Glioma

About the Disease
Glial Tumor, also known as glioma, is related to optic nerve glioma and brain stem glioma. The drugs Trametinib and Dabrafenib have been mentioned in the context of this disorder. Affiliated tissues include brain, t cells and bone marrow.

Common Targets
CD1C | HLA-DQB1-AS1 | HNMT | SHTN1 | TCF7L2 | MMP1 | NACAD | PLCG2 | DCAF4L2 | XRCC1 | YES1 | NRXN3 | PCGF2 | OR4P4 | UTS2B | SELE | ISL1 | G6714 | TBXAS1 | OR4C15 | CFAP44 | HLA-DQB1 | RASSF1 | TEKT5 | KCNJ11 | ABCA13 | LLGL1 | Mitogen-activated protein kinase p38 (MAPK p38) (nonspecified subtype) | MIR221 | PPP2R5A | HCK | PVT1 | COL3A1 | CFAP57 | CTNNB1 | DNA Methyltransferase (DNMT) (nonspecified subtype) | OR5M8 | CLIP4 | C2orf88 | MYNN | GUF1 | ITGAM | Glutamate Receptor Ionotropic AMPA Receptor | ERICH5 | FUT5 | CAT | AFF4 | FUBP1 | TRIM3 | SIX2 | RHOJ | HTR7 | AURKA | NTRK2 | SH3TC2 | FMO4 | POLD1 | SLC22A14 | DLEC1 | DNA-Directed DNA Polymerase Complex | CRYBG1 | G472 | NFKB1 | ZNF37A | BIVM-ERCC5 | HEATR3 | MIR149 | MATN3 | ERCC5 | ABL1 | BCL2L12 | ENPP2 | GJB2 | SSX7 | RPA4 | H3-3A | TRIM16L | Vascular endothelial growth factors (VEGF) (nonspecified subtype) | G1956 | FGR | MED13L | UGT1A10 | DYM | BICRA | Cyclin B (nonspecified subtype) | ITPR2 | AMOT | SMARCC1 | MST1R | NBN | PRDX1 | PIK3R5 | KLK9 | G3576 | RRAGC | G3845 | SPP1 | OLFML2A | MLH1 | GLRA1 | RECQL4 | LMF1 | EDNRA | UTY | STN1 | ECRG4 | SLK | B4GALNT2 | Protein farnesyltransferase | PRR36 | PRDM9 | IL6ST | MDM4 | MIP | MYO15A | DSE | RORC | CCDC26 | KIF13A | MAMDC4 | ZBTB16 | ALPL | PLPP7 | ISY1-RAB43 | IL1B | PIEZO2 | LDLR | DPYD | MLKL | CALHM5 | SPINT2 | TENM2 | TNKS1BP1 | TAPT1 | PFAS | TNFRSF25 | TIMM21 | SLC26A9 | MUC17 | GSR | H3-3B | HCN3 | TARS3 | ITGA1 | RFX7 | TAFA5 | MAP1B | EPHB2 | PDGFB | LPAR2 | UNC45A | SH3BP5 | CFB | FOLR2 | Chromosome 17 open reading frame 47 | N4BP1 | KIF2B | OR9G4 | IL12B | CRABP1 | TNFSF14 | CLCNKB | Integrin alphaMbeta2 (MAC-1) Receptor | ITIH2 | Carbonic Anhydrase (nonspecified subtype) | ETV4 | MYO7B | ACOT11 | OR11A1 | MAGEC3 | CCBE1 | SERPINA6 | KLK8 | TBC1D26 | G3569 | HORMAD2 | G6774 | CRTC2 | MYH9 | NOTCH3 | AKAP9 | CDK2 | GCC2 | Kainate Receptor (GluR) (nonspecified subtype) | G7015 | GRB10 | ACVR1C | MIR134 | TLR3 | GPATCH2 | PRKACG | IKZF5 | LCE3D | RALGPS1 | MCOLN2 | EVA1A | TRIM15 | ATG7 | CSK | Metabotropic glutamate (mGluR) receptor (nonspecified subtype) | ST14 | TFRC | THBS1 | IL36A | KIAA1217 | DIS3L2 | DAB1 | EPCAM | SBNO2 | OPHN1 | G2335 | TNRC6A | CANX | LATS1 | GRM5 | PKHD1L1 | SLIT2 | RAI1 | TMBIM6 | SPEM2 | NLRP11 | MSH3 | GSTA5 | FEN1 | MOCOS | TGOLN2 | BTK | ERCC1 | VAV1 | YTHDF2 | HDAC6 | MARK4 | COL8A2 | DOCK11 | ARCN1 | EXT2 | OPN5 | VEGFB | NT5DC3 | SLC25A4 | PCDHA3 | RIPOR2 | CENPX | ZNF652 | CRIM1 | HDAC2 | GREB1 | IL13RA2 | LIPI | ADGRF4 | CIC | LTV1 | HDAC8 | ABCC12 | NR1I3 | TTC7B | SMO | ZNF100 | GLIS3 | TRIM5 | CCNH | RAB11B | TRAF3 | ATP1A1 | NFATC1 | ABCB5 | G3620 | EXTL1 | MYO9B | FGFR2 | TOR4A | HCP5 | JCAD | TMEM132B | TMPRSS7 | Integrin alphavbeta3 (vitronectin) receptor | MIR1915HG | DDIAS | NOS1 | SYNE2 | NUP214 | USP26 | DNAJC25 | PDZD8 | SFRP2 | CDKL5 | DHRS7 | ALG2 | LAMB1 | EPHB3 | PRPSAP1 | SUPT7L | FLNC | FAT4 | FAM13A | SLC25A47 | PRMT5 | IFI44L | MBOAT2 | KPRP | CCDC169-SOHLH2 | PCDHA2 | DYNC1H1 | NR3C2 | DNAH3 | NPSR1 | TPMT | SLC16A8 | GALNT8 | MORC1 | G59272 | G595 | SCNN1A | NUP210 | SIPA1L1 | HIF1A | KMT2C | BMI1 | CPLANE1 | METTL24 | RASGEF1A | COBLL1 | PMS1 | NPC1L1 | CEP250 | PTPRZ1 | DDIT4L | JARID2 | Thioredoxin-disulfide reductase (TrxR) (nonspecified subtype) | FAT1 | ZAN | CDK18 | GALE | GPNMB | TXNRD2 | RAD52 | MTX3 | NLRP5 | RPS6KA3 | MSH4 | FBXO46 | SPHKAP | PLEKHO1 | ARIH1 | SEMA3E | RASGRF1 | SCN3A | FLG | BCAN | NPM1 | NRAS | DSTYK | CDK6 | MUC16 | TMPRSS4 | HRAS | STAT6 | OR4M1 | AKAP6 | MIR155 | HERC5 | SLC7A5 | TRIM58 | SRPK3 | PALD1 | ATRX | DHRS9 | CDA | RDX | JAG2 | KCNA4 | SPAM1 | WNT9B | NEDD4L | PRKCA | ATP13A5 | TGFB1 | XRCC2 | Protein Kinase B (PKB/Akt) (nonspecified subtype) | CNR2 | Folate Receptor (nonspecified subtype) | NF-kappaB (NFkB) | ZFAS1 | NDUFB9 | DLGAP4 | SOSTDC1 | OSTF1 | NMRK1 | AXL | CHRNE | Phosphatidylinositol 3-kinase (PI3K) (nonspecified subtype) | MIR138-1 | FAN1 | XAF1 | ABCB8 | Hedgehog Protein (nonspecified subtype) | Ephrin Receptor (nonspecified subtype) | G207 | FKBP1A | ALOX12 | GPT2 | T-Type Calcium Channel | Ribonucleoside-diphosphate reductase | PCNX3 | HAUS5 | PEX11B | IRAK3 | TNC | NHS | LARP4B | GPN3 | PHF21A | MICALL1 | MTBP | WASHC1 | OCLN | CFHR1 | KLHDC7A | LCK | PLCL2 | EHMT1 | IFIT5 | MYSM1 | Protein kinase C (nonspecified subtype) | MIR17HG | G7099 | MMP3 | CA12 | GABRB2 | DENND2A | LAG3 | CD3 Complex (T Cell Receptor Complex) | G5133 | CARD11 | LNX1 | SP140 | RGSL1 | TEX15 | OLFML3 | HLA-DQA1 | HNRNPH2 | CSF1R | CHD5 | RAX2 | LOC102724428 | BRD2 | PLS3 | POLE | PPARA | KLK11 | LIN28B | KIT | LINC02231 | G1950 | TRPM1 | MSH5 | ARHGAP24 | G842 | EML4 | FRY | PRX | CILP2 | SDR16C5 | ACSL3 | PRR14L | OR4N4 | CDKAL1 | SKIC8 | XRCC6 | PTRH2 | CCDC88B | CDK4 | ZDHHC21 | G7295 | PHB1 | mTOR complex 1 | RAD54B | GLI3 | TNFRSF18 | CDKN2B | G29126 | ING1 | DHODH | CYTB | KAZALD1 | USP53 | OR10AG1 | ANXA5 | G5728 | KRT5 | LCA5 | FAM9B | MAOA | P2RX3 | PEG3 | IL4R | TOP1 | SLC22A24 | GSDMA | IDH1 | AK7 | G4780 | ADGRE3 | HSF1 | CDK9/Cyclin T1 | UGDH | G7852 | PMS2 | FPGT-TNNI3K | SMG9 | HLA-B | SPTA1 | GRM2 | ANO8 | PRDM14 | LDLRAD1 | ARID2 | CDK2AP1 | TREH | TAF1D | MCF2L | TMTC1 | ERRFI1 | DZANK1 | IGFN1 | RALGAPB | DMRT3 | LRIG3 | G4851 | DDR2 | CLASP1 | PIK3CB | TAX1BP3 | FAT3 | BRCA2 | STC1 | ERBB3 | SNX7 | DDX19A | TEX11 | DCAF1 | BCR | SH3TC1 | GPR4 | MAP2K1 | EDDM3A | FRMPD4 | SERPINA7 | TRPM8 | PIK3R1 | CPSF1 | CYP4F12 | DACH1 | NOD2 | DNAH5 | FAT2 | UGT2B4 | MZF1 | PSD3 | BRD4 | HLA-DRB1 | SLC6A17 | NOTCH4 | CIT | LINC01122 | ELP1 | POU5F1 | SLC35E3 | HTATIP2 | HDGF | HEPH | CDKL3 | PIK3CD | SULT1B1 | UBE2S | TOPORS | HARS1 | COL5A1 | TEKT4 | DNA Topoisomerase II (nonspecified subtype) | PHLDB1 | TBC1D12 | MOB3B | ADAM22 | SEMA4F | PRPF8 | DRD2 | HULC | FGFR3 | ZFHX4 | DPPA4 | NAV2 | ARAP2 | OR6S1 | Chloride channel (nonspecified subtype) | ARHGAP36 | LINC02908 | FZD7 | ZBTB37 | ZC4H2 | ARL14 | NKD1 | SCAMP2 | CDK9 | SCNN1G | WNK3 | CFHR5 | FOXP1 | CHAF1A | CLEC2D | DOCK4 | TLX1 | PNMA5 | CNR1 | Raf kinase (nonspecified subtype) | HMX2 | SFRP4 | SHC1 | G673 | DKK1 | TAF3 | MPHOSPH6 | ADGRE1 | ZFHX3 | KAT6A | CFAP43 | PFKFB4 | HDAC3 | AVIL | AOC2 | MPP4 | MAP7D3 | PNPLA8 | XKR6 | SFXN5 | ROS1 | IL-4 receptor | LARS1 | PDK4 | NKD2 | FSTL5 | CD44 | SLCO1B7 | KRT8 | DLG3 | CDKN2B-AS1 | TMEM178A | SCP2 | Integrin alpha5beta1 (VLA-5) receptor | PMEL | GALNTL5 | SLC44A4 | ADAM18 | CD40 | DNAH6 | XPO1 | CEP290 | BRD1 | FACT complex | Estrogen receptor (nonspecified subtype) | MKI67 | TRPV2 | UTS2R | G5595 | CETN1 | POLQ | Neurotrophic Tyrosine Kinase Receptor (TRK) (nonspecified subtype) | TGM2 | MYT1 | SSX3 | G1029 | ADAMTSL1 | HAS3 | CD8 | DTX3L | LHB | C3AR1 | SH3BP4 | MGAT4C | GPX1 | PDGFRB | Integrin alphavbeta5 receptor | KIF5B | GIMAP8 | RBM12B | SOD2 | SPRR4 | MIR335 | OR51B2 | PHF2 | USP32 | RPS6KC1 | PTCH2 | G142 | SPTY2D1 | NSD1 | OR6C70 | ACO2 | DOCK5 | MTDH | GNB5 | KLRK1 | NTRK3 | FLOT2 | ENTPD3 | OR2Y1 | WNK2 | RNF148 | WASHC2A | MIR424 | TMEM25 | ZCCHC8 | AHSA1 | TPTE | ZNF707 | GRIA4 | MIB1 | HSPG2 | CPEB3 | MGA | TTI2 | P3H2 | PCDHGA7 | HDAC1 | YLPM1 | MPG | LRRC31 | LINC00673 | CCNT1 | DNAH8 | TET2 | CEP192 | LONP1 | LILRB3 | SHISA9 | FCGR3A | RAB11FIP1 | PSD4 | KCNMB3 | ADORA2A | SMS | TNKS2 | PIWIL4 | PIKFYVE | MUC5B | ADNP2 | ZGPAT | CPEB2 | TOPAZ1 | TDG | MUC1 | G4609 | TRPV1 | AHNAK | LILRB2 | ZDHHC8 | MAPK8IP3 | OLIG2 | PCDHGA6 | PTCH1 | STAT5 (nonspecified subtype) | LOC339166 | LAMC2 | DLG4 | ASCL1 | EFEMP1 | CCDC180 | NFE2L3 | MAP4K1 | ELAPOR1 | TGFBR1 | PI4KA | MTMR3 | PTGS1 | SOX5 | STIM1 | ALOX15B | COL1A2 | CSMD1 | CDKN2A-DT | KCNH6 | POT1 | STK32C | STYK1 | EBP | INHBA | MX1 | RTKN2 | SKAP1 | MLH3 | ABCC9 | CEBPB | DNHD1 | PP2D1 | CASP8 | PIK3C2G | SOCS3 | GTF3C3 | HLA-A | SLC22A2 | ARSF | ASS1 | SRPX | OR2M4 | IARS2 | PAPOLA | C17orf67 | ERCC3 | MAGI3 | RC3H2 | CCDC141 | TMEM174 | NTRK1 | BLTP1 | LOC100287944 | PCLO | GSK3B | MFN2 | OR14C36 | MIR210 | SERPINE1 | RCOR3 | PDE4DIP | DCDC2B | SHOC1 | TSPO | SPATA5L1 | DGKZ | NRP1 | PRPF4B | TRIM59 | G9429 | WRNIP1 | HOXA2 | DNAH2 | DNAH12 | CLDN5 | FGB | SUV39H2 | CDKN2C | DCX (DDB1-CUL4-X-box) E3 protein ligase complex | RYR2 | EVC2 | INSRR | SPANXC | MEN1 | RMI1 | G2475 | PROZ | ACVR1 | LGALS13 | PHACTR3 | Interferon alpha/beta Receptor (nonspecified subtype) | CPEB4 | CDH19 | CD70 | BICD1 | SMARCA4 | LHX9 | Interferon (nonspecified subtype) | OR52B6 | COL4A2 | RASSF6 | SEZ6L2 | KRT6C | LILRA2 | ADCY8 | CDK1/Cyclin B | XRCC3 | UGT1A5 | SPRY2 | CD163 | FKBP9 | SELPLG | RBM46 | MBL2 | TLR2 | MME | SLC37A2 | NCL | ATP7B | MIR429 | CXCL12 | Triacylglycerol Lipase (TG Lipase) (nonspecified subtype) | VIPR2 | RTEL1 | TES | LBX1 | ACKR3 | QSOX1 | R3HDML | DAPK1 | LIPC | PAM | ZFPM2 | ACSL5 | MAML2 | FLT4 | PAM16 | HMCN1 | SACS | GUCY1A1 | KRTAP21-1 | G3480 | AFAP1 | AGR3 | SOD3 | MYH14 | PRKDC | NRXN1 | TAS2R60 | EPHB6 | DCAF7 | STK3 | CNTN3 | ZNF718 | CBS | mTOR complex 2 | PJA1 | Glycogen synthase kinase 3 (GSK-3) (nonspecified subtype) | LRP1 | BPTF | CD93 | PDE4C | POLR3B | CD33 | GALNT11 | beta-Adrenoceptor (nonspecified subtype) | SOAT1 | TONSL | ERMP1 | FOLH1 | CBL | CCDC170 | MBD3L1 | TNFRSF11A | PPP2R2C | PPP5C | DNAH7 | Elastase (nonspecified subtype) | LRRC4 | PRUNE2 | ADGRF3 | ZNF215 | ZNF609 | ATP2C1 | OTUD7B | CKAP5 | STARD4 | ZNF672 | IL26 | ERCC2 | MYH4 | TCIRG1 | PTPN3 | IDH2 | SPIN2B | KAT2A | POU4F2 | PTCHD3 | TRPM2 | LIN28A | ZNF665 | ATP8B4 | SDK2 | RANBP2 | FAAH | ESPN | PPFIA2 | MYO1B | MAPK15 | DET1 | RAVER2 | Platelet-Derived Growth Factor Receptor (nonspecified subtype) | KLHL25 | Mitogen-Activated Protein Kinase (nonspecified subtype) | ADAMTS16 | FLT1 | FRK | ZNF44 | GHR | ACVR1B | FGF19 | SC5D | CSF2 | MCF2L2 | G836 | LINC02740 | CREBZF | RAD51 | OR56B1 | THBS4 | FMOD | UNC5C | HBD | NFKBIZ | MCM3 | G7157 | DLL1 | CD3E | CDC25A | CPE | LAMA2 | LDHA | C6 | TYRO3 | ABTB1 | POU3F3 | ANKHD1 | DIPK1C | FAM168B | COL19A1 | CDK2/Cyclin A | SOX9 | SLC16A11 | GSDME | ASB18 | TBX6 | F5 | PREX2 | SERPINF2 | GRM3 | EP400 | BLK | SI | SST | G4318 | MSN | FGFR1 | ROR1 | ARHGEF5 | PDE2A | KLRC4-KLRK1 | GPM6A | ZDBF2 | CD84 | HID1 | PCDHGA1 | ZBTB46 | SFRP5 | RASSF10 | CLEC4M | TNFRSF17 | UNC45B | TLL1 | KAT6B | SLC14A2 | SLC4A4 | PROM1 | LRRC1 | GJB6 | RNASE4 | LRGUK | ZNF568 | NPSR1-AS1 | SLC26A2 | TGFB2 | NBAS | NLRP2 | PCDHB15 | RAF1 | OR4D2 | UBLCP1 | ENPEP | UBTD1 | MCHR2 | ARFGEF1 | PROKR1 | RYR3 | ASB10 | RDH10 | SLC22A10 | ZNF800 | FASN | SIK2 | COL6A2 | STK4 | OR4C12 | PROS1 | FAF1 | KCNT1 | GLIPR1L2 | PARP12 | KCNQ1 | MIR125A | USH2A | DDR1 | PAPPA | POLR2A | GRHPR | KRTAP10-8 | LINC02389 | EPHA2 | FGFR4 | ZNF500 | GRK5 | APEX1 | PTN | MUC21 | CLPP | GJA1 | KLRG2 | TRIM49C | REEP1 | Janus Kinase (nonspecified subtype) | ZNF226 | PIM1 | PHF19 | C11orf24 | BSN | PVR | RB1 | Poly [ADP-ribose] polymerase (nonspecified subtype) | ERN1 | NEFH | USP11 | BMP10 | PRKCB | G4193 | ZNF469 | POLR2B | CCNB1 | IL16 | LTBP4 | INTS8 | SETD1A | RBL2 | MCM5 | BRD3 | ZNF430 | TMEM87B | GPX4 | XRCC4 | PPP1CC | SYNRG | MSI2 | CYP2C9 | DSC3 | NOS3 | PPP1R12C | MYB | CLUH | FUT10 | PON1 | PTCHD1 | KCNS3 | OR1S1 | ZNFX1 | AHNAK2 | SYT10 | RFX4 | CPNE8 | Tubulin | VCX | TNFRSF10D | LGR4 | IGF2BP3 | PSG3 | FASLG | CXCR2 | TNXB | OR10Q1 | G2069 | MSR1 | MAU2 | KCNG4 | OTOF | CTCF | TMEM179B | DMBT1 | LYN | VRK2 | UNC80 | SUB1 | ACYP2 | OVOL2 | EIPR1 | MYO1D | ATOH8 | HCCS | CLEC2B | CRAMP1 | PODN | ERCC4 | MUC4 | PIP | HAVCR2 | CFAP46 | BAZ1B | TTN | PPP1R14C | PHF7 | CDAN1 | TIGIT | PBRM1 | MAGI1 | FNDC3A | EPB41L3 | ARHGAP45 | OSMR | MAP2K2 | DENND3 | CACNA1E | ANKFY1 | SERPINA11 | ORMDL3 | GJB4 | SIK1 | TACR1 | ZNF616 | ACSM6 | ENGASE | MMP2 | PIWIL3 | FBXL18 | RAVER1 | LIPE | ERBB4 | SMC5 | SRA1 | GUCY2C | HLA-DPB1 | FANCA | SDK1 | TLR9 | RAG1 | LRP2 | SYNE1 | CHD6 | MARCHF1 | TIMM44 | JADE3 | Cyclin A (nonspecified subtype) | CTLA4 | FER1L6 | R3HDM2 | G5743 | ANTXR2 | SUV39H1 | UTRN | NF1 | NAMPT | G3082 | VARS2 | ANKEF1 | DNAJC7 | ZNF177 | ATP6V1A | LMBRD2 | G4233 | C3 | WT1 | COMMD4 | ARHGAP18 | TNFRSF8 | HNF4A | ALPK2 | MIR146A | SGMS1 | PIK3CA | ANGEL2 | CD3D | RRAS | ITGAL | XRCC5 | TANGO6 | TUBGCP4 | PARP2 | CD47 | HPSE2 | NOS2 | LRP1B | ABCB11 | RNF113A | SCRN1 | RIPK3 | ZNF618 | G7124 | GGTLC1 | ROBO1 | ATG3 | SH3BP2 | SMARCB1 | GTPBP10 | KIF16B | STARD9 | APOB | C10orf71 | SFRP1 | BEST3 | ETFA | ARHGAP33 | LPA | TRPC1 | MUS81 | CD28 | SPATA2L | SLIT1 | OR52E8 | SLC5A8 | G2064 | GMEB2 | CADPS2 | IL36G | LRRFIP2 | CDC42 | EGFLAM | MRPS26 | UMPS | FLT3 | POLR2E | EBAG9 | EXOC3L4 | G925 | DRC1 | KMT2D | PAK4 | ZNF446 | IGF2BP2 | TSBP1 | CSF2RB | ARHGAP4 | CLDN18 | FYN | GNAS | BTBD7 | POLR3A | COL2A1 | ARHGEF28 | PLEKHM3 | NQO1 | EPS8 | MYCN | AKT3 | GAS2L3 | TRPA1 | AIP | SLC30A8 | ATF5 | FOXC1 | GRPR | SLC2A4RG | BIRC5 | AQP1 | PLPP4 | FTO | NEK11 | TRAPPC12 | PCP4 | FCHSD1 | CDC42EP3 | DCLRE1A | PTPN11 | COL6A3 | SLC31A1 | MTHFD2L | PDGFRA | MMP20 | CCDC168 | C2orf80 | OR4C6 | FCER1A | MLC1 | TMEM52 | NEGR1 | KIF1A | HNF4G | KLF12 | UGT3A1 | IL10 | CCL2 | Dual Specificity Mitogen-Activated Protein Kinase Kinase (MEK) (nonspecified subtype) | ADSL | OR4X1 | DOP1A | GRN | DOP1B | ICAM3 | PGK1 | DNAH14 | CP | CYP27B1 | TGFB3 | ZNF18 | NAA11 | LARP6 | PCDHAC1 | Proteasome Complex | RET | SIX1 | CX3CR1 | DAXX | MUC20 | TXNDC11 | H3C2 | THOC5 | PELO | DKK3 | FAM114A2 | NLRP3 Inflammasome | OR5D14 | MYH8 | MLLT10 | NCOA1 | CFLAR | TOP2A | NEK1 | GNA11 | IL22RA1 | MIR196A2 | MGMT | ARID1A | G5243 | DLGAP2 | TAOK2 | CEACAM19 | CEACAM3 | FTSJ3 | VTI1A | RHBDF1 | Histone deacetylase (nonspecified subtype) | GOLGA3 | WDHD1 | CHST14 | DRD3 | CACNA2D3 | RP1L1 | KLF8 | IL4 | SLC13A3 | SLC6A6 | ADAM33 | ALOX5 | CDK1 | Voltage-Gated Calcium Channel alpha-2/delta (nonspecified subtype) | ZKSCAN2 | MYO5B | ANKRD17 | PLAUR | SLCO1C1 | NDST3 | POP1 | TBC1D20 | OR5T3 | GLP1R | RTEL1-TNFRSF6B | CTIF | VCAN | TMEM64 | NOA1 | RSL1D1 | RNASEL | MATN1 | STK38L | RRM2B | CD276 | R3HDM4 | HELB | ISG20 | TRPC3 | KDM7A | RAB27A | SLC30A4 | PI3 | ARFRP1 | C6orf15 | LIPG | HK3 | AHRR | CMA1 | SIX3 | F8 | MIR499A | NEK5 | CYP19A1 | MAP3K3 | OR5AS1 | ARMT1 | PDE3A | HECTD4 | COL7A1 | DNAH9 | CEP78 | HOTAIR | RASSF2 | JAK3 | BNIPL | STYX | ELF5 | SSUH2 | G238 | RAB27B | UPF1 | IL13 | NOTUM | TP53BP2 | TRPM3 | RASSF5 | MFSD9 | FANCM | UBE2O | TEX55 | G7422 | LRIG1 | AGBL4 | JAK1 | DQX1 | NGF | LINC01565 | SPEF1 | RAD54L | POU2AF1 | GNAZ | SPECC1 | PCDHA11 | SLC27A3 | DIAPH1 | HLA-C | ZMIZ1 | PRAMEF4 | HAAO | GRIN2B | MBD5 | RAPGEF5 | Fibroblast Growth Factor Receptor (FGFR) (nonspecified subtype) | RAET1G | G5347 | ESRP1 | GPR55 | CHEK2 | TNFRSF9 | TBC1D15 | TGFBI | HHIPL2 | POMK | TSPEAR | MSH6 | RABIF | NOM1 | MSH2 | CRBN | ALOX15 | UPF2 | GLYATL1 | MED12 | LIG4 | INPP5F | TLR7 | PTGFRN | G114548 | KDR | AGTPBP1 | PIK3CG | LATS2

Note: If you'd like to get a target analysis report for Glioma, or if you are interested to learn how our AI-powered BDE-Chem can design therapeutic molecules to interact with the target(s) above against the disease of Glioma at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

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Rolandic Epilepsy | Leukodystrophies | Senior-Loken Syndrome | Von Willebrand Disease | Rheumatic Heart Disease | Heart Septal Defects | Cornelia De Lange Syndrome | X-linked Acrogigantism | Pyruvate Kinase Deficiency | Calcium Pyrophosphate Deposition Disease | Fukuyama Congenital Muscular Dystrophy | Hyperlipidemia | Saethre-Chotzen Syndrome | Paget's Disease Of The Breast | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Ovarian Hyperstimulation Syndrome | Myopathy | Arts Syndrome | Charcot-Marie-Tooth Disease Type 4 | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Pemphigoid | Leber Congenital Amaurosis | Hyperferritinemia-cataract Syndrome | Ectodermal Dysplasia | Spinocerebellar Ataxia Type 10 | Methemoglobinemia | Hairy Cell Leukemia | Lattice Corneal Dystrophy Type 1 | Oculocutaneous Albinism Type 1 | Sertoli Cell-only Syndrome | Microvillus Inclusion Disease | Chronic Enteropathy Associated With SLCO2A1 Gene | Intestinal Tuberculosis | Pseudohypoparathyroidism Type 1C | Kleine-Levin Syndrome | 3-M Syndrome | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Restless Legs Syndrome | Cramp Fasciculation Syndrome | Arteriosclerosis | Autoimmune Hemolytic Anemia | Megaloblastic Anemia | Nutrition Disorders | Spinocerebellar Ataxia Type 16 | Brachial Plexus Neuropathy | Episodic Ataxia Type 1 | Retinal Diseases | Granular Corneal Dystrophy | Coma | Spinocerebellar Ataxia Type 42 | Glycogen Storage Disease Type 3 | Amyloidosis | Glycogen Storage Disease Type 1b | Sporadic Hemiplegic Migraine | Fibrosis | Auriculocondylar Syndrome | Dysferlinopathy | Chronic Neutrophilic Leukemia | Infantile Spasm | Antithrombin III Deficiency | Tyrosinemia Type 1 | Sponastrime Dysplasia | Hyperandrogenemia | Angiomyolipoma | Amish Infantile Epilepsy Syndrome | Panuveitis | Endometrial Hyperplasia | Neuromyotonia | Cutaneous Lupus Erythematosus | Creutzfeldt-Jakob Disease | Pneumonia, Viral | Crigler-Najjar Syndrome | Dermatomyositis | Inflammatory Joint Disease | Muscle Wasting | Insulinoma | Bladder Exstrophy | Histiocytic Sarcoma | Combined Deficiency Of Factor V And Factor VIII | Charcot-Marie-Tooth Disease, Type 2A | Retinopathy Of Prematurity | Charcot-Marie-Tooth Disease, Type 2 | Takotsubo Cardiomyopathy | Nail Disorder, Nonsyndromic Congenital | Joubert Syndrome | Blood Protein Disorders | Sclerosteosis 2 | Cohen Syndrome | Cone Dystrophy | Enlarged Vestibular Aqueduct | Borjeson-Forssman-Lehmann Syndrome | Filariasis | Dental Caries | Hemorrhagic Disorders | Porphyria | Dengue Shock Syndrome | Necrotizing Autoimmune Myopathy | Spondylometaphyseal Dysplasia | Fahr Disease | Corneal Dystrophy And Perceptive Deafness | Usher Syndrome Type I | Preaxial Polydactyly | Cancer, Breast | Succinic Semialdehyde Dehydrogenase Deficiency | Guanidinoacetate Methyltransferase Deficiency | Hepatitis, Alcoholic | Hyperphenylalaninemia | Epithelioid Hemangioma | Xeroderma Pigmentosum | Papilloma | Leukocyte Adhesion Deficiency | Von Hippel-Lindau Disease | Poirier-Bienvenu Neurodevelopmental Syndrome | Early Infantile Epileptic Encephalopathy 13 | Persistent Fetal Circulation | Hepatitis B, Chronic | Primary Hyperoxaluria | Polycystic Kidney, Autosomal Dominant | Epidermolysis Bullosa Acquisita | Feingold Syndrome | Branchiootorenal Syndrome | Thrombasthenia | Proteus Syndrome | Congenital Hypofibrinogenemia | Alpha-thalassemia Myelodysplasia Syndrome | Fabry's Disease | Avellino Corneal Dystrophy | Nemaline Myopathy 10 | Thrombophilia | Endophthalmitis | Eating Disorder | Otitis Externa | Behcet's Disease | Carpal Tunnel Syndrome | DNA Ligase IV Deficiency | Arthritis, Reactive | Erythema Multiforme | Nephrotic Syndrome | Kernicterus | Infertility | Spinocerebellar Ataxia Type 14 | Parkinson's Disease | Molybdenum Cofactor Deficiency | Delirium | Parkinson Disease 6, Autosomal Recessive Early-onset | Osteoglophonic Dysplasia | Nicolaides-Baraitser Syndrome | Tyrosinemia | Vascular Calcification | Ellis-Van Creveld Syndrome | Pleomorphic Xanthoastrocytoma | Juvenile Myoclonic Epilepsy | Hyperinsulinism-hyperammonemia Syndrome | Metabolic Syndrome | Stiff-man Syndrome | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Hemolytic Uremic Syndrome | Psoriasis | Charcot-Marie-Tooth Disease, Type 2C | Neuroectodermal Tumors, Primitive | Endocarditis | Autosomal Recessive Bestrophinopathy | Rosacea | Glycogen Storage Disease Type 4 | Rhabdomyosarcoma, Embryonal | Craniolenticulosutural Dysplasia | Heart Block | CHARGE Syndrome | Familial Episodic Pain Syndrome | Bulimia Nervosa | Fetal Alcohol Syndrome | Rhinitis | Dengue Hemorrhagic Fever | Stromal Corneal Dystrophy | Astigmatism | Anorectal Fistula | Osteopathia Striata With Cranial Sclerosis | Vaginitis | Hydronephrosis | Werner's Syndrome | Autoimmune Disease | Neurofibroma | Impetigo | Beare-Stevenson Syndrome | Meesmann Corneal Dystrophy | Progressive Myoclonic Epilepsy | Orthostatic Intolerance | Large Granular Lymphocytic Leukemia | Peeling Skin Syndrome Type B | POEMS Syndrome | Lupus Erythematosus | Scoliosis | Porphyria, Acute Intermittent | Temtamy Preaxial Brachydactyly Syndrome | Pure Red Cell Aplasia | Cockayne Syndrome | Dyskeratosis Congenita | Spinal And Bulbar Muscular Atrophy | Miyoshi Myopathy | Hepatitis | Schwartz-Jampel-Aberfeld Syndrome | Chronic Idiopathic Myelofibrosis | Glioblastoma Multiforme | Salla Disease | Nager Acrofacial Dysostosis | Congenital Heart Block | Papillon-Lefevre Syndrome | Gastroenteritis, Eosinophilic | Rash | Spinal Muscular Atrophy | Narcolepsy | Schistosomiasis Mansoni | Alopecia Totalis | Eiken Syndrome | Granular Corneal Dystrophy Type 1 | Tylosis With Esophageal Cancer | Melanocytic Nevus | Heavy Chain Disease | Dysmorphophobia | Waardenburg Syndrome Type 4 | Periodic Limb Movement Disorder | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Oligodendroglioma | Tardive Dyskinesia | Haim-Munk Syndrome | Glycogen Storage Disease Type 6 | Polycythemia | HIBCH Deficiency | Nemaline Myopathy 8 | Teratozoospermia | 5-oxoprolinase Deficiency | Basal Cell Nevus Syndrome | McLeod Syndrome | Obesity | Portal Vein Thrombosis | Facioscapulohumeral Muscular Dystrophy Type 1 | Vitelliform Macular Dystrophy | Apraxia | Ichthyosis | Hereditary Hemorrhagic Telangiectasia | Keratocystic Odontogenic Tumor | Seizures-scoliosis-macrocephaly Syndrome | X-linked Charcot-Marie-Tooth Disease | Hyperinsulinemia | Adenomatoid Tumor | Norrie Disease | Optic Atrophy 2 | Bullous Pemphigoid | Polymyalgia Rheumatica | Maternally Inherited Diabetes And Deafness | Antley-Bixler Syndrome | Ghosal Syndrome | Familial Partial Lipodystrophy | Congenital Hereditary Endothelial Dystrophy Type I | Polydactyly | Epidermolysis Bullosa Simplex, Generalized | Pure Autonomic Failure | Shwachman-Bodian-Diamond Syndrome | Cancer, Colon | Neuromuscular Disorders | Erythematotelangiectatic Rosacea | Still Disease | Smoldering Myeloma | Seborrheic Dermatitis | Chromosome 9q34.3 Deletion Syndrome | Ataxia-ocular Apraxia 2 | Neurocysticercosis | C3 Glomerulonephritis | Fanconi Syndrome | Pain | Congenital Bilateral Absence Of Vas Deferens | Gardner Syndrome | Spinal Muscular Atrophy Type 3 | Dysgerminoma | Aldosterone Synthase Deficiency | Wolfram Syndrome | Polymicrogyria | Familial Dysautonomia | Speech Disorders | Cutis Laxa | Ganglioneuroma | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Congenital Myasthenic Syndrome | Vasculitis | Skin Fragility-woolly Hair Syndrome | Autosomal Recessive Spastic Paraplegia Type 75 | Swine Influenza | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Peroxisomal Disorder | Endometritis | Familial Pheochromocytoma-paraganglioma | Cardiac Sarcoidosis | Renal Hypouricemia | Parkinsonism | Agoraphobia | Evans Syndrome | Hepatoblastoma | Dystonia | Hyperostosis | Lymphoma | Tibial Muscular Dystrophy | Polycystic Liver | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Neurodegeneration With Brain Iron Accumulation | Antisocial Personality Disorder | Strabismus | Retinitis | Proteasome-associated Autoinflammatory Syndrome 2 | Choriocarcinoma | Myotonic Disorders | Retinitis Pigmentosa 3 | Gigantism | Atrial Septal Defect | Purpura | Robinow Syndrome | Hyper IgE Syndrome | Hidradenitis | Treacher Collins Syndrome | Spondyloperipheral Dysplasia | Cardiomyopathy, Peripartum | Asthma, Exercise-induced | Personality Disorders | Short-chain Acyl-CoA Dehydrogenase Deficiency | Congenital Aniridia | Bronchiolitis | Pitt-Hopkins Syndrome | Focal Cortical Dysplasia Type 2 | Niemann-Pick Disease | Spasticity | Autosomal Recessive Spastic Paraplegia Type 54 | Walker-Warburg Syndrome | Osteonecrosis | Contact Dermatitis | Chorea | Intestinal Hypomagnesemia 1 | Acrodermatitis | Urticaria | Common Cold | Diabetic Neuropathy | Presbyopia | Congenital Adrenal Hyperplasia 1 | Malonyl-CoA Decarboxylase Deficiency | Hypertriglyceridemia | Heterotopic Ossification | Anxiety Disorders | Epidermodysplasia Verruciformis | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Androgenic Alopecia | Osteopetrosis | Metachondromatosis | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Papillorenal Syndrome | Metaphyseal Chondrodysplasia, Schmid Type | Acute Anterior Uveitis | Multiple Sclerosis, Primary Progressive | Pelizaeus-Merzbacher Disease | Myofibrillar Myopathy | Frank-ter Haar Syndrome | Onchocerciasis | Pantothenate Kinase-associated Neurodegeneration | Angelman Syndrome | Colitis | Oculocutaneous Albinism Type 4 | Lichen Planus | Progressive Familial Intrahepatic Cholestasis | Jacobsen Syndrome | Obsessive-compulsive Disorder | Hemorrhage | Micropenis | Hyperinsulinemic Hypoglycemia | Thrombocytopenia | Aspergillosis | Otosclerosis | Glaucoma, Congenital | Chordoid Glioma | Knobloch Syndrome | Panniculitis | Myoclonus-dystonia Syndrome | Tricho-hepato-enteric Syndrome | Scabies | Choroiditis | Netherton Syndrome | Autonomic Neuropathy | Hypercalciuria | Hypercholesterolemia | Hypercholesterolemia, Familial | Thin Basement Membrane Disease | Zygomycosis | Phenylketonuria | Chronic Mucocutaneous Candidiasis | Erythromelalgia | Non-bullous Congenital Ichthyosiform Erythroderma | Waardenburg Syndrome | Rhabdomyosarcoma | Mucolipidosis | Otitis Media | Idiopathic Multicentric Castleman Disease | Lymphangioleiomyomatosis | Gallstones | Rubeosis Iridis