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Bioinformatics and Systems Medicine Laboratory Bioinformatics and Systems Medicine Laboratory

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TissGeneSummary

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TissGeneExp

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TissGene-miRNA

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TissGeneMut: TissGeneSNV, TissGeneCNV, and TissGeneFusions

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TissGeneNet

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TissGeneProg

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TissGeneClin: TissGeneDrug and TissGeneDisease

TissGeneSummary for GRIN2A
check button Gene summary
Basic gene informationGene symbolGRIN2A
Gene nameglutamate receptor, ionotropic, N-methyl D-aspartate 2A
SynonymsEPND|FESD|GluN2A|LKS|NMDAR2A|NR2A
CytomapUCSC genome browser: 16p13.2
Type of geneprotein-coding
RefGenesNM_000833.4,
NM_001134407.2,NM_001134408.2,
DescriptionN-methyl D-aspartate receptor subtype 2AN-methyl-D-aspartate receptor channel, subunit epsilon-1N-methyl-D-aspartate receptor subunit 2Aglutamate receptor ionotropic, NMDA 2A
Modification date20141222
dbXrefs MIM : 138253
HGNC : HGNC
Ensembl : ENSG00000183454
HPRD : 00698
Vega : OTTHUMG00000129721
ProteinUniProt:
go to UniProt's Cross Reference DB Table
ExpressionCleanEX: HS_GRIN2A
BioGPS: 2903
PathwayNCI Pathway Interaction Database: GRIN2A
KEGG: GRIN2A
REACTOME: GRIN2A
Pathway Commons: GRIN2A
ContextiHOP: GRIN2A
ligand binding site mutation search in PubMed: GRIN2A
UCL Cancer Institute: GRIN2A
Assigned class in TissGDB*C
Included tissue-specific gene expression resourcesHPA,TiGER
Specific-tissues in normal samples (assigned by TissGDB using HPA, TiGER, and GTEx)Brain
Cancer types related to the specific-tissues in cancer samples (assigned by TissGDB using TCGA)GBM,LGG
Reference showing the relevant tissue of GRIN2A
Description by TissGene annotationsCancer gene
Fused withTSGene
* Class A consists of genes with literature evidence and is part of the cTissGenes. Class B consists of only cTissGenes without additional evidence. The remaining genes belong to Class C.

check button Gene ontology having evidence of Inferred from Direct Assay (IDA) from Entrez
GO IDGO termPubMed ID
GO:0045471response to ethanol18445116
GO:0045471response to ethanol18445116


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TissGeneExp for GRIN2A

check button Gene expressions across 28 cancer types (X-axis: cancer type and Y-axis: log2(norm_counts+1))
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
gene exp


check button Gene isoform expressions across 28 cancer types (X-axis: cancer type and Y-axis: log2(norm_counts+1))
(TCGA pan-cancer tcga_rsem_isoform_tpm, version 2016-09-01)
gene isoform exp


check button Gene expressions across normal tissues of GTEx data
(GTEx GTEx_Analysis_v6_RNA-seq_RNA-SeQCv1.1.8_gene_rpkm.gct)
- Here, we shows the matched tissue types only among our 28 cancer types.
normal gene exp


check button Different expressions across 14 cancer types with more than 10 samples between matched tumors and normals (X-axis: cancer type and Y-axis: log2(norm_counts+1))
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
DEG exp

- Significantly differentially expressed cancer types and information. (|Fold change|>1 and FDR<0.05)
Cancer typeMean(exp) in tumorMean(exp) in matched normalLog2FCP-val.FDR
KIRP-0.6118476192.186996131-2.798843757.82E-096.09E-08
BRCA0.6837824252.119683302-1.4359008771.09E-124.87E-12
COAD-2.0661581960.931714881-2.9978730771.36E-134.45E-12
STAD1.2383805063.807883631-2.5695031258.09E-071.37E-05
KICH0.1777628811.523222881-1.345460.01980.033491328
LIHC-0.688159119-1.9684511191.2802920.00570.012931256
ESCA-0.009394213.668923972-3.6783181820.0007930.012508028
PRAD-0.1239639650.989697573-1.1136615383.16E-050.000151965
BLCA-1.9894745930.933656986-2.9231315795.76E-060.000125591


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TissGene-miRNA for GRIN2A

check button Significantly anti-correlated miRNAs of TissGene across 28 cancer types
(Gene-miRNA relations from TargetScanHuman Relsease 7.1, Conserved_Site_Context_Scores.txt.zip, 06.01.2016)
(TCGA IlluminaHiSeq_miRNASeq, log2(RPM+1) data, version 2016-11-21)
(TCGA IlluminaHiSeq_RNASeqV2, log2(normalized_count+1) data, version 2016-08-16)
(Spearman’s Rank Correlation (p-value<0.05 and coefficient<-0.25))
Cancer typemiRNA idmiRNA accessionP-val.Coeff.# samples
LUADhsa-miR-27b-3pMIMAT00004190.034-0.2860
UVMhsa-miR-30b-5pMIMAT00004200.012-0.2880
ACChsa-miR-373-3pMIMAT00007260.0099-0.2978
ACChsa-miR-373-3pMIMAT00007260.0099-0.2978


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TissGeneMut for GRIN2A
TissGeneSNV for GRIN2A

check button nsSNV counts per each loci.
Different colors of circles represent different cancer types. Circle size denotes number of samples.
(TCGA somatic mutation (SNPs and small INDELs) data, version 2016-04-25)

* Click on the image to enlarge it in a new window.
SNV lollipop
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check button Somatic nucleotide variants of TissGene across 28 cancer types
(X-axis: cancer type and Y-axis: % of mutated samples)
The numbers in parentheses are numbers of samples with mutation (nsSNVs).
(TCGA somatic mutation (SNPs and small INDELs) data, version 2016-04-25)
SNV distribution

- nsSNVs sorted by frequency.
AAchangeCancer type# samples
p.G1322ESKCM7
p.E962KSKCM3
p.R1067WSKCM3
p.D1153NSKCM3
p.G688ESKCM3
p.G20DSKCM2
p.E1175KSKCM2
p.R1022CLUAD2
p.R1067QSKCM2
p.D105NSKCM2
p.R1376CBLCA2
p.D1315NSKCM2
p.S1447FSKCM2
p.P699SSKCM2
p.E806KSKCM2
p.D1024NSKCM2
p.D344NSKCM2
p.E657KSKCM2
p.E1156KSKCM2
p.P1132LSKCM2
p.E743KSKCM2
p.P273SSKCM2
p.E1125KSKCM2
p.E1073KSKCM2
p.H1129YSKCM2
p.D731NSKCM1
p.R370QSKCM1
p.R1241QLUSC1
p.D78NUCS1
p.M817ISTAD1
p.E1175XCHOL1
p.G101RSKCM1
p.A968PLUAD1
p.N946SSKCM1
p.Q1278KKIRC1
p.A302TCOAD1
p.P401QLUAD1
p.G1127CBLCA1
p.R970WUCEC1
p.D234NSKCM1
p.H381YSKCM1
p.A643SHNSC1
p.D1195EHNSC1
p.V568FLUAD1
p.N490YLGG1
p.M133ISKCM1
p.G873EHNSC1
p.A638TCOAD1
p.A921TLGG1
p.S1403LSKCM1
p.V633ABLCA1
p.S1045FSKCM1
p.E743QHNSC1
p.T1441NLUAD1
p.S1004YLUAD1
p.Y700NCESC1
p.R1276HDLBC1
p.V526ABRCA1
p.Q163RLUAD1
p.C231SLUAD1
p.G610DTHYM1
p.A33TPRAD1
p.D1270HSKCM1
p.E1175*CHOL1
p.R1376CSTAD1
p.F849LBLCA1
p.D1162NSKCM1
p.V617LTHCA1
p.Y1105*LUAD1
p.S225FSKCM1
p.S117FLUAD1
p.D1251NPAAD1
p.L1357FSKCM1
p.D252NSKCM1
p.Q710*SKCM1
p.A1006VPRAD1
p.N264SSKCM1
p.P1010RLUAD1
p.R681XSKCM1
p.F473IPRAD1
p.Q59KHNSC1
p.H1213QSKCM1
p.R1402WSKCM1
p.E1426XTHYM1
p.K453NREAD1
p.R692TBLCA1
p.R1011LSKCM1
p.A61TUCEC1
p.H332RUCEC1
p.G873VLIHC1
p.E997KSKCM1
p.V409IGBM1
p.H872QUCEC1
p.S991PSKCM1
p.P314SSKCM1
p.E838KSKCM1
p.T1164KLUAD1
p.G483VUCS1
p.W372*SKCM1
p.V1090ACOAD1
p.R52QSKCM1
p.R1022CLIHC1
p.A1395VHNSC1
p.V1444ISKCM1
p.S1330NPAAD1
p.M653ISKCM1
p.D1364NSKCM1
p.A33TCOAD1
p.R1159HSTAD1
p.R846CSTAD1
p.M564IKIRC1
p.L72QLUAD1
p.A1409VHNSC1
p.K881TBLCA1
p.E1123XPRAD1
p.M915ISKCM1
p.R291GLUSC1
p.I222MBRCA1
p.P435SESCA1
p.G1226DSTAD1
p.P770LHNSC1
p.G1326DSKCM1
p.T84MSTAD1
p.R695QDLBC1
p.R681XREAD1
p.T888MSTAD1
p.T1104NSKCM1
p.T474AREAD1
p.R1022HREAD1
p.R1316KSKCM1
p.W343*BLCA1
p.G250RPRAD1
p.S905FSKCM1
p.R586ICOAD1
p.A643SLUAD1
p.N587YSKCM1
p.S890YSKCM1
p.H128DKIRP1
p.M74ISKCM1
p.R1452CGBM1
p.A26VLUAD1
p.P1307LSKCM1
p.R19CLUAD1
p.K707TSTAD1
p.R1276CSKCM1
p.N1244SSKCM1
p.V419MHNSC1
p.L608PSKCM1
p.T1069MLUAD1
p.L51VHNSC1
p.D398NSKCM1
p.P1148SSKCM1
p.R1206*OV1
p.F637LSKCM1
p.D973YPRAD1
p.L1313FSTAD1
p.E50KREAD1
p.V187ISTAD1
p.K346TUCEC1
p.T759NLUSC1
p.D114NSKCM1
p.L565MUCEC1
p.L411MSTAD1
p.D1350NSKCM1
p.E235KHNSC1
p.S511LSKCM1
p.P581LSKCM1
p.P622SSKCM1
p.G1161RSKCM1
p.P140LGBM1
p.V1000MLUAD1
p.G1338RSKCM1
p.E877KTHCA1
p.G583RSKCM1
p.D88NREAD1
p.R504WGBM1
p.C87FLUAD1
p.K721QSKCM1
p.D78NSKCM1
p.V417IKIRC1
p.D294NSKCM1
p.Q218KLUSC1
p.G1243VBLCA1
p.S1308PSTAD1
p.E400KSKCM1
p.S209FSKCM1
p.T1069MGBM1
p.V440IHNSC1
p.R1318QGBM1
p.S1393FSKCM1
p.G712ESKCM1
p.P1142TLUAD1
p.I1286SUCEC1
p.G498DSKCM1
p.D347YUCEC1
p.R1022HUCEC1
p.E315DSTAD1
p.R1114TBLCA1
p.M450IHNSC1
p.D855HLUSC1
p.G56VLIHC1
p.L248FSKCM1
p.T995MUCEC1
p.P401LGBM1
p.L794MPAAD1
p.W1014LLUAD1
p.E962KCOAD1
p.T8NKIRP1
p.F524VSTAD1
p.E656VLUAD1
p.M910ISKCM1
p.S468FSKCM1
p.P435SLUAD1
p.E182KSKCM1
p.S580CLUAD1
p.G596ESKCM1
p.V529LBRCA1
p.D207NSKCM1
p.S1025LSKCM1
p.V109IPRAD1
p.S1425WHNSC1
p.P1199LSKCM1
p.A727TLUSC1
p.E1123*PRAD1
p.R1159CUCEC1
p.P1150HLUAD1
p.L246ILUAD1
p.G322WBRCA1
p.D937NSKCM1
p.P1113LLUAD1
p.R1288HCOAD1
p.A388TUCEC1
p.S556FSKCM1
p.F524LBRCA1
p.E289KSKCM1
p.K1189NLUAD1
p.P1132SSKCM1
p.P401LSKCM1
p.P1074SUCEC1
p.R1022LPRAD1
p.W609RLUAD1
p.S1110LLGG1
p.M1457ISKCM1
p.S1410LSKCM1
p.R1169WTHYM1
p.T1064MGBM1
p.E1461KSKCM1
p.T1262SPRAD1
p.Q1289HSKCM1
p.S1425LUCEC1
p.S1027FSKCM1
p.Q1394LLUAD1
p.M932ISKCM1
p.L1052ILUAD1
p.R504LLIHC1
p.S395TLUAD1
p.E1125*LUAD1
p.L796HGBM1
p.R1067WLUSC1
p.C1236*UCEC1
p.V617GLUAD1
p.Y1411DSKCM1
p.W372RCOAD1
p.D103NSKCM1
p.R1169QUCEC1
p.P31SSKCM1
p.M705IBLCA1
p.P1392LSKCM1
p.N491KLUAD1
p.R1067WBRCA1
p.Q811LLUSC1
p.G602ESKCM1
p.S1390LSKCM1
p.R1009KSKCM1
p.D139NSKCM1
p.R1452HCOAD1
p.R1288CCOAD1
p.E953QSKCM1
p.L464PSTAD1
p.R1114TLUAD1
p.P1442SSKCM1
p.A414TLUAD1
p.A643GLUAD1
p.K1107ECESC1
p.W843XSKCM1
p.S1425LSKCM1
p.D776NUCEC1
p.I605VCOAD1
p.G532EOV1
p.R1159CLUAD1
p.N1294KLUSC1
p.D855NUCEC1
p.D105EBRCA1
p.E962KLUSC1
p.W843*SKCM1
p.Q106*SKCM1
p.P1095HBRCA1
p.G297VLUSC1
p.A638TUCEC1
p.K488*SKCM1
p.A1039EHNSC1
p.G723WLUAD1
p.P273LSKCM1
p.V1145MBLCA1
p.L1343IUCEC1
p.R181MKIRP1
p.M331ILUAD1
p.L512FLUAD1
p.E373KSKCM1
p.K309NPRAD1
p.A643TLUAD1
p.Q503PLGG1
p.L1391VCOAD1
p.R1241QCOAD1
p.R1309QCESC1
p.S677FSKCM1
p.L477FSKCM1
p.E58KCOAD1
p.W634RSKCM1
p.S511LREAD1
p.V46MDLBC1
p.R1376SLUAD1
p.D776YCOAD1
p.A1037TCOAD1
p.Q163KLUAD1
p.V419MSTAD1
p.G624AHNSC1
p.G20CLUAD1
p.R1353KSKCM1
p.E1040DPRAD1
p.G939VCOAD1
p.K309TLUAD1
p.S1425LCESC1
p.R1452HLUAD1
p.S1020YBLCA1
p.A1037TESCA1
p.V70LLUAD1
p.D462NSKCM1
p.P79SSKCM1
p.V109ISARC1
p.K1005NPAAD1
p.A37VPAAD1
p.R1042KSKCM1
p.R856WPAAD1
p.R1022CUCEC1
p.F841LLIHC1
p.I442MHNSC1
p.K488XSKCM1
p.G591RSKCM1
p.S666GUCEC1
p.D1237NSKCM1
p.E448KHNSC1
p.L307VBLCA1
p.T1408MLGG1
p.V506FLUSC1
p.K484MSKCM1
p.Q971RKIRP1
p.R681*SKCM1
p.D933NSKCM1
p.F439ISKCM1
p.Q671KSARC1
p.N709ISKCM1
p.A1261VESCA1
p.L1052FSKCM1
p.R1022CHNSC1
p.H1278YSKCM1
p.E1175KBRCA1
p.T850MSTAD1
p.R1402WREAD1
p.R1206*UCEC1
p.E427KSKCM1
p.N68HSTAD1
p.Y943CSTAD1
p.I461FLUSC1
p.S43NUCEC1
p.R1306MHNSC1
p.S616FSKCM1
p.Y1439*LUSC1
p.P883SSKCM1
p.V430ALUAD1
p.E1055KSKCM1
p.A1276VUCEC1
p.T1212KLUSC1
p.R586KSKCM1
p.P1171SSKCM1
p.N380DUCEC1
p.K1083TSKCM1
p.N992TOV1
p.P1279SSKCM1
p.K1078TESCA1
p.R695WSKCM1
p.W606*BRCA1
p.H1200QLUAD1
p.D78NREAD1
p.R846HUCEC1
p.E371DUCEC1
p.M560ISKCM1
p.D1297NLGG1
p.L735MSKCM1
p.D916NSKCM1
p.M1221ILUAD1
p.R846SLUSC1
p.L845VSTAD1
p.R1288HSKCM1
p.K394NUVM1
p.R1288HGBM1
p.A733TLIHC1


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TissGeneCNV for GRIN2A

check button Copy number variations of TissGene across 28 cancer types (X-axis: cancer type and Y-axis: % of CNV samples)
(TCGA Gistic2_CopyNumber_Gistic2_all_data_by_genes, Gistic2 copy number data, version 2016-08-16)
CNV


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TissGeneFusions for GRIN2A

check button Fusion genes including TissGene
(ChimerDB 3.0, 2016-12-01 and TCGA fusion Portal 2015-12-01)
DatabaseSrcCancer typeSampleFusion geneORF5'-gene BP3'-gene BP
Chimerdb3.0ChiTaRsNABP251842GRIN2A-GRIN2Achr16:9857658chr16:10032166
TCGAfusionPortalPRADABLCATCGA-DK-A3IN-01ACABIN1-GRIN2AOut-of-frameChr22:24515665Chr16:9984957
TCGAfusionPortalPRADABRCATCGA-BH-A5J0-01AMOBKL1B-GRIN2AOut-of-frameChr2:74405788Chr16:9928087
TCGAfusionPortalPRADALGGTCGA-CS-5397-01ASHB-GRIN2AOut-of-frameChr9:37955880Chr16:9943818


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TissGeneNet for GRIN2A

check button Co-expressed gene networks based on protein-protein interaction data (CePIN)
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
(PINA2 ppi data)
BRCA (tumor)BRCA (normal)
GRIN2A, SRC, DLG2, DLG4, GRIN1, FYN, PTK2B, DLGAP1, IL16, DLG1, PTPN4, DLG3, GRIN3B (tumor)GRIN2A, SRC, DLG2, DLG4, GRIN1, FYN, PTK2B, DLGAP1, IL16, DLG1, PTPN4, DLG3, GRIN3B (normal)
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COAD (tumor)COAD (normal)
GRIN2A, SRC, DLG2, DLG4, GRIN1, FYN, PTK2B, DLGAP1, IL16, DLG1, PTPN4, DLG3, GRIN3B (tumor)GRIN2A, SRC, DLG2, DLG4, GRIN1, FYN, PTK2B, DLGAP1, IL16, DLG1, PTPN4, DLG3, GRIN3B (normal)
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HNSC (tumor)HNSC (normal)
GRIN2A, SRC, DLG2, DLG4, GRIN1, FYN, PTK2B, DLGAP1, IL16, DLG1, PTPN4, DLG3, GRIN3B (tumor)GRIN2A, SRC, DLG2, DLG4, GRIN1, FYN, PTK2B, DLGAP1, IL16, DLG1, PTPN4, DLG3, GRIN3B (normal)
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KICH (tumor)KICH (normal)
GRIN2A, SRC, DLG2, DLG4, GRIN1, FYN, PTK2B, DLGAP1, IL16, DLG1, PTPN4, DLG3, GRIN3B (tumor)GRIN2A, SRC, DLG2, DLG4, GRIN1, FYN, PTK2B, DLGAP1, IL16, DLG1, PTPN4, DLG3, GRIN3B (normal)
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KIRC (tumor)KIRC (normal)
GRIN2A, SRC, DLG2, DLG4, GRIN1, FYN, PTK2B, DLGAP1, IL16, DLG1, PTPN4, DLG3, GRIN3B (tumor)GRIN2A, SRC, DLG2, DLG4, GRIN1, FYN, PTK2B, DLGAP1, IL16, DLG1, PTPN4, DLG3, GRIN3B (normal)
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KIRP (tumor)KIRP (normal)
GRIN2A, SRC, DLG2, DLG4, GRIN1, FYN, PTK2B, DLGAP1, IL16, DLG1, PTPN4, DLG3, GRIN3B (tumor)GRIN2A, SRC, DLG2, DLG4, GRIN1, FYN, PTK2B, DLGAP1, IL16, DLG1, PTPN4, DLG3, GRIN3B (normal)
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LIHC (tumor)LIHC (normal)
GRIN2A, SRC, DLG2, DLG4, GRIN1, FYN, PTK2B, DLGAP1, IL16, DLG1, PTPN4, DLG3, GRIN3B (tumor)GRIN2A, SRC, DLG2, DLG4, GRIN1, FYN, PTK2B, DLGAP1, IL16, DLG1, PTPN4, DLG3, GRIN3B (normal)
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LUAD (tumor)LUAD (normal)
GRIN2A, SRC, DLG2, DLG4, GRIN1, FYN, PTK2B, DLGAP1, IL16, DLG1, PTPN4, DLG3, GRIN3B (tumor)GRIN2A, SRC, DLG2, DLG4, GRIN1, FYN, PTK2B, DLGAP1, IL16, DLG1, PTPN4, DLG3, GRIN3B (normal)
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LUSC (tumor)LUSC (normal)
GRIN2A, SRC, DLG2, DLG4, GRIN1, FYN, PTK2B, DLGAP1, IL16, DLG1, PTPN4, DLG3, GRIN3B (tumor)GRIN2A, SRC, DLG2, DLG4, GRIN1, FYN, PTK2B, DLGAP1, IL16, DLG1, PTPN4, DLG3, GRIN3B (normal)
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PRAD (tumor)PRAD (normal)
GRIN2A, SRC, DLG2, DLG4, GRIN1, FYN, PTK2B, DLGAP1, IL16, DLG1, PTPN4, DLG3, GRIN3B (tumor)GRIN2A, SRC, DLG2, DLG4, GRIN1, FYN, PTK2B, DLGAP1, IL16, DLG1, PTPN4, DLG3, GRIN3B (normal)
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STAD (tumor)STAD (normal)
GRIN2A, SRC, DLG2, DLG4, GRIN1, FYN, PTK2B, DLGAP1, IL16, DLG1, PTPN4, DLG3, GRIN3B (tumor)GRIN2A, SRC, DLG2, DLG4, GRIN1, FYN, PTK2B, DLGAP1, IL16, DLG1, PTPN4, DLG3, GRIN3B (normal)
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THCA (tumor)THCA (normal)
GRIN2A, SRC, DLG2, DLG4, GRIN1, FYN, PTK2B, DLGAP1, IL16, DLG1, PTPN4, DLG3, GRIN3B (tumor)GRIN2A, SRC, DLG2, DLG4, GRIN1, FYN, PTK2B, DLGAP1, IL16, DLG1, PTPN4, DLG3, GRIN3B (normal)
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TissGeneProg for GRIN2A

check button Kaplan-Meier plots with logrank tests of overall survival (OS) using 28 cancer types
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
(TCGA clinicalMatrix, phenotype data, version 2016-04-27)

* Click on the image to enlarge it in a new window.
survival 1

check button Kaplan-Meier plots with logrank test of relapse free survival (RFS) using 28 cancer types
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
(TCGA clinicalMatrix, phenotype data, version 2016-04-27)

* Click on the image enlarge it in a new window.
survival 2

check button Forest plot of Cox proportional hazard ratio (HR) and 95% CI of overall survival (OS) using 28 cancer types
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
(TCGA clinicalMatrix, phenotype data, version 2016-04-27)

* Click on the image enlarge it in a new window.
survival 3

check button Forest plot of Cox proportional hazard ratio (HR) and 95% CI of relapse free survival (RFS) using 28 cancer types
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
(TCGA clinicalMatrix, phenotype data, version 2016-04-27)

* Click on the image enlarge it in a new window.
survival 4

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TissGeneClin for GRIN2A
TissGeneDrug for GRIN2A

check button Drug information targeting TissGene
(DrugBank Version 5.0.6, 2017-04-01)
DrugBank IDDrug nameDrug activityDrug typeDrug status
DB00454PethidineAntagonistSmall moleculeApproved
DB00949FelbamateAntagonistSmall moleculeApproved
DB06151AcetylcysteineActivatorSmall moleculeApproved


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TissGeneDisease for GRIN2A

check button Disease information associated with TissGene
(DisGeNet, 2016-06-01)
Disease IDDisease name# pubmedsSource
umls:C0036341Schizophrenia18BeFree,GAD,GWASCAT,LHGDN
umls:C0014544Epilepsy12BeFree,CTD_human
umls:C0005586Bipolar Disorder9BeFree,GAD
umls:C3806402EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION7ORPHANET,UNIPROT
umls:C1263846Attention deficit hyperactivity disorder5BeFree,GAD
umls:C0041696Unipolar Depression4BeFree
umls:C0376532Epilepsy, Rolandic4BeFree,CTD_human
umls:C1096063Drug Resistant Epilepsy4BeFree
umls:C1269683Major Depressive Disorder4BeFree
umls:C0001973Alcoholic Intoxication, Chronic3BeFree,GAD
umls:C0020179Huntington Disease3BeFree,GAD,LHGDN
umls:C0002395Alzheimer's Disease2BeFree,LHGDN
umls:C0002736Amyotrophic Lateral Sclerosis2BeFree,GAD
umls:C0004936Mental disorders2BeFree,GAD
umls:C0014547Epilepsies, Partial2BeFree
umls:C0019337Heroin Dependence2BeFree
umls:C0023890Liver Cirrhosis2BeFree
umls:C0025202melanoma2BeFree,CTD_human
umls:C0085584Encephalopathies2BeFree
umls:C0525045Mood Disorders2BeFree
umls:C0751495Seizures, Focal2BeFree
umls:C1623038Cirrhosis2BeFree
umls:C3714756Intellectual Disability2BeFree
umls:C3806403CONTINUOUS SPIKE AND WAVES DURING SLOW-WAVE SLEEP SYNDROME2BeFree
umls:C0003537Aphasia1BeFree
umls:C0003635Apraxias1BeFree
umls:C0004352Autistic Disorder1BeFree,CTD_human
umls:C0007102Malignant tumor of colon1BeFree
umls:C0009402Colorectal Carcinoma1BeFree
umls:C0009404Colorectal Neoplasms1CTD_human,LHGDN
umls:C0011570Mental Depression1BeFree
umls:C0011581Depressive disorder1BeFree
umls:C0013170Drug habituation1BeFree
umls:C0013362Dysarthria1BeFree
umls:C0014556Epilepsy, Temporal Lobe1BeFree
umls:C0015934Fetal Growth Retardation1RGD
umls:C0018817Atrial Septal Defects1BeFree
umls:C0019163Hepatitis B1BeFree,GAD,GWASCAT
umls:C0022116Ischemia1BeFree
umls:C0023014Language Development Disorders1CTD_human
umls:C0025362Mental Retardation1BeFree
umls:C0026552Morphine Dependence1CTD_human
umls:C0027404Narcolepsy1GAD
umls:C0032051Placental Insufficiency1RGD
umls:C0033975Psychotic Disorders1BeFree
umls:C0035126Reperfusion Injury1RGD
umls:C0036572Seizures1BeFree
umls:C0037769West Syndrome1BeFree
umls:C0037822Speech Disorders1CTD_human
umls:C0038220Status Epilepticus1BeFree
umls:C0038454Cerebrovascular accident1BeFree
umls:C0038587Substance Withdrawal Syndrome1CTD_human
umls:C0040336Tobacco Use Disorder1GAD
umls:C0041107Trisomy1BeFree
umls:C0043094Weight Gain1GAD
umls:C0085400Neurofibrillary degeneration (morphologic abnormality)1BeFree
umls:C0206716Ganglioglioma1BeFree
umls:C0233715Speech impairment1BeFree
umls:C0234516Speech dysfunction1BeFree
umls:C0243026Sepsis1RGD
umls:C0282512Landau-Kleffner Syndrome1BeFree,CTD_human,ORPHANET
umls:C0348165Central Nervous System Viral Diseases1RGD
umls:C0349204Nonorganic psychosis1BeFree
umls:C0424605Developmental delay (disorder)1BeFree
umls:C0524662Opiate Addiction1BeFree
umls:C0678356alcohol effect1BeFree
umls:C0699790Colon Carcinoma1BeFree
umls:C0752308Hypoxia-Ischemia, Brain1RGD
umls:C1504404Hippocampal sclerosis1BeFree
umls:C1868677PHOTOPAROXYSMAL RESPONSE 11BeFree
umls:C2911647Weight Gain Adverse Event1GAD
umls:C1832814Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, Autosomal Dominant0CLINVAR