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Phenotypic Information (metabolism pathway, cancer, disease, phenome) | |
Gene-Gene Network Information: Co-Expression Network, Interacting Genes & KEGG | |
Gene Summary for FABP6 |
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Phenotypic Information for FABP6(metabolism pathway, cancer, disease, phenome) |
Cancer Description | |
Cancer | CGAP: FABP6 |
Familial Cancer Database: FABP6 |
* 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_LIPIDS_AND_LIPOPROTEINS |
Others | |
OMIM | |
Orphanet | |
Disease | KEGG Disease: FABP6 |
MedGen: FABP6 (Human Medical Genetics with Condition) | |
ClinVar: FABP6 | |
Phenotype | MGI: FABP6 (International Mouse Phenotyping Consortium) |
PhenomicDB: FABP6 |
Mutations for FABP6 |
* 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 FABP6 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 |
DB067617 | FABP6 | 1 | 357 | 5 | 159624751 | 159640827 | CRK | 355 | 507 | 17 | 1340299 | 1340451 |
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 |   |   |   |   |   |   |   |   |   |   |   |   |   |   |   |   | |||
GAIN (# sample) |   |   |   |   |   |   |   |   |   |   |   |   |   |   |   |   |   | |||
LOSS (# sample) | 2 |   |   |   |   |   |   |   |   |   |   |   |   |   |   |   |   |
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=16) | (# total SNVs=6) |
(# 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 |
chr5:159656585-159656585 | p.F7L | 3 |
chr5:159659148-159659148 | p.I37I | 3 |
chr5:159661892-159661892 | p.E103D | 2 |
chr5:159659203-159659203 | p.G56W | 2 |
chr5:159656578-159656578 | p.G5D | 2 |
chr5:159661872-159661872 | p.N97Y | 2 |
chr5:159659202-159659202 | p.S55S | 1 |
chr5:159661895-159661895 | p.I104I | 1 |
chr5:159659229-159659229 | p.F64F | 1 |
chr5:159665643-159665643 | p.R122S | 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 |   | 1 |   | 4 | 1 |   | 1 |   | 1 |   |   | 2 | 2 |   |   |   | 3 | 4 |   | 3 |
# mutation |   | 1 |   | 4 | 1 |   | 1 |   | 1 |   |   | 2 | 2 |   |   |   | 3 | 4 |   | 3 |
nonsynonymous SNV |   | 1 |   | 2 | 1 |   | 1 |   | 1 |   |   | 1 | 1 |   |   |   |   | 3 |   | 2 |
synonymous SNV |   |   |   | 2 |   |   |   |   |   |   |   | 1 | 1 |   |   |   | 3 | 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 |
chr5:159656578 | p.E103E,FABP6 | 2 |
chr5:159661892 | p.G5D,FABP6 | 2 |
chr5:159659125 | p.S51Y,FABP6 | 1 |
chr5:159665630 | p.G56R,FABP6 | 1 |
chr5:159659135 | p.F64F,FABP6 | 1 |
chr5:159659148 | p.K68E,FABP6 | 1 |
chr5:159640748 | p.G89G,FABP6 | 1 |
chr5:159659189 | p.F95F,FABP6 | 1 |
chr5:159640768 | p.L19L,FABP6 | 1 |
chr5:159659203 | p.C26Y,FABP6 | 1 |
Other DBs for Point Mutations |
Copy Number for FABP6 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 FABP6 |
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 |
AADAT,ABCC12,ACE2,ANKRD26P1,C2orf83,CELP,CKMT2, CSAG1,CSTB,FABP6,GGT1,GGTLC1,GGTLC2,H2AFB1, H2BFWT,LCN15,LYZL4,PLA2G4E,SLED1,SSX4,SSX6 | ADH7,CLPSL2,CALML3,DLX1,DNAJB3,ETNK2,FABP6, FAM81B,HMGB4,KRT13,KRTAP15-1,LOC286359,MRFAP1,OR10G8, OR4P4,PNMT,PTHLH,SLC18A3,SLC39A11,TNFSF11,TSPAN1 | ||||
C12orf45,MAPKAPK5-AS1,C12orf73,SWSAP1,SMIM15,CCNH,FABP6, MED7,METTL5,MFF,MTERF2,NACA,NDUFAF2,PDCD5, POC5,QTRT1,TAF7,TBCA,TTC1,ZNF443,ZNF799 | AADAC,APOA1,APOA4,APOC3,C17orf78,CRISP1,FABP6, FAM99A,FAM99B,GSTA5,KCNJ13,LCE3E,LOC388428,MOS, ONECUT3,OR10H1,OR10H5,OR4N5,PWAR4___F2RL3___PAWR,SLC2A2,SPANXN3 |
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 FABP6 |
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 |
DB02659 | fatty acid binding protein 6, ileal | experimental | Cholic Acid | ||
DB02691 | fatty acid binding protein 6, ileal | experimental | N-Cholylglycine | ||
DB04348 | fatty acid binding protein 6, ileal | experimental | Taurocholic Acid | ||
DB00145 | fatty acid binding protein 6, ileal | approved; nutraceutical | Glycine |
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Cross referenced IDs for FABP6 |
* 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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