti-Boltshauser Syndrome | Anti-glomerular Basement Membrane Disease | Imerslund-Grasbeck Syndrome | Dengue Hemorrhagic Fever | Sleep Disorder | Porokeratosis | Mixed Connective Tissue Disease | Mitochondrial DNA Depletion Syndrome 13 | Hydronephrosis | Overactive Bladder | Lipid Metabolism Disorders | Marfan Syndrome | Enlarged Vestibular Aqueduct | Jaundice, Obstructive | Gastroschisis | Aldosterone Deficiency | HIBCH Deficiency | Cholangitis | Pseudohypoparathyroidism Type 1B | Schizotypal Personality Disorder | Echinococcosis | Distal Myopathy | Primary Cutaneous Amyloidosis | Osteitis | Fibrosarcoma | Inflammatory Bowel Disease | Congenital Mirror Movements | Rothmund-Thomson Syndrome | Lichen Planus | Macular Corneal Dystrophy | Brugada Syndrome 1 | Schamberg Disease | Kaposiform Hemangioendothelioma | Aldosterone Synthase Deficiency | Myoclonus | Peeling Skin Syndrome Type B | Tinea Versicolor | Pemphigus Vulgaris | Hypercholesterolemia, Familial | Dyslipidemia | Malignant Fibrous Histiocytoma | Kabuki Syndrome 2 | Cystitis | Plasma Cell Dyscrasia | Brachydactyly | Waardenburg Syndrome Type 4A | Hemochromatosis Type 2 | Adenocarcinoma | Bronchiectasis | Behcet's Disease | Chronic Thromboembolic Pulmonary Hypertension | T-cell Prolymphocytic Leukemia | Endophthalmitis | Familial Mediterranean Fever | Snyder-Robinson Syndrome | Meckel-Gruber Syndrome | Glaucoma, Congenital | Atrial Septal Defect | Hyperoxaluria | Inflammatory Myopathy | Trachoma | Parkinsonism | Cervicitis | Cancer, Colon | Oculodentodigital Dysplasia | Teratozoospermia | Giant Cell Arteritis | Glycogen Storage Disease Type 5 | Spinocerebellar Ataxia Type 20 | Heterotaxy | Progressive Encephalopathy-optic Atrophy Syndrome | Hypertelorism | Niemann-Pick Disease, Type B | Autoimmune Polyendocrine Syndrome | Double Outlet Right Ventricle | Intestinal Hypomagnesemia 1 | Osteoarthritis | Schwannomatosis | Small Lymphocytic Lymphoma | Glycogen Storage Disease Type 3 | Greenberg Dysplasia | Primary Hyperoxaluria | Behavioral Variant Of Frontotemporal Dementia | Long QT Syndrome Type 3 | Tularemia | Angina Pectoris | Granuloma Annulare | Pterygium | Rhabdomyosarcoma, Embryonal | Encephalopathy, Ethylmalonic | Uremic Pruritus | Corticobasal Syndrome | Spinocerebellar Ataxia Type 16 | Persistent Mullerian Duct Syndrome | Chorea | Fetal Alcohol Syndrome | Pulmonary Stenosis | Hyperinsulinemic Hypoglycemia | Jawad Syndrome | Rickets | Spinocerebellar Ataxia Type 23 | Seminoma | Renpenning Syndrome | Adenoma, Villous | Bone Giant Cell Tumor | CHOPS Syndrome | Roberts Syndrome | Pericarditis | Pantothenate Kinase-associated Neurodegeneration | Lichen Sclerosus | Large Granular Lymphocytic Leukemia | Alpha-1 Antitrypsin Deficiency | Kernicterus | Asplenia | Macrophage Activation Syndrome | Chondrodysplasia Punctata 1, X-linked Recessive | Triple A Syndrome | Spinocerebellar Ataxia Type 5 | Epidermolytic Hyperkeratosis | Glycogen Storage Disease Type 6 | Corneal Dystrophy And Perceptive Deafness | WAGR Syndrome | Mucolipidosis Type III | Alopecia Totalis | Myositis | Asphyxia Neonatorum | Apraxia | Obesity | Isobutyryl-CoA Dehydrogenase Deficiency | Agoraphobia | Blepharospasm | Colitis | Dubin-Johnson Syndrome | Tetanus | Fibronectin Glomerulopathy | Axenfeld-Rieger Syndrome | Tracheal Disorders | Hypersomnia | Epidermal Nevus Syndrome | Adams-Oliver Syndrome | Huntington's Disease-like 2 | Eosinophilia | Postpartum Depression | Papilloma | Spinocerebellar Ataxia Type 38 | Leber Congenital Amaurosis | Thanatophoric Dysplasia Type 1 | Spinal Muscular Atrophy Type 2 | Supravalvular Aortic Stenosis | Hereditary Sensory Neuropathy Type 1 | Sclerosing Cholangitis | Carbohydrate Metabolism Disorders | Spondylosis | Nestor-Guillermo Progeria Syndrome | Fibrillation, Atrial | Congenital Poikiloderma | Dermatitis | Leber Hereditary Optic Neuropathy | Melanocytic Nevus | Epidermolytic Palmoplantar Keratoderma | Aceruloplasminemia | Myeloid Leukemia | Prune Belly Syndrome | Blue Nevus | Fanconi Syndrome | Androgenic Alopecia | Glaucomatocyclitic Crisis | Congenital Bile Acid Synthesis Defect | Reye Syndrome | Spinal Muscular Atrophy | Porphyria, Acute Intermittent | Tibial Muscular Dystrophy | Multifocal Motor Neuropathy | Lipid Storage Diseases | Hypervalinemia | Asthma, Exercise-induced | Autoimmune Disease | Woodhouse-Sakati Syndrome | Bloom Syndrome | Eiken Syndrome | Tuberculosis | VEXAS Syndrome | Haim-Munk Syndrome | Polymyositis | Communication Disorders | Thrombocytopenia | Pituitary Dwarfism | Congenital Stationary Night Blindness | Takenouchi-Kosaki Syndrome | Ventricular Septal Defect | Myotonia | Cataplexy | Wolfram Syndrome 2 | Hyperuricemic Nephropathy, Familial Juvenile | Eccrine Porocarcinoma | Neutropenia | Non-Langerhans Cell Histiocytosis | Leukoplakia | Priapism | Esophageal Carcinoma | Fetal And Neonatal Alloimmune Thrombocytopenia | Wiskott-Aldrich Syndrome | Congenital Fiber-type Disproportion Myopathy | Shprintzen-Goldberg Syndrome | GNE Myopathy | Pure Autonomic Failure | Atelosteogenesis Type 1 | Traboulsi Syndrome | Lattice Corneal Dystrophy Type 1 | Familial Advanced Sleep Phase Syndrome | Hypohidrotic Ectodermal Dysplasia | Hypothalamic Obesity | Rhabdoid Tumor | Lymphangioleiomyomatosis | Chronic Lymphocytic Leukemia | Congenital Hypofibrinogenemia | Maple Syrup Urine Disease | Ophthalmia, Sympathetic | Waardenburg Syndrome Type 2A | Zellweger Syndrome | Cousin Syndrome | Tuberculous Meningitis | Epicondylitis | Cysticercosis | Keratitis | Multiple Sulfatase Deficiency | Angiosarcoma Of The Breast | Heart Block | Jalili Syndrome | Salla Disease | Gestational Trophoblastic Disease | Sponastrime Dysplasia | Spinal Muscular Atrophy Type 3 | Amyotrophic Lateral Sclerosis, Juvenile | Ganglioneuroma | Sialoadenitis | Melanoma | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Demyelinating Diseases | Oligospermia | Reticular Dysgenesis | Borjeson-Forssman-Lehmann Syndrome | Compartment Syndrome | Nevus | Acute Anterior Uveitis | Ichthyosis | Desmosterolosis | Carcinoma, Small Cell | Alagille Syndrome | Osteomalacia | Myopia | Stuve-Wiedemann Syndrome | Lactose Intolerance | Familial Male-limited Precocious Puberty | Nephroblastoma | Cardiomyopathy, Dilated, 1L | Pemphigus Foliaceus | Lymphoma | Anuria | Lamellar Ichthyosis | Evans Syndrome | Progressive Familial Intrahepatic Cholestasis | Juvenile Myelomonocytic Leukemia | Autonomic Neuropathy | Ataxia-ocular Apraxia 2 | Urethritis | Bursitis | Hemosiderosis | Microcephaly, Seizures, And Developmental Delay | Anorectal Malformations | Osteogenesis Imperfecta Type II | Partington Syndrome | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Nephrocalcinosis | Liddle Syndrome | Glycogen Storage Disease Type 4 | Pontocerebellar Hypoplasia Type 7 | Contact Dermatitis | Duchenne Muscular Dystrophy | Lipodystrophy | Zygomycosis | Seborrheic Dermatitis | Combined Deficiency Of Factor V And Factor VIII | Charcot-Marie-Tooth Disease, Type 1A | Hyperandrogenemia | Glycogen Storage Disease Type 1b | Blepharitis | Amyloidosis | Lymphopenia | Renal Failure | Creutzfeldt-Jakob Disease | Early Infantile Epileptic Encephalopathy 1 | Cholestasis, Intrahepatic | Polycystic Ovary Syndrome | Antisocial Personality Disorder | Jacobsen Syndrome | Hidradenitis | Ependymoma | Hypereosinophilic Syndrome | Transthyretin-related Amyloidosis | Giant Cell Glioblastoma | Familial Glucocorticoid Deficiency | Nutrition Disorders | Superficial Spreading Melanoma | Lewy Body Dementia | Familial Partial Lipodystrophy | Feingold Syndrome | Ocular Albinism Type 1 | Keratosis, Actinic | Protein C Deficiency | Arrhythmogenic Right Ventricular Cardiomyopathy | Hyperparathyroidism, Primary | Asperger Syndrome | Dystonia | Polymicrogyria | H Syndrome | Congenital Tufting Enteropathy | Hypoproteinemia, Hypercatabolic | Bethlem Myopathy | Pycnodysostosis | Perivascular Epithelioid Cell Tumor | Early Infantile Epileptic Encephalopathy 13 | Cancer, Skin | Retinal Coloboma | Bacterial Meningitis | Anencephaly | Cabezas Syndrome | Basan Syndrome | Alopecia Areata | Astrocytoma | Obesity, Morbid | Charcot-Marie-Tooth Disease Type 2E | Hyperparathyroidism-jaw Tumor Syndrome | Inflammatory Linear Verrucous Epidermal Nevus | Kohlschutter-Tonz Syndrome | Japanese Encephalitis | 3C Syndrome | Pulverulent Zonular Cataract | Osteogenesis Imperfecta Type IV | Pitt-Hopkins Syndrome | Cramp Fasciculation Syndrome | Antisynthetase Syndrome | Chiari Malformation Type I | Hepatoblastoma | Brachial Plexus Neuropathy | X-linked Creatine Transporter Deficiency | Progressive Familial Intrahepatic Cholestasis Type 1 | Tic Disorder | Craniofrontonasal Syndrome | Argininosuccinic Aciduria | Plasma Cell Leukemia | Neutrophilia | Benign Familial Infantile Seizures | Ovarian Hyperstimulation Syndrome | Dermatofibrosarcoma | Ectrodactyly | Primary Biliary Cholangitis | Greig Cephalopolysyndactyly Syndrome | B-cell Prolymphocytic Leukemia | Meleda Disease | Dental Caries | Rift Valley Fever | Birk-Barel Syndrome | Focal Dermal Hypoplasia | Neurotoxicity | Headache | Zollinger-Ellison Syndrome | Open-angle Glaucoma | Language Disorders | Prostatitis | Charcot-Marie-Tooth Disease Type 3 | Generalized Epilepsy With Febrile Seizures Plus | Epilepsy | Neurodevelopmental Disorders | Subcortical Band Heterotopia | Temtamy Preaxial Brachydactyly Syndrome | Proctitis | Tinea | Hypertension, Renal | Sotos Syndrome | Pouchitis | Erdheim-Chester Disease | Autosomal Recessive Spastic Paraplegia Type 75 | Congenital Afibrinogenemia | Sweet Syndrome | Christianson Syndrome | Hereditary Mixed Polyposis Syndrome | Myocarditis | Usher Syndrome Type IIC | Autonomic Nervous System Disorders | Familial Exudative Vitreoretinopathy | Mannosidase Deficiency Diseases | Episodic Ataxia | Guillain-Barre Syndrome | Optic Neuropathy, Anterior Ischemic | Disseminated Intravascular Coagulation | Neovascular Glaucoma | Sensory Neuropathy