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Phenotypic Information (metabolism pathway, cancer, disease, phenome) | |
Gene-Gene Network Information: Co-Expression Network, Interacting Genes & KEGG | |
Gene Summary for ALOX15 |
Basic gene info. | Gene symbol | ALOX15 |
Gene name | arachidonate 15-lipoxygenase | |
Synonyms | 12-LOX|15-LOX-1|15LOX-1 | |
Cytomap | UCSC genome browser: 17p13.3 | |
Genomic location | chr17 :4534213-4544960 | |
Type of gene | protein-coding | |
RefGenes | NM_001140.3, | |
Ensembl id | ENSG00000161905 | |
Description | 12/15-lipoxygenase15-LOX15-lipooxygenase-1arachidonate 12-lipoxygenase, leukocyte-typearachidonate omega-6 lipoxygenase | |
Modification date | 20141222 | |
dbXrefs | MIM : 152392 | |
HGNC : HGNC | ||
Ensembl : ENSG00000161905 | ||
HPRD : 01067 | ||
Vega : OTTHUMG00000090746 | ||
Protein | UniProt: P16050 go to UniProt's Cross Reference DB Table | |
Expression | CleanEX: HS_ALOX15 | |
BioGPS: 246 | ||
Gene Expression Atlas: ENSG00000161905 | ||
The Human Protein Atlas: ENSG00000161905 | ||
Pathway | NCI Pathway Interaction Database: ALOX15 | |
KEGG: ALOX15 | ||
REACTOME: ALOX15 | ||
ConsensusPathDB | ||
Pathway Commons: ALOX15 | ||
Metabolism | MetaCyc: ALOX15 | |
HUMANCyc: ALOX15 | ||
Regulation | Ensembl's Regulation: ENSG00000161905 | |
miRBase: chr17 :4,534,213-4,544,960 | ||
TargetScan: NM_001140 | ||
cisRED: ENSG00000161905 | ||
Context | iHOP: ALOX15 | |
cancer metabolism search in PubMed: ALOX15 | ||
UCL Cancer Institute: ALOX15 | ||
Assigned class in ccmGDB | A - This gene has a literature evidence and it belongs to cancer gene. | |
References showing role of ALOX15 in cancer cell metabolism | 1. Hu Y, Sun H, O'Flaherty JT, Edwards IJ (2013) 15-Lipoxygenase-1-mediated metabolism of docosahexaenoic acid is required for syndecan-1 signaling and apoptosis in prostate cancer cells. Carcinogenesis 34: 176-182. doi: 10.1093/carcin/bgs324. pmid: 3584949. go to article 2. Suraneni MV, Moore JR, Zhang D, Badeaux M, Macaluso MD, et al. (2014) Tumor-suppressive functions of 15-Lipoxygenase-2 and RB1CC1 in prostate cancer. Cell Cycle 13: 1798-1810. doi: 10.4161/cc.28757. pmid: 4111726. go to article 3. Guo Y, Nie D (2014) Tumor-suppressing 15-lipoxygenase-2: time for prime time? Cell Cycle 13: 1836-1837. doi: 10.4161/cc.29328. pmid: 4111746. go to article |
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Phenotypic Information for ALOX15(metabolism pathway, cancer, disease, phenome) |
Cancer Description | |
Cancer | CGAP: ALOX15 |
Familial Cancer Database: ALOX15 |
* 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 | |
KEGG_ARACHIDONIC_ACID_METABOLISM KEGG_LINOLEIC_ACID_METABOLISM |
Others | |
OMIM | 152392; gene. |
Orphanet | |
Disease | KEGG Disease: ALOX15 |
MedGen: ALOX15 (Human Medical Genetics with Condition) | |
ClinVar: ALOX15 | |
Phenotype | MGI: ALOX15 (International Mouse Phenotyping Consortium) |
PhenomicDB: ALOX15 |
Mutations for ALOX15 |
* 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 ALOX15 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=41) | (# total SNVs=11) |
(# 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 |
chr17:4542791-4542791 | p.E91K | 3 |
chr17:4540538-4540538 | p.E275K | 2 |
chr17:4542894-4542894 | p.Y56Y | 2 |
chr17:4536722-4536722 | p.G412E | 2 |
chr17:4542381-4542381 | p.R128R | 2 |
chr17:4541560-4541560 | p.F253F | 2 |
chr17:4536769-4536769 | p.T396T | 2 |
chr17:4541604-4541604 | p.V239M | 2 |
chr17:4536197-4536197 | p.R500Q | 2 |
chr17:4540413-4540413 | p.I316M | 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 | 2 |   | 6 | 1 |   | 3 |   |   |   |   | 4 | 3 | 2 |   | 1 | 11 | 3 |   | 8 |
# mutation | 1 | 2 |   | 7 | 1 |   | 3 |   |   |   |   | 4 | 3 | 2 |   | 1 | 11 | 3 |   | 8 |
nonsynonymous SNV | 1 | 2 |   | 2 |   |   | 1 |   |   |   |   | 4 | 3 | 2 |   | 1 | 6 | 3 |   | 8 |
synonymous SNV |   |   |   | 5 | 1 |   | 2 |   |   |   |   |   |   |   |   |   | 5 |   |   |   |
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 |
chr17:4540413 | p.T396T | 2 |
chr17:4540538 | p.I316M | 2 |
chr17:4536769 | p.E275K | 2 |
chr17:4536516 | p.R599H | 1 |
chr17:4535217 | p.G406E | 1 |
chr17:4542248 | p.A186T | 1 |
chr17:4536586 | p.I592I | 1 |
chr17:4540418 | p.G147W | 1 |
chr17:4535233 | p.S587C | 1 |
chr17:4542357 | p.P380L | 1 |
Other DBs for Point Mutations |
Copy Number for ALOX15 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 ALOX15 |
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 |
ACADL,ALOX15B,APOD,C15orf43,CLDN8,FKBP5,GGT1, GGT3P,HAAO,LST-3TM12,MPV17L,MVK,OXER1,PNLIPRP3, RLN3,SERHL2,SERHL,SLCO1B1,SPINK8,SULT1C3,UGT2B28 | ABCC11,ACSL3,ADAM2,ALOX15B,APOD,B3GAT1,C15orf43, DHRS2,DMRTC2,GGT1,HPGD,IDI1,LST-3TM12,MPV17L, PNLIPRP3,SERHL2,SERHL,SRD5A1,TARP,TMPRSS11F,UGT2B10 |
ALOX15B,CRISP2,EPYC,FGL1,FOLH1,FOXE1,GABBR2, GPR37L1,GSTTP1,GSTTP2,HIST1H4A,HSPA2,HTR1B,ITLN1, ITLN2,LOC29034,LYZL6,GRIK1-AS1,SHISA3,UGT2B4,UMOD | ALOX15B,ANTXRL,C15orf43,CA5A,PTGDR2,HIST1H1A,ITGA10, KCNS2,LOC731789,LY6K,MC3R,MERTK,MYH13,OR10J3, OR1L6,PSCA,SDHAP2,SIGLEC8,SNORA71D,SP9,TRPC3 |
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 ALOX15 |
There's no related Drug. |
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Cross referenced IDs for ALOX15 |
* 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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