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Phenotypic Information (metabolism pathway, cancer, disease, phenome) | |
Gene-Gene Network Information: Co-Expression Network, Interacting Genes & KEGG | |
Gene Summary for GNAO1 |
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Phenotypic Information for GNAO1(metabolism pathway, cancer, disease, phenome) |
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Cancer | CGAP: GNAO1 |
Familial Cancer Database: GNAO1 |
* This gene is included in those cancer gene databases. |
Oncogene 1 | Significant driver gene in |
cf) number; DB name 1 Oncogene; http://nar.oxfordjournals.org/content/35/suppl_1/D721.long, 2 Tumor Suppressor gene; https://bioinfo.uth.edu/TSGene/, 3 Cancer Gene Census; http://www.nature.com/nrc/journal/v4/n3/abs/nrc1299.html, 4 CancerGenes; http://nar.oxfordjournals.org/content/35/suppl_1/D721.long, 5 Network of Cancer Gene; http://ncg.kcl.ac.uk/index.php, 1Therapeutic Vulnerabilities in Cancer; http://cbio.mskcc.org/cancergenomics/statius/ |
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REACTOME_INTEGRATION_OF_ENERGY_METABOLISM |
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OMIM | |
Orphanet | |
Disease | KEGG Disease: GNAO1 |
MedGen: GNAO1 (Human Medical Genetics with Condition) | |
ClinVar: GNAO1 | |
Phenotype | MGI: GNAO1 (International Mouse Phenotyping Consortium) |
PhenomicDB: GNAO1 |
Mutations for GNAO1 |
* Under tables are showing count per each tissue to give us broad intuition about tissue specific mutation patterns.You can go to the detailed page for each mutation database's web site. |
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- Statistics for Tissue and Mutation type | Top |
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- For Inter-chromosomal Variations |
There's no inter-chromosomal structural variation. |
- For Intra-chromosomal Variations |
* Intra-chromosomal variantions includes 'intrachromosomal amplicon to amplicon', 'intrachromosomal amplicon to non-amplified dna', 'intrachromosomal deletion', 'intrachromosomal fold-back inversion', 'intrachromosomal inversion', 'intrachromosomal tandem duplication', 'Intrachromosomal unknown type', 'intrachromosomal with inverted orientation', 'intrachromosomal with non-inverted orientation'. |
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Sample | Symbol_a | Chr_a | Start_a | End_a | Symbol_b | Chr_b | Start_b | End_b |
breast | GNAO1 | chr16 | 56232647 | 56232647 | GNAO1 | chr16 | 56252900 | 56252900 |
large_intestine | GNAO1 | chr16 | 56312514 | 56312514 | chr16 | 79703505 | 79703505 |
cf) Tissue number; Tissue name (1;Breast, 2;Central_nervous_system, 3;Haematopoietic_and_lymphoid_tissue, 4;Large_intestine, 5;Liver, 6;Lung, 7;Ovary, 8;Pancreas, 9;Prostate, 10;Skin, 11;Soft_tissue, 12;Upper_aerodigestive_tract) |
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* From mRNA Sanger sequences, Chitars2.0 arranged chimeric transcripts. This table shows GNAO1 related fusion information. |
ID | Head Gene | Tail Gene | Accession | Gene_a | qStart_a | qEnd_a | Chromosome_a | tStart_a | tEnd_a | Gene_a | qStart_a | qEnd_a | Chromosome_a | tStart_a | tEnd_a |
DB344809 | FBRSL1 | 1 | 64 | 12 | 133160815 | 133160878 | GNAO1 | 59 | 550 | 16 | 56374478 | 56377743 | |
DA491290 | ZNF711 | 1 | 126 | X | 84498997 | 84499122 | GNAO1 | 125 | 553 | 16 | 56225702 | 56226130 | |
BF362557 | TBC1D5 | 2 | 74 | 3 | 17780626 | 17780698 | GNAO1 | 71 | 328 | 16 | 56378567 | 56378824 | |
AW014453 | GNAO1 | 11 | 61 | 16 | 56390199 | 56390249 | GNAO1 | 54 | 393 | 16 | 56389963 | 56390302 | |
M78823 | GNAO1 | 1 | 89 | 16 | 56390777 | 56390865 | FAM81A | 83 | 441 | 15 | 59732524 | 59732880 |
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Mutation type/ Tissue ID | brca | cns | cerv | endome | haematopo | kidn | Lintest | liver | lung | ns | ovary | pancre | prost | skin | stoma | thyro | urina | |||
Total # sample |   |   |   |   |   |   | 1 |   |   |   |   |   |   |   |   |   |   | |||
GAIN (# sample) |   |   |   |   |   |   |   |   |   |   |   |   |   |   |   |   |   | |||
LOSS (# sample) |   |   |   |   |   |   | 1 |   |   |   |   |   |   |   |   |   |   |
cf) Tissue ID; Tissue type (1; Breast, 2; Central_nervous_system, 3; Cervix, 4; Endometrium, 5; Haematopoietic_and_lymphoid_tissue, 6; Kidney, 7; Large_intestine, 8; Liver, 9; Lung, 10; NS, 11; Ovary, 12; Pancreas, 13; Prostate, 14; Skin, 15; Stomach, 16; Thyroid, 17; Urinary_tract) |
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Stat. for Non-Synonymous SNVs (# total SNVs=33) | (# total SNVs=17) |
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(# total SNVs=1) | (# total SNVs=0) |
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* When you move the cursor on each content, you can see more deailed mutation information on the Tooltip. Those are primary_site,primary_histology,mutation(aa),pubmedID. |
GRCh37 position | Mutation(aa) | Unique sampleID count |
chr16:56388797-56388797 | p.D299D | 3 |
chr16:56388909-56388909 | p.D337H | 3 |
chr16:56388841-56388841 | p.S314L | 2 |
chr16:56370655-56370655 | p.V202V | 2 |
chr16:56385325-56385325 | p.F251F | 2 |
chr16:56370674-56370674 | p.R209C | 2 |
chr16:56362664-56362664 | p.N142S | 2 |
chr16:56370728-56370728 | p.A227T | 2 |
chr16:56362673-56362673 | p.R145Q | 2 |
chr16:56362569-56362569 | p.V111fs*1 | 1 |
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Point Mutation/ Tissue ID | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | 13 | 14 | 15 | 16 | 17 | 18 | 19 | 20 |
# sample | 3 | 3 |   | 11 | 1 |   | 2 |   | 1 |   |   | 9 |   |   | 1 | 1 | 3 | 1 |   | 10 |
# mutation | 3 | 3 |   | 11 | 1 |   | 2 |   | 1 |   |   | 8 |   |   | 1 | 1 | 3 | 1 |   | 11 |
nonsynonymous SNV | 1 | 2 |   | 9 | 1 |   | 2 |   | 1 |   |   | 2 |   |   |   | 1 | 2 |   |   | 7 |
synonymous SNV | 2 | 1 |   | 2 |   |   |   |   |   |   |   | 6 |   |   | 1 |   | 1 | 1 |   | 4 |
cf) Tissue ID; Tissue type (1; BLCA[Bladder Urothelial Carcinoma], 2; BRCA[Breast invasive carcinoma], 3; CESC[Cervical squamous cell carcinoma and endocervical adenocarcinoma], 4; COAD[Colon adenocarcinoma], 5; GBM[Glioblastoma multiforme], 6; Glioma Low Grade, 7; HNSC[Head and Neck squamous cell carcinoma], 8; KICH[Kidney Chromophobe], 9; KIRC[Kidney renal clear cell carcinoma], 10; KIRP[Kidney renal papillary cell carcinoma], 11; LAML[Acute Myeloid Leukemia], 12; LUAD[Lung adenocarcinoma], 13; LUSC[Lung squamous cell carcinoma], 14; OV[Ovarian serous cystadenocarcinoma ], 15; PAAD[Pancreatic adenocarcinoma], 16; PRAD[Prostate adenocarcinoma], 17; SKCM[Skin Cutaneous Melanoma], 18:STAD[Stomach adenocarcinoma], 19:THCA[Thyroid carcinoma], 20:UCEC[Uterine Corpus Endometrial Carcinoma]) |
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* We represented just top 10 SNVs. When you move the cursor on each content, you can see more deailed mutation information on the Tooltip. Those are primary_site, primary_histology, mutation(aa), pubmedID. |
Genomic Position | Mutation(aa) | Unique sampleID count |
chr16:56388797 | p.D337N | 2 |
chr16:56374870 | p.P283Q | 2 |
chr16:56370656 | p.F251F | 2 |
chr16:56388909 | p.G203R,GNAO1 | 2 |
chr16:56385325 | p.D299D | 2 |
chr16:56362673 | p.G92D,GNAO1 | 1 |
chr16:56374784 | p.A227T,GNAO1 | 1 |
chr16:56385394 | p.A301A | 1 |
chr16:56309890 | p.I93I,GNAO1 | 1 |
chr16:56362683 | p.A227A,GNAO1 | 1 |
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* Copy number data were extracted from TCGA using R package TCGA-Assembler. The URLs of all public data files on TCGA DCC data server were gathered on Jan-05-2015. Function ProcessCNAData in TCGA-Assembler package was used to obtain gene-level copy number value which is calculated as the average copy number of the genomic region of a gene. |
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cf) Tissue ID[Tissue type]: BLCA[Bladder Urothelial Carcinoma], BRCA[Breast invasive carcinoma], CESC[Cervical squamous cell carcinoma and endocervical adenocarcinoma], COAD[Colon adenocarcinoma], GBM[Glioblastoma multiforme], Glioma Low Grade, HNSC[Head and Neck squamous cell carcinoma], KICH[Kidney Chromophobe], KIRC[Kidney renal clear cell carcinoma], KIRP[Kidney renal papillary cell carcinoma], LAML[Acute Myeloid Leukemia], LUAD[Lung adenocarcinoma], LUSC[Lung squamous cell carcinoma], OV[Ovarian serous cystadenocarcinoma ], PAAD[Pancreatic adenocarcinoma], PRAD[Prostate adenocarcinoma], SKCM[Skin Cutaneous Melanoma], STAD[Stomach adenocarcinoma], THCA[Thyroid carcinoma], UCEC[Uterine Corpus Endometrial Carcinoma] |
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Gene Expression for GNAO1 |
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* CCLE gene expression data were extracted from CCLE_Expression_Entrez_2012-10-18.res: Gene-centric RMA-normalized mRNA expression data. |
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* Normalized gene expression data of RNASeqV2 was extracted from TCGA using R package TCGA-Assembler. The URLs of all public data files on TCGA DCC data server were gathered at Jan-05-2015. Only eight cancer types have enough normal control samples for differential expression analysis. (t test, adjusted p<0.05 (using Benjamini-Hochberg FDR)) |
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* This plots show the correlation between CNV and gene expression. |
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Gene-Gene Network Information |
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* Co-Expression network figures were drawn using R package igraph. Only the top 20 genes with the highest correlations were shown. Red circle: input gene, orange circle: cell metabolism gene, sky circle: other gene |
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APLP1,BSN,CPLX2,DISP2,DKFZP434H168,AMER3,GNAO1, UNC79,LOC283856,MAPK8IP1,PHF21B,PSD,PTPRN2,RUNDC3A, SNAP25,SPTBN4,SYN1,SYP,SYT4,TMEM145,UNC13A | C11orf94,FOXL2NB,CDSN,COL4A6,CWH43,CYP4F22,FOXD4L6, FOXL2,GNAO1,HS6ST2,KLK2,LOC283856,LPHN3,NETO2, NRK,OR52W1,RAP1GDS1,SCRG1,UPK3A,WIF1,ZNF689 |
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ASB2,CAND2,CLIP3,GNAO1,GPM6A,GRIK5,HSPB8, KIAA2022,LDB3,LMOD1,LONRF2,LRCH2,MAB21L2,MAP6, MYH11,MYLK,MYOCD,PDZRN4,REEP2,SPEG,TCEAL2 | ATP2B4,CACNA1C,CACNA1H,DMD,FRMPD4,GNAO1,GRIK5, ITGA7,KCNB1,KCNMA1,MRVI1,MYH11,TENM3___TENM1,PPP1R12B, PRUNE2,PTGS1,SPEG,SVIL,TACR2,TNS1,TSPAN18 |
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* Co-Expression network figures were drawn using R package igraph. Only the top 20 genes with the highest correlations were shown. Red circle: input gene, orange circle: cell metabolism gene, sky circle: other gene |
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Pharmacological Information for GNAO1 |
There's no related Drug. |
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Cross referenced IDs for GNAO1 |
* We obtained these cross-references from Uniprot database. It covers 150 different DBs, 18 categories. http://www.uniprot.org/help/cross_references_section |
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