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Phenotypic Information (metabolism pathway, cancer, disease, phenome) | |
Gene-Gene Network Information: Co-Expression Network, Interacting Genes & KEGG | |
Gene Summary for PRKACG |
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Phenotypic Information for PRKACG(metabolism pathway, cancer, disease, phenome) |
Cancer Description | |
Cancer | CGAP: PRKACG |
Familial Cancer Database: PRKACG |
* 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/ |
Metabolic Pathway Description | |
REACTOME_INTEGRATION_OF_ENERGY_METABOLISM REACTOME_METABOLISM_OF_LIPIDS_AND_LIPOPROTEINS REACTOME_METABOLISM_OF_CARBOHYDRATES REACTOME_GLUCOSE_METABOLISM |
Others | |
OMIM | 176893; gene. |
Orphanet | |
Disease | KEGG Disease: PRKACG |
MedGen: PRKACG (Human Medical Genetics with Condition) | |
ClinVar: PRKACG | |
Phenotype | MGI: PRKACG (International Mouse Phenotyping Consortium) |
PhenomicDB: PRKACG |
Mutations for PRKACG |
* 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. |
Structural Variants in COSMIC: go to COSMIC mutation histogram |
There's no structural variation information in COSMIC data for this gene. |
Related fusion transcripts : go to Chitars2.0 |
* From mRNA Sanger sequences, Chitars2.0 arranged chimeric transcripts. This table shows PRKACG 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 |
Other DBs for Structural Variants |
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Copy Number Variations in COSMIC: go to COSMIC mutation CNV/Expr |
There's no copy number variation information in COSMIC data for this gene. |
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SNV Counts per Each Loci in COSMIC data: go to COSMIC point mutation |
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Somatic Mutation Counts per Tissue in COSMIC data |
Stat. for Non-Synonymous SNVs (# total SNVs=48) | (# total SNVs=20) |
(# total SNVs=1) | (# total SNVs=0) |
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Top 10 SNVs Having the Most Samples in COSMIC data |
* 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 |
chr9:71628115-71628115 | p.F298F | 4 |
chr9:71628097-71628097 | p.I304I | 3 |
chr9:71628435-71628435 | p.V192M | 3 |
chr9:71628114-71628114 | p.A299T | 3 |
chr9:71628877-71628877 | p.F44F | 3 |
chr9:71628152-71628152 | p.R286K | 3 |
chr9:71628289-71628289 | p.Y240Y | 2 |
chr9:71628484-71628484 | p.I175I | 2 |
chr9:71628589-71628589 | p.S140R | 2 |
chr9:71628409-71628409 | p.C200C | 2 |
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SNV Counts per Each Loci in TCGA data |
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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 | 1 | 3 |   | 11 |   |   | 3 |   | 2 |   |   | 2 | 1 | 1 |   | 1 | 17 | 7 |   | 12 |
# mutation | 1 | 3 |   | 10 |   |   | 3 |   | 2 |   |   | 2 | 1 | 1 |   | 1 | 19 | 8 |   | 12 |
nonsynonymous SNV |   | 1 |   | 6 |   |   | 1 |   | 2 |   |   | 2 | 1 | 1 |   |   | 8 | 5 |   | 8 |
synonymous SNV | 1 | 2 |   | 4 |   |   | 2 |   |   |   |   |   |   |   |   | 1 | 11 | 3 |   | 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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Top 10 SNVs Having the Most Samples in TCGA data |
* 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 |
chr9:71628877 | p.F44F | 3 |
chr9:71628097 | p.I304I | 3 |
chr9:71628114 | p.C200C | 2 |
chr9:71628484 | p.A299T | 2 |
chr9:71628130 | p.K293K | 2 |
chr9:71628979 | p.V192M | 2 |
chr9:71628021 | p.I175I | 2 |
chr9:71628409 | p.R48K | 2 |
chr9:71628435 | p.D330N | 2 |
chr9:71628059 | p.P317L | 2 |
Other DBs for Point Mutations |
Copy Number for PRKACG in TCGA |
* 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. |
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 PRKACG |
Gene Expression in Cancer Cell-lines (CCLE) |
* CCLE gene expression data were extracted from CCLE_Expression_Entrez_2012-10-18.res: Gene-centric RMA-normalized mRNA expression data. |
Differential Gene Expression in Primary Tumors (TCGA) |
* 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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CNV vs Gene Expression Plot |
* This plots show the correlation between CNV and gene expression. |
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Gene-Gene Network Information |
Co-Expressed gene's network Plot |
* 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 |
CLRN2,KRTAP19-2,KRTAP25-1,KRTAP6-1,MUC17,OPRM1,OR11A1, OR13F1,OR4C16,OR4L1,OR5AP2,OR5D18,OR5L2,OR6C65, OR6C75,OR8H3,POM121L12,PRKACG,REG1P,TAAR2,TAAR5 | SLC35G3,AMZ2P1,CCDC70,CSNK1A1P1,DPPA2,ELMOD1,GLT6D1, KRTAP9-4,LILRP2,OR10G3,OR2T2,OR4A5,OR5F1,OR7G3, OR8H2,PRB1,PRKACG,RAB9BP1,SNORA32,SNORA71C,SVOP | ||||
BMPER,NAT16,CCDC144NL,CTAG1B,CTXN3,DYNLL2,KCNIP4, KRTAP10-10,KRTAP10-5,LOC389493,LOC572558,OR51B4,OR52D1,POTEH, PRKACG,SLC10A4,SLC6A11,TMEM213,UBE2U,WDR87,ZNF492 | SLC35G3,BEND2,LINC00305,SSMEM1,CD300LD,FAM74A4,GAGE10, LRIT1,MSX2P1,NXF4,OR52E6,PAPOLB,PLCZ1,PRKACG, SCARNA16,SLC22A24,SLC9C2,SPRR2G,STRA8,TRIM24,UBASH3B, ZN |
Co-Expressed gene's Protein-protein interaction Network Plot |
* 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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Interacting Genes (from Pathway Commons) |
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Pharmacological Information for PRKACG |
Cross-referenced pharmacological DB IDs from Uniprot |
DB Category | DB Name | DB's ID and Url link |
Chemistry | ChEMBL | CHEMBL2094138; -. |
Chemistry | GuidetoPHARMACOLOGY | 1478; -. |
Organism-specific databases | PharmGKB | PA33750; -. |
Organism-specific databases | CTD | 5568; -. |
Drug-Gene Interaction Network |
* Gene Centered Interaction Network. |
* Drug Centered Interaction Network. |
DrugBank ID | Target Name | Drug Groups | Generic Name | Drug Centered Network | Drug Structure |
DB00125 | protein kinase, cAMP-dependent, catalytic, gamma | approved; nutraceutical | L-Arginine | ||
DB00155 | protein kinase, cAMP-dependent, catalytic, gamma | approved; nutraceutical | L-Citrulline | ||
DB00435 | protein kinase, cAMP-dependent, catalytic, gamma | approved | Nitric Oxide | ||
DB00988 | protein kinase, cAMP-dependent, catalytic, gamma | approved | Dopamine | ||
DB00171 | protein kinase, cAMP-dependent, catalytic, gamma | approved; nutraceutical | Adenosine triphosphate | ||
DB00770 | protein kinase, cAMP-dependent, catalytic, gamma | approved; investigational | Alprostadil | ||
DB00668 | protein kinase, cAMP-dependent, catalytic, gamma | approved | Epinephrine | ||
DB00131 | protein kinase, cAMP-dependent, catalytic, gamma | approved; nutraceutical | Adenosine monophosphate | ||
DB00396 | protein kinase, cAMP-dependent, catalytic, gamma | approved | Progesterone | ||
DB00938 | protein kinase, cAMP-dependent, catalytic, gamma | approved | Salmeterol |
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Cross referenced IDs for PRKACG |
* 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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