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Phenotypic Information (metabolism pathway, cancer, disease, phenome) | |
Gene-Gene Network Information: Co-Expression Network, Interacting Genes & KEGG | |
Gene Summary for NFS1 |
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Phenotypic Information for NFS1(metabolism pathway, cancer, disease, phenome) |
Cancer Description | |
Cancer | CGAP: NFS1 |
Familial Cancer Database: NFS1 |
* This gene is included in those cancer gene databases. |
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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_METABOLISM_OF_VITAMINS_AND_COFACTORS |
Others | |
OMIM | |
Orphanet | |
Disease | KEGG Disease: NFS1 |
MedGen: NFS1 (Human Medical Genetics with Condition) | |
ClinVar: NFS1 | |
Phenotype | MGI: NFS1 (International Mouse Phenotyping Consortium) |
PhenomicDB: NFS1 |
Mutations for NFS1 |
* 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 |
- Statistics for Tissue and Mutation type | Top |
- For Inter-chromosomal Variations |
* Inter-chromosomal variantions includes 'interchromosomal amplicon to amplicon', 'interchromosomal amplicon to non-amplified dna', 'interchromosomal insertion', 'Interchromosomal unknown type'. |
- 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'. |
Sample | Symbol_a | Chr_a | Start_a | End_a | Symbol_b | Chr_b | Start_b | End_b |
haematopoietic_and_lymphoid_tissue | NFS1 | chr20 | 34265764 | 34265764 | NFS1 | chr20 | 34265764 | 34265764 |
ovary | NFS1 | chr20 | 34256829 | 34256849 | chr1 | 26967961 | 26967981 |
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) |
Related fusion transcripts : go to Chitars2.0 |
* From mRNA Sanger sequences, Chitars2.0 arranged chimeric transcripts. This table shows NFS1 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 |
DW417230 | NFS1 | 17 | 107 | 20 | 34276829 | 34276919 | HGD | 106 | 134 | 3 | 120389826 | 120389861 |
Other DBs for Structural Variants |
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Copy Number Variations in COSMIC: go to COSMIC mutation CNV/Expr |
Mutation type/ Tissue ID | brca | cns | cerv | endome | haematopo | kidn | Lintest | liver | lung | ns | ovary | pancre | prost | skin | stoma | thyro | urina | |||
Total # sample | 2 |   |   |   |   |   | 1 |   | 1 |   |   |   |   |   |   |   |   | |||
GAIN (# sample) | 2 |   |   |   |   |   | 1 |   | 1 |   |   |   |   |   |   |   |   | |||
LOSS (# sample) |   |   |   |   |   |   |   |   |   |   |   |   |   |   |   |   |   |
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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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=33) | (# total SNVs=7) |
(# total SNVs=0) | (# 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 |
chr20:34262318-34262318 | p.E364K | 2 |
chr20:34263099-34263099 | p.R272R | 2 |
chr20:34260686-34260686 | p.R434Q | 2 |
chr20:34268745-34268745 | p.Q235R | 1 |
chr20:34261595-34261595 | p.S383C | 1 |
chr20:34278462-34278462 | p.R145L | 1 |
chr20:34263027-34263027 | p.V296V | 1 |
chr20:34285711-34285711 | p.V73V | 1 |
chr20:34268746-34268746 | p.Q235* | 1 |
chr20:34262295-34262295 | p.K371K | 1 |
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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 | 2 | 2 | 1 | 6 |   |   | 1 |   | 4 |   |   | 6 | 3 |   |   |   | 4 | 2 |   | 4 |
# mutation | 2 | 2 | 1 | 6 |   |   | 1 |   | 4 |   |   | 6 | 3 |   |   |   | 4 | 2 |   | 6 |
nonsynonymous SNV | 2 | 1 |   | 6 |   |   | 1 |   | 3 |   |   | 5 | 3 |   |   |   | 2 | 1 |   | 5 |
synonymous SNV |   | 1 | 1 |   |   |   |   |   | 1 |   |   | 1 |   |   |   |   | 2 | 1 |   | 1 |
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 |
chr20:34284379 | p.I271I,NFS1 | 1 |
chr20:34262500 | p.S181I | 1 |
chr20:34268659 | p.R270Q,NFS1 | 1 |
chr20:34285610 | p.P177Q | 1 |
chr20:34262504 | p.E265G,NFS1 | 1 |
chr20:34268744 | p.I135T,NFS1 | 1 |
chr20:34257603 | p.V245V,NFS1 | 1 |
chr20:34285617 | p.V110L,NFS1 | 1 |
chr20:34262522 | p.Q231H,NFS1 | 1 |
chr20:34268745 | p.R107H,NFS1 | 1 |
Other DBs for Point Mutations |
Copy Number for NFS1 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 NFS1 |
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 |
C20orf24,AAR2,CEP250,CPNE1,DSN1,DYNLRB1,EDEM2, EIF6,ERGIC3,GSS,LOC647979,MOCS3,NCOA6,NDRG3, NFS1,PHF20,PIGU,RBM39,ROMO1,TRPC4AP,UQCC1 | ATP5A1,C21orf33,CLYBL,COQ6,CPT2,CYC1,DNAJA3, ERAL1,HAX1,HSPA9,IDH3B,MRPL37,MRPL44,MRPS18B, MRPS7,NDUFA10,NFS1,SNRNP25,TACO1,TSFM,TXN2 | ||||
ACTR5,AAR2,CDK5RAP1,CPNE1,CTNNBL1,DDX27,DHX35, EIF2S2,EIF6,GSS,MTG2,TTI1,NFS1,PIGU, POFUT1,RALY,NELFCD,TM9SF4,TRPC4AP,UBE2V1,UQCC1 | ADH1C,ADH6,DDAH1,EHHADH,FAM117B,HMGCS2,HOXB6, HOXB8,KIFAP3,LRPPRC,NAALADL2,NDUFA10,NFS1,PAQR5, PCCA,SATL1,SH2D4A,SIRT5,SLC19A1,SLC38A4,SUCLG2 |
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 NFS1 |
Cross-referenced pharmacological DB IDs from Uniprot |
DB Category | DB Name | DB's ID and Url link |
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 |
DB00114 | NFS1 nitrogen fixation 1 homolog (S. cerevisiae) | nutraceutical | Pyridoxal Phosphate | ||
DB00151 | NFS1 nitrogen fixation 1 homolog (S. cerevisiae) | approved; nutraceutical | L-Cysteine | ||
DB00160 | NFS1 nitrogen fixation 1 homolog (S. cerevisiae) | approved; nutraceutical | L-Alanine |
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Cross referenced IDs for NFS1 |
* 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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