TissGeneSummary for GRIN2A |
Gene summary |
Basic gene information | Gene symbol | GRIN2A |
Gene name | glutamate receptor, ionotropic, N-methyl D-aspartate 2A | |
Synonyms | EPND|FESD|GluN2A|LKS|NMDAR2A|NR2A | |
Cytomap | UCSC genome browser: 16p13.2 | |
Type of gene | protein-coding | |
RefGenes | NM_000833.4, NM_001134407.2,NM_001134408.2, | |
Description | N-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 date | 20141222 | |
dbXrefs | MIM : 138253 | |
HGNC : HGNC | ||
Ensembl : ENSG00000183454 | ||
HPRD : 00698 | ||
Vega : OTTHUMG00000129721 | ||
Protein | UniProt: go to UniProt's Cross Reference DB Table | |
Expression | CleanEX: HS_GRIN2A | |
BioGPS: 2903 | ||
Pathway | NCI Pathway Interaction Database: GRIN2A | |
KEGG: GRIN2A | ||
REACTOME: GRIN2A | ||
Pathway Commons: GRIN2A | ||
Context | iHOP: GRIN2A | |
ligand binding site mutation search in PubMed: GRIN2A | ||
UCL Cancer Institute: GRIN2A | ||
Assigned class in TissGDB* | C | |
Included tissue-specific gene expression resources | HPA,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 annotations | Cancer 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. |
Gene ontology having evidence of Inferred from Direct Assay (IDA) from Entrez |
GO ID | GO term | PubMed ID | GO:0045471 | response to ethanol | 18445116 | GO:0045471 | response to ethanol | 18445116 |
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TissGeneExp for GRIN2A |
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 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 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. |
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) |
- Significantly differentially expressed cancer types and information. (|Fold change|>1 and FDR<0.05) |
Cancer type | Mean(exp) in tumor | Mean(exp) in matched normal | Log2FC | P-val. | FDR |
KIRP | -0.611847619 | 2.186996131 | -2.79884375 | 7.82E-09 | 6.09E-08 |
BRCA | 0.683782425 | 2.119683302 | -1.435900877 | 1.09E-12 | 4.87E-12 |
COAD | -2.066158196 | 0.931714881 | -2.997873077 | 1.36E-13 | 4.45E-12 |
STAD | 1.238380506 | 3.807883631 | -2.569503125 | 8.09E-07 | 1.37E-05 |
KICH | 0.177762881 | 1.523222881 | -1.34546 | 0.0198 | 0.033491328 |
LIHC | -0.688159119 | -1.968451119 | 1.280292 | 0.0057 | 0.012931256 |
ESCA | -0.00939421 | 3.668923972 | -3.678318182 | 0.000793 | 0.012508028 |
PRAD | -0.123963965 | 0.989697573 | -1.113661538 | 3.16E-05 | 0.000151965 |
BLCA | -1.989474593 | 0.933656986 | -2.923131579 | 5.76E-06 | 0.000125591 |
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TissGene-miRNA for GRIN2A |
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 type | miRNA id | miRNA accession | P-val. | Coeff. | # samples |
LUAD | hsa-miR-27b-3p | MIMAT0000419 | 0.034 | -0.28 | 60 |
UVM | hsa-miR-30b-5p | MIMAT0000420 | 0.012 | -0.28 | 80 |
ACC | hsa-miR-373-3p | MIMAT0000726 | 0.0099 | -0.29 | 78 |
ACC | hsa-miR-373-3p | MIMAT0000726 | 0.0099 | -0.29 | 78 |
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TissGeneMut for GRIN2A |
TissGeneSNV for GRIN2A |
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. |
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) |
- nsSNVs sorted by frequency. |
AAchange | Cancer type | # samples |
p.G1322E | SKCM | 7 |
p.E962K | SKCM | 3 |
p.R1067W | SKCM | 3 |
p.D1153N | SKCM | 3 |
p.G688E | SKCM | 3 |
p.G20D | SKCM | 2 |
p.E1175K | SKCM | 2 |
p.R1022C | LUAD | 2 |
p.R1067Q | SKCM | 2 |
p.D105N | SKCM | 2 |
p.R1376C | BLCA | 2 |
p.D1315N | SKCM | 2 |
p.S1447F | SKCM | 2 |
p.P699S | SKCM | 2 |
p.E806K | SKCM | 2 |
p.D1024N | SKCM | 2 |
p.D344N | SKCM | 2 |
p.E657K | SKCM | 2 |
p.E1156K | SKCM | 2 |
p.P1132L | SKCM | 2 |
p.E743K | SKCM | 2 |
p.P273S | SKCM | 2 |
p.E1125K | SKCM | 2 |
p.E1073K | SKCM | 2 |
p.H1129Y | SKCM | 2 |
p.D731N | SKCM | 1 |
p.R370Q | SKCM | 1 |
p.R1241Q | LUSC | 1 |
p.D78N | UCS | 1 |
p.M817I | STAD | 1 |
p.E1175X | CHOL | 1 |
p.G101R | SKCM | 1 |
p.A968P | LUAD | 1 |
p.N946S | SKCM | 1 |
p.Q1278K | KIRC | 1 |
p.A302T | COAD | 1 |
p.P401Q | LUAD | 1 |
p.G1127C | BLCA | 1 |
p.R970W | UCEC | 1 |
p.D234N | SKCM | 1 |
p.H381Y | SKCM | 1 |
p.A643S | HNSC | 1 |
p.D1195E | HNSC | 1 |
p.V568F | LUAD | 1 |
p.N490Y | LGG | 1 |
p.M133I | SKCM | 1 |
p.G873E | HNSC | 1 |
p.A638T | COAD | 1 |
p.A921T | LGG | 1 |
p.S1403L | SKCM | 1 |
p.V633A | BLCA | 1 |
p.S1045F | SKCM | 1 |
p.E743Q | HNSC | 1 |
p.T1441N | LUAD | 1 |
p.S1004Y | LUAD | 1 |
p.Y700N | CESC | 1 |
p.R1276H | DLBC | 1 |
p.V526A | BRCA | 1 |
p.Q163R | LUAD | 1 |
p.C231S | LUAD | 1 |
p.G610D | THYM | 1 |
p.A33T | PRAD | 1 |
p.D1270H | SKCM | 1 |
p.E1175* | CHOL | 1 |
p.R1376C | STAD | 1 |
p.F849L | BLCA | 1 |
p.D1162N | SKCM | 1 |
p.V617L | THCA | 1 |
p.Y1105* | LUAD | 1 |
p.S225F | SKCM | 1 |
p.S117F | LUAD | 1 |
p.D1251N | PAAD | 1 |
p.L1357F | SKCM | 1 |
p.D252N | SKCM | 1 |
p.Q710* | SKCM | 1 |
p.A1006V | PRAD | 1 |
p.N264S | SKCM | 1 |
p.P1010R | LUAD | 1 |
p.R681X | SKCM | 1 |
p.F473I | PRAD | 1 |
p.Q59K | HNSC | 1 |
p.H1213Q | SKCM | 1 |
p.R1402W | SKCM | 1 |
p.E1426X | THYM | 1 |
p.K453N | READ | 1 |
p.R692T | BLCA | 1 |
p.R1011L | SKCM | 1 |
p.A61T | UCEC | 1 |
p.H332R | UCEC | 1 |
p.G873V | LIHC | 1 |
p.E997K | SKCM | 1 |
p.V409I | GBM | 1 |
p.H872Q | UCEC | 1 |
p.S991P | SKCM | 1 |
p.P314S | SKCM | 1 |
p.E838K | SKCM | 1 |
p.T1164K | LUAD | 1 |
p.G483V | UCS | 1 |
p.W372* | SKCM | 1 |
p.V1090A | COAD | 1 |
p.R52Q | SKCM | 1 |
p.R1022C | LIHC | 1 |
p.A1395V | HNSC | 1 |
p.V1444I | SKCM | 1 |
p.S1330N | PAAD | 1 |
p.M653I | SKCM | 1 |
p.D1364N | SKCM | 1 |
p.A33T | COAD | 1 |
p.R1159H | STAD | 1 |
p.R846C | STAD | 1 |
p.M564I | KIRC | 1 |
p.L72Q | LUAD | 1 |
p.A1409V | HNSC | 1 |
p.K881T | BLCA | 1 |
p.E1123X | PRAD | 1 |
p.M915I | SKCM | 1 |
p.R291G | LUSC | 1 |
p.I222M | BRCA | 1 |
p.P435S | ESCA | 1 |
p.G1226D | STAD | 1 |
p.P770L | HNSC | 1 |
p.G1326D | SKCM | 1 |
p.T84M | STAD | 1 |
p.R695Q | DLBC | 1 |
p.R681X | READ | 1 |
p.T888M | STAD | 1 |
p.T1104N | SKCM | 1 |
p.T474A | READ | 1 |
p.R1022H | READ | 1 |
p.R1316K | SKCM | 1 |
p.W343* | BLCA | 1 |
p.G250R | PRAD | 1 |
p.S905F | SKCM | 1 |
p.R586I | COAD | 1 |
p.A643S | LUAD | 1 |
p.N587Y | SKCM | 1 |
p.S890Y | SKCM | 1 |
p.H128D | KIRP | 1 |
p.M74I | SKCM | 1 |
p.R1452C | GBM | 1 |
p.A26V | LUAD | 1 |
p.P1307L | SKCM | 1 |
p.R19C | LUAD | 1 |
p.K707T | STAD | 1 |
p.R1276C | SKCM | 1 |
p.N1244S | SKCM | 1 |
p.V419M | HNSC | 1 |
p.L608P | SKCM | 1 |
p.T1069M | LUAD | 1 |
p.L51V | HNSC | 1 |
p.D398N | SKCM | 1 |
p.P1148S | SKCM | 1 |
p.R1206* | OV | 1 |
p.F637L | SKCM | 1 |
p.D973Y | PRAD | 1 |
p.L1313F | STAD | 1 |
p.E50K | READ | 1 |
p.V187I | STAD | 1 |
p.K346T | UCEC | 1 |
p.T759N | LUSC | 1 |
p.D114N | SKCM | 1 |
p.L565M | UCEC | 1 |
p.L411M | STAD | 1 |
p.D1350N | SKCM | 1 |
p.E235K | HNSC | 1 |
p.S511L | SKCM | 1 |
p.P581L | SKCM | 1 |
p.P622S | SKCM | 1 |
p.G1161R | SKCM | 1 |
p.P140L | GBM | 1 |
p.V1000M | LUAD | 1 |
p.G1338R | SKCM | 1 |
p.E877K | THCA | 1 |
p.G583R | SKCM | 1 |
p.D88N | READ | 1 |
p.R504W | GBM | 1 |
p.C87F | LUAD | 1 |
p.K721Q | SKCM | 1 |
p.D78N | SKCM | 1 |
p.V417I | KIRC | 1 |
p.D294N | SKCM | 1 |
p.Q218K | LUSC | 1 |
p.G1243V | BLCA | 1 |
p.S1308P | STAD | 1 |
p.E400K | SKCM | 1 |
p.S209F | SKCM | 1 |
p.T1069M | GBM | 1 |
p.V440I | HNSC | 1 |
p.R1318Q | GBM | 1 |
p.S1393F | SKCM | 1 |
p.G712E | SKCM | 1 |
p.P1142T | LUAD | 1 |
p.I1286S | UCEC | 1 |
p.G498D | SKCM | 1 |
p.D347Y | UCEC | 1 |
p.R1022H | UCEC | 1 |
p.E315D | STAD | 1 |
p.R1114T | BLCA | 1 |
p.M450I | HNSC | 1 |
p.D855H | LUSC | 1 |
p.G56V | LIHC | 1 |
p.L248F | SKCM | 1 |
p.T995M | UCEC | 1 |
p.P401L | GBM | 1 |
p.L794M | PAAD | 1 |
p.W1014L | LUAD | 1 |
p.E962K | COAD | 1 |
p.T8N | KIRP | 1 |
p.F524V | STAD | 1 |
p.E656V | LUAD | 1 |
p.M910I | SKCM | 1 |
p.S468F | SKCM | 1 |
p.P435S | LUAD | 1 |
p.E182K | SKCM | 1 |
p.S580C | LUAD | 1 |
p.G596E | SKCM | 1 |
p.V529L | BRCA | 1 |
p.D207N | SKCM | 1 |
p.S1025L | SKCM | 1 |
p.V109I | PRAD | 1 |
p.S1425W | HNSC | 1 |
p.P1199L | SKCM | 1 |
p.A727T | LUSC | 1 |
p.E1123* | PRAD | 1 |
p.R1159C | UCEC | 1 |
p.P1150H | LUAD | 1 |
p.L246I | LUAD | 1 |
p.G322W | BRCA | 1 |
p.D937N | SKCM | 1 |
p.P1113L | LUAD | 1 |
p.R1288H | COAD | 1 |
p.A388T | UCEC | 1 |
p.S556F | SKCM | 1 |
p.F524L | BRCA | 1 |
p.E289K | SKCM | 1 |
p.K1189N | LUAD | 1 |
p.P1132S | SKCM | 1 |
p.P401L | SKCM | 1 |
p.P1074S | UCEC | 1 |
p.R1022L | PRAD | 1 |
p.W609R | LUAD | 1 |
p.S1110L | LGG | 1 |
p.M1457I | SKCM | 1 |
p.S1410L | SKCM | 1 |
p.R1169W | THYM | 1 |
p.T1064M | GBM | 1 |
p.E1461K | SKCM | 1 |
p.T1262S | PRAD | 1 |
p.Q1289H | SKCM | 1 |
p.S1425L | UCEC | 1 |
p.S1027F | SKCM | 1 |
p.Q1394L | LUAD | 1 |
p.M932I | SKCM | 1 |
p.L1052I | LUAD | 1 |
p.R504L | LIHC | 1 |
p.S395T | LUAD | 1 |
p.E1125* | LUAD | 1 |
p.L796H | GBM | 1 |
p.R1067W | LUSC | 1 |
p.C1236* | UCEC | 1 |
p.V617G | LUAD | 1 |
p.Y1411D | SKCM | 1 |
p.W372R | COAD | 1 |
p.D103N | SKCM | 1 |
p.R1169Q | UCEC | 1 |
p.P31S | SKCM | 1 |
p.M705I | BLCA | 1 |
p.P1392L | SKCM | 1 |
p.N491K | LUAD | 1 |
p.R1067W | BRCA | 1 |
p.Q811L | LUSC | 1 |
p.G602E | SKCM | 1 |
p.S1390L | SKCM | 1 |
p.R1009K | SKCM | 1 |
p.D139N | SKCM | 1 |
p.R1452H | COAD | 1 |
p.R1288C | COAD | 1 |
p.E953Q | SKCM | 1 |
p.L464P | STAD | 1 |
p.R1114T | LUAD | 1 |
p.P1442S | SKCM | 1 |
p.A414T | LUAD | 1 |
p.A643G | LUAD | 1 |
p.K1107E | CESC | 1 |
p.W843X | SKCM | 1 |
p.S1425L | SKCM | 1 |
p.D776N | UCEC | 1 |
p.I605V | COAD | 1 |
p.G532E | OV | 1 |
p.R1159C | LUAD | 1 |
p.N1294K | LUSC | 1 |
p.D855N | UCEC | 1 |
p.D105E | BRCA | 1 |
p.E962K | LUSC | 1 |
p.W843* | SKCM | 1 |
p.Q106* | SKCM | 1 |
p.P1095H | BRCA | 1 |
p.G297V | LUSC | 1 |
p.A638T | UCEC | 1 |
p.K488* | SKCM | 1 |
p.A1039E | HNSC | 1 |
p.G723W | LUAD | 1 |
p.P273L | SKCM | 1 |
p.V1145M | BLCA | 1 |
p.L1343I | UCEC | 1 |
p.R181M | KIRP | 1 |
p.M331I | LUAD | 1 |
p.L512F | LUAD | 1 |
p.E373K | SKCM | 1 |
p.K309N | PRAD | 1 |
p.A643T | LUAD | 1 |
p.Q503P | LGG | 1 |
p.L1391V | COAD | 1 |
p.R1241Q | COAD | 1 |
p.R1309Q | CESC | 1 |
p.S677F | SKCM | 1 |
p.L477F | SKCM | 1 |
p.E58K | COAD | 1 |
p.W634R | SKCM | 1 |
p.S511L | READ | 1 |
p.V46M | DLBC | 1 |
p.R1376S | LUAD | 1 |
p.D776Y | COAD | 1 |
p.A1037T | COAD | 1 |
p.Q163K | LUAD | 1 |
p.V419M | STAD | 1 |
p.G624A | HNSC | 1 |
p.G20C | LUAD | 1 |
p.R1353K | SKCM | 1 |
p.E1040D | PRAD | 1 |
p.G939V | COAD | 1 |
p.K309T | LUAD | 1 |
p.S1425L | CESC | 1 |
p.R1452H | LUAD | 1 |
p.S1020Y | BLCA | 1 |
p.A1037T | ESCA | 1 |
p.V70L | LUAD | 1 |
p.D462N | SKCM | 1 |
p.P79S | SKCM | 1 |
p.V109I | SARC | 1 |
p.K1005N | PAAD | 1 |
p.A37V | PAAD | 1 |
p.R1042K | SKCM | 1 |
p.R856W | PAAD | 1 |
p.R1022C | UCEC | 1 |
p.F841L | LIHC | 1 |
p.I442M | HNSC | 1 |
p.K488X | SKCM | 1 |
p.G591R | SKCM | 1 |
p.S666G | UCEC | 1 |
p.D1237N | SKCM | 1 |
p.E448K | HNSC | 1 |
p.L307V | BLCA | 1 |
p.T1408M | LGG | 1 |
p.V506F | LUSC | 1 |
p.K484M | SKCM | 1 |
p.Q971R | KIRP | 1 |
p.R681* | SKCM | 1 |
p.D933N | SKCM | 1 |
p.F439I | SKCM | 1 |
p.Q671K | SARC | 1 |
p.N709I | SKCM | 1 |
p.A1261V | ESCA | 1 |
p.L1052F | SKCM | 1 |
p.R1022C | HNSC | 1 |
p.H1278Y | SKCM | 1 |
p.E1175K | BRCA | 1 |
p.T850M | STAD | 1 |
p.R1402W | READ | 1 |
p.R1206* | UCEC | 1 |
p.E427K | SKCM | 1 |
p.N68H | STAD | 1 |
p.Y943C | STAD | 1 |
p.I461F | LUSC | 1 |
p.S43N | UCEC | 1 |
p.R1306M | HNSC | 1 |
p.S616F | SKCM | 1 |
p.Y1439* | LUSC | 1 |
p.P883S | SKCM | 1 |
p.V430A | LUAD | 1 |
p.E1055K | SKCM | 1 |
p.A1276V | UCEC | 1 |
p.T1212K | LUSC | 1 |
p.R586K | SKCM | 1 |
p.P1171S | SKCM | 1 |
p.N380D | UCEC | 1 |
p.K1083T | SKCM | 1 |
p.N992T | OV | 1 |
p.P1279S | SKCM | 1 |
p.K1078T | ESCA | 1 |
p.R695W | SKCM | 1 |
p.W606* | BRCA | 1 |
p.H1200Q | LUAD | 1 |
p.D78N | READ | 1 |
p.R846H | UCEC | 1 |
p.E371D | UCEC | 1 |
p.M560I | SKCM | 1 |
p.D1297N | LGG | 1 |
p.L735M | SKCM | 1 |
p.D916N | SKCM | 1 |
p.M1221I | LUAD | 1 |
p.R846S | LUSC | 1 |
p.L845V | STAD | 1 |
p.R1288H | SKCM | 1 |
p.K394N | UVM | 1 |
p.R1288H | GBM | 1 |
p.A733T | LIHC | 1 |
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TissGeneCNV for GRIN2A |
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) |
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TissGeneFusions for GRIN2A |
Fusion genes including TissGene (ChimerDB 3.0, 2016-12-01 and TCGA fusion Portal 2015-12-01) |
Database | Src | Cancer type | Sample | Fusion gene | ORF | 5'-gene BP | 3'-gene BP |
Chimerdb3.0 | ChiTaRs | NA | BP251842 | GRIN2A-GRIN2A | chr16:9857658 | chr16:10032166 | |
TCGAfusionPortal | PRADA | BLCA | TCGA-DK-A3IN-01A | CABIN1-GRIN2A | Out-of-frame | Chr22:24515665 | Chr16:9984957 |
TCGAfusionPortal | PRADA | BRCA | TCGA-BH-A5J0-01A | MOBKL1B-GRIN2A | Out-of-frame | Chr2:74405788 | Chr16:9928087 |
TCGAfusionPortal | PRADA | LGG | TCGA-CS-5397-01A | SHB-GRIN2A | Out-of-frame | Chr9:37955880 | Chr16:9943818 |
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TissGeneNet for GRIN2A |
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) |
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TissGeneProg for GRIN2A |
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. |
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. |
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. |
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. |
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TissGeneClin for GRIN2A |
TissGeneDrug for GRIN2A |
Drug information targeting TissGene (DrugBank Version 5.0.6, 2017-04-01) |
DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
DB00454 | Pethidine | Antagonist | Small molecule | Approved |
DB00949 | Felbamate | Antagonist | Small molecule | Approved |
DB06151 | Acetylcysteine | Activator | Small molecule | Approved |
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TissGeneDisease for GRIN2A |
Disease information associated with TissGene (DisGeNet, 2016-06-01) |
Disease ID | Disease name | # pubmeds | Source |
umls:C0036341 | Schizophrenia | 18 | BeFree,GAD,GWASCAT,LHGDN |
umls:C0014544 | Epilepsy | 12 | BeFree,CTD_human |
umls:C0005586 | Bipolar Disorder | 9 | BeFree,GAD |
umls:C3806402 | EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION | 7 | ORPHANET,UNIPROT |
umls:C1263846 | Attention deficit hyperactivity disorder | 5 | BeFree,GAD |
umls:C0041696 | Unipolar Depression | 4 | BeFree |
umls:C0376532 | Epilepsy, Rolandic | 4 | BeFree,CTD_human |
umls:C1096063 | Drug Resistant Epilepsy | 4 | BeFree |
umls:C1269683 | Major Depressive Disorder | 4 | BeFree |
umls:C0001973 | Alcoholic Intoxication, Chronic | 3 | BeFree,GAD |
umls:C0020179 | Huntington Disease | 3 | BeFree,GAD,LHGDN |
umls:C0002395 | Alzheimer's Disease | 2 | BeFree,LHGDN |
umls:C0002736 | Amyotrophic Lateral Sclerosis | 2 | BeFree,GAD |
umls:C0004936 | Mental disorders | 2 | BeFree,GAD |
umls:C0014547 | Epilepsies, Partial | 2 | BeFree |
umls:C0019337 | Heroin Dependence | 2 | BeFree |
umls:C0023890 | Liver Cirrhosis | 2 | BeFree |
umls:C0025202 | melanoma | 2 | BeFree,CTD_human |
umls:C0085584 | Encephalopathies | 2 | BeFree |
umls:C0525045 | Mood Disorders | 2 | BeFree |
umls:C0751495 | Seizures, Focal | 2 | BeFree |
umls:C1623038 | Cirrhosis | 2 | BeFree |
umls:C3714756 | Intellectual Disability | 2 | BeFree |
umls:C3806403 | CONTINUOUS SPIKE AND WAVES DURING SLOW-WAVE SLEEP SYNDROME | 2 | BeFree |
umls:C0003537 | Aphasia | 1 | BeFree |
umls:C0003635 | Apraxias | 1 | BeFree |
umls:C0004352 | Autistic Disorder | 1 | BeFree,CTD_human |
umls:C0007102 | Malignant tumor of colon | 1 | BeFree |
umls:C0009402 | Colorectal Carcinoma | 1 | BeFree |
umls:C0009404 | Colorectal Neoplasms | 1 | CTD_human,LHGDN |
umls:C0011570 | Mental Depression | 1 | BeFree |
umls:C0011581 | Depressive disorder | 1 | BeFree |
umls:C0013170 | Drug habituation | 1 | BeFree |
umls:C0013362 | Dysarthria | 1 | BeFree |
umls:C0014556 | Epilepsy, Temporal Lobe | 1 | BeFree |
umls:C0015934 | Fetal Growth Retardation | 1 | RGD |
umls:C0018817 | Atrial Septal Defects | 1 | BeFree |
umls:C0019163 | Hepatitis B | 1 | BeFree,GAD,GWASCAT |
umls:C0022116 | Ischemia | 1 | BeFree |
umls:C0023014 | Language Development Disorders | 1 | CTD_human |
umls:C0025362 | Mental Retardation | 1 | BeFree |
umls:C0026552 | Morphine Dependence | 1 | CTD_human |
umls:C0027404 | Narcolepsy | 1 | GAD |
umls:C0032051 | Placental Insufficiency | 1 | RGD |
umls:C0033975 | Psychotic Disorders | 1 | BeFree |
umls:C0035126 | Reperfusion Injury | 1 | RGD |
umls:C0036572 | Seizures | 1 | BeFree |
umls:C0037769 | West Syndrome | 1 | BeFree |
umls:C0037822 | Speech Disorders | 1 | CTD_human |
umls:C0038220 | Status Epilepticus | 1 | BeFree |
umls:C0038454 | Cerebrovascular accident | 1 | BeFree |
umls:C0038587 | Substance Withdrawal Syndrome | 1 | CTD_human |
umls:C0040336 | Tobacco Use Disorder | 1 | GAD |
umls:C0041107 | Trisomy | 1 | BeFree |
umls:C0043094 | Weight Gain | 1 | GAD |
umls:C0085400 | Neurofibrillary degeneration (morphologic abnormality) | 1 | BeFree |
umls:C0206716 | Ganglioglioma | 1 | BeFree |
umls:C0233715 | Speech impairment | 1 | BeFree |
umls:C0234516 | Speech dysfunction | 1 | BeFree |
umls:C0243026 | Sepsis | 1 | RGD |
umls:C0282512 | Landau-Kleffner Syndrome | 1 | BeFree,CTD_human,ORPHANET |
umls:C0348165 | Central Nervous System Viral Diseases | 1 | RGD |
umls:C0349204 | Nonorganic psychosis | 1 | BeFree |
umls:C0424605 | Developmental delay (disorder) | 1 | BeFree |
umls:C0524662 | Opiate Addiction | 1 | BeFree |
umls:C0678356 | alcohol effect | 1 | BeFree |
umls:C0699790 | Colon Carcinoma | 1 | BeFree |
umls:C0752308 | Hypoxia-Ischemia, Brain | 1 | RGD |
umls:C1504404 | Hippocampal sclerosis | 1 | BeFree |
umls:C1868677 | PHOTOPAROXYSMAL RESPONSE 1 | 1 | BeFree |
umls:C2911647 | Weight Gain Adverse Event | 1 | GAD |
umls:C1832814 | Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, Autosomal Dominant | 0 | CLINVAR |