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Phenotypic Information (metabolism pathway, cancer, disease, phenome) | |
Gene-Gene Network Information: Co-Expression Network, Interacting Genes & KEGG | |
Gene Summary for SLC44A4 |
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Phenotypic Information for SLC44A4(metabolism pathway, cancer, disease, phenome) |
Cancer Description | |
Cancer | CGAP: SLC44A4 |
Familial Cancer Database: SLC44A4 |
* 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_PHOSPHOLIPID_METABOLISM REACTOME_METABOLISM_OF_LIPIDS_AND_LIPOPROTEINS |
Mutations for SLC44A4 |
* 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 SLC44A4 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 |
BI026665 | MYH9 | 2 | 140 | 22 | 36727986 | 36728125 | SLC44A4 | 129 | 281 | 6 | 3171348 | 3171501 | |
BF509779 | SLC44A4 | 141 | 313 | 6 | 3164418 | 3164590 | SLC44A4 | 307 | 409 | 6 | 3164214 | 3164316 | |
BC014659 | SLC44A4 | 92 | 2565 | 6 | 3163722 | 3176652 | ANKRD17 | 2562 | 2583 | 4 | 74084357 | 74084378 |
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=39) | (# total SNVs=16) |
(# total SNVs=3) | (# total SNVs=7) |
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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 |
chr6:31842534-31842535 | p.N144fs*55 | 3 |
chr6:31833864-31833864 | p.V425L | 2 |
chr6:31838832-31838832 | p.? | 2 |
chr6:31838468-31838468 | p.A317T | 2 |
chr6:31842535-31842536 | p.N144fs*55 | 2 |
chr6:31836957-31836957 | p.P403L | 2 |
chr6:31846741-31846741 | p.R6L | 2 |
chr6:31833482-31833482 | p.D523H | 2 |
chr6:31833747-31833747 | p.V464I | 2 |
chr6:31833528-31833528 | p.L507L | 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 | 4 | 1 | 1 | 9 | 1 |   | 2 |   | 2 |   |   | 7 | 4 | 3 |   |   | 9 | 9 |   | 7 |
# mutation | 4 | 1 | 1 | 8 | 1 |   | 2 |   | 2 |   |   | 7 | 4 | 3 |   |   | 9 | 9 |   | 7 |
nonsynonymous SNV | 2 | 1 | 1 | 5 | 1 |   |   |   | 2 |   |   | 3 | 2 | 3 |   |   | 7 | 8 |   | 5 |
synonymous SNV | 2 |   |   | 3 |   |   | 2 |   |   |   |   | 4 | 2 |   |   |   | 2 | 1 |   | 2 |
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 |
chr6:31838664 | p.A246T,SLC44A4 | 2 |
chr6:31832449 | p.D622G,SLC44A4 | 2 |
chr6:31833833 | p.V17V,SLC44A4 | 1 |
chr6:31832450 | p.G605V,SLC44A4 | 1 |
chr6:31838621 | p.F443S,SLC44A4 | 1 |
chr6:31842560 | p.R242Q,SLC44A4 | 1 |
chr6:31833349 | p.Y13C,SLC44A4 | 1 |
chr6:31833838 | p.D586N,SLC44A4 | 1 |
chr6:31832499 | p.P437P,SLC44A4 | 1 |
chr6:31838641 | p.Y233C,SLC44A4 | 1 |
Other DBs for Point Mutations |
Copy Number for SLC44A4 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 SLC44A4 |
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 |
ARFIP2,CCDC176,C9orf152,CCDC125,CCDC160,CD46,CREB3L1, CREB3L4,ERBB3,ERGIC1,FOXA1,GALNT6,GALNT7,GPR160, MIA3,MLPH,MUC1,SEC16A,SLC44A4,SPDEF,ZBTB42 | C3orf52,CANT1,CLDN7,DLG3,GALNT6,GOLM1,HN1L, LEO1,LRRC46,MAGED2,MAPK13,MLPH,MUC1,PRR15, PRR15L,SEC14L2,SEZ6L2,SLC35A2,SLC44A4,SLC9A3R1,XBP1 |
BCAS1,C1orf106,C4orf19,CAPN5,CASP7,CDHR5,DNM2, FA2H,GPA33,HECTD3,ITM2C,MGLL,MUC13,NR3C2, PLS1,PTPRH,SLC44A4,STYK1,TJP3,TMEM63B,TSPAN1 | CAPN2,CAPN5,CDCP1,CLCN2,CNNM4,GBA,ITM2C, MARK2,OSBPL2,PAK1,PCDH1,PCSK7,PRSS8,RAB19, SCAMP2,SCNN1A,SGPP2,SLC44A4,ST14,TJP3,TMEM63B |
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 SLC44A4 |
There's no related Drug. |
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Cross referenced IDs for SLC44A4 |
* 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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