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| TissGeneSummary for FAM227B |
Gene summary |
| Basic gene information | Gene symbol | FAM227B |
| Gene name | family with sequence similarity 227, member B | |
| Synonyms | C15orf33 | |
| Cytomap | UCSC genome browser: 15q21.2 | |
| Type of gene | protein-coding | |
| RefGenes | NM_152647.2, | |
| Description | protein FAM227B | |
| Modification date | 20141207 | |
| dbXrefs | HGNC : HGNC | |
| Ensembl : ENSG00000166262 | ||
| HPRD : 08139 | ||
| Vega : OTTHUMG00000172328 | ||
| Protein | UniProt: go to UniProt's Cross Reference DB Table | |
| Expression | CleanEX: HS_FAM227B | |
| BioGPS: 196951 | ||
| Pathway | NCI Pathway Interaction Database: FAM227B | |
| KEGG: FAM227B | ||
| REACTOME: FAM227B | ||
| Pathway Commons: FAM227B | ||
| Context | iHOP: FAM227B | |
| ligand binding site mutation search in PubMed: FAM227B | ||
| UCL Cancer Institute: FAM227B | ||
| Assigned class in TissGDB* | C | |
| Included tissue-specific gene expression resources | TiGER,GTEx | |
| Specific-tissues in normal samples (assigned by TissGDB using HPA, TiGER, and GTEx) | Soft tissueTestis | |
| Cancer types related to the specific-tissues in cancer samples (assigned by TissGDB using TCGA) | SARCTGCT | |
| Reference showing the relevant tissue of FAM227B | ||
| Description by TissGene annotations | ||
| * Class A consists of genes with literature evidence and is part of the cTissGenes. Class B consists of only cTissGenes without additional evidence. The remaining genes belong to Class C. |
Gene ontology having evidence of Inferred from Direct Assay (IDA) from Entrez |
| GO ID | GO term | PubMed ID |
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| TissGeneExp for FAM227B |
Gene expressions across 28 cancer types (X-axis: cancer type and Y-axis: log2(norm_counts+1))(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16) |
Gene isoform expressions across 28 cancer types (X-axis: cancer type and Y-axis: log2(norm_counts+1))(TCGA pan-cancer tcga_rsem_isoform_tpm, version 2016-09-01) |
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Gene expressions across normal tissues of GTEx data(GTEx GTEx_Analysis_v6_RNA-seq_RNA-SeQCv1.1.8_gene_rpkm.gct) - Here, we shows the matched tissue types only among our 28 cancer types. |
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Different expressions across 14 cancer types with more than 10 samples between matched tumors and normals (X-axis: cancer type and Y-axis: log2(norm_counts+1))(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16) |
| - Significantly differentially expressed cancer types and information. (|Fold change|>1 and FDR<0.05) |
| Cancer type | Mean(exp) in tumor | Mean(exp) in matched normal | Log2FC | P-val. | FDR |
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| TissGene-miRNA for FAM227B |
Significantly anti-correlated miRNAs of TissGene across 28 cancer types(Gene-miRNA relations from TargetScanHuman Relsease 7.1, Conserved_Site_Context_Scores.txt.zip, 06.01.2016) (TCGA IlluminaHiSeq_miRNASeq, log2(RPM+1) data, version 2016-11-21) (TCGA IlluminaHiSeq_RNASeqV2, log2(normalized_count+1) data, version 2016-08-16) (Spearman’s Rank Correlation (p-value<0.05 and coefficient<-0.25)) |
| Cancer type | miRNA id | miRNA accession | P-val. | Coeff. | # samples |
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| TissGeneMut for FAM227B |
| TissGeneSNV for FAM227B |
nsSNV counts per each loci.Different colors of circles represent different cancer types. Circle size denotes number of samples. (TCGA somatic mutation (SNPs and small INDELs) data, version 2016-04-25) * Click on the image to enlarge it in a new window. |
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Somatic nucleotide variants of TissGene across 28 cancer types (X-axis: cancer type and Y-axis: % of mutated samples) The numbers in parentheses are numbers of samples with mutation (nsSNVs). (TCGA somatic mutation (SNPs and small INDELs) data, version 2016-04-25) |
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| - nsSNVs sorted by frequency. |
| AAchange | Cancer type | # samples |
| p.D276N | SKCM | 2 |
| p.Q422R | LUAD | 1 |
| p.S309F | LUAD | 1 |
| p.H179R | HNSC | 1 |
| p.G298S | HNSC | 1 |
| p.G389S | SKCM | 1 |
| p.R218K | SKCM | 1 |
| p.E158K | SKCM | 1 |
| p.E72K | SKCM | 1 |
| p.I171M | PAAD | 1 |
| p.P75S | SKCM | 1 |
| p.D340N | STAD | 1 |
| p.Y396C | LIHC | 1 |
| p.D330H | LUAD | 1 |
| p.Q20X | STAD | 1 |
| p.Q20H | LUAD | 1 |
| p.P268S | SKCM | 1 |
| p.A437E | THYM | 1 |
| p.I57V | HNSC | 1 |
| p.E265* | HNSC | 1 |
| p.R184S | LIHC | 1 |
| p.R9S | HNSC | 1 |
| p.E111Q | BLCA | 1 |
| p.A200T | PAAD | 1 |
| p.R327K | SKCM | 1 |
| p.T262A | STAD | 1 |
| p.S358F | SKCM | 1 |
| p.Q296R | LUAD | 1 |
| p.S150I | HNSC | 1 |
| p.P350T | HNSC | 1 |
| p.H471Y | STAD | 1 |
| p.S100P | BLCA | 1 |
| p.P16H | STAD | 1 |
| p.T418I | BLCA | 1 |
| p.G283R | SKCM | 1 |
| p.R243* | SKCM | 1 |
| p.A368V | STAD | 1 |
| p.K144N | STAD | 1 |
| p.E219K | SKCM | 1 |
| p.G283E | SARC | 1 |
| p.T234A | SKCM | 1 |
| p.R120Q | SKCM | 1 |
| p.G298V | PRAD | 1 |
| p.E27* | LUAD | 1 |
| p.S336L | SKCM | 1 |
| p.F236L | SKCM | 1 |
| p.D36N | SKCM | 1 |
| p.M84I | LUAD | 1 |
| p.A258D | SARC | 1 |
| p.S271N | LUAD | 1 |
| p.T53P | LUAD | 1 |
| p.R184K | HNSC | 1 |
| p.L211F | SKCM | 1 |
| p.C52W | CESC | 1 |
| p.R243X | SKCM | 1 |
| p.L162Q | KIRC | 1 |
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| TissGeneCNV for FAM227B |
Copy number variations of TissGene across 28 cancer types (X-axis: cancer type and Y-axis: % of CNV samples)(TCGA Gistic2_CopyNumber_Gistic2_all_data_by_genes, Gistic2 copy number data, version 2016-08-16) |
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| TissGeneFusions for FAM227B |
Fusion genes including TissGene (ChimerDB 3.0, 2016-12-01 and TCGA fusion Portal 2015-12-01) |
| Database | Src | Cancer type | Sample | Fusion gene | ORF | 5'-gene BP | 3'-gene BP |
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| TissGeneNet for FAM227B |
Co-expressed gene networks based on protein-protein interaction data (CePIN)(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16) (PINA2 ppi data) |
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| TissGeneProg for FAM227B |
Kaplan-Meier plots with logrank tests of overall survival (OS) using 28 cancer types (TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16) (TCGA clinicalMatrix, phenotype data, version 2016-04-27) * Click on the image to enlarge it in a new window. |
Kaplan-Meier plots with logrank test of relapse free survival (RFS) using 28 cancer types (TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16) (TCGA clinicalMatrix, phenotype data, version 2016-04-27) * Click on the image enlarge it in a new window. |
Forest plot of Cox proportional hazard ratio (HR) and 95% CI of overall survival (OS) using 28 cancer types (TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16) (TCGA clinicalMatrix, phenotype data, version 2016-04-27) * Click on the image enlarge it in a new window. |
Forest plot of Cox proportional hazard ratio (HR) and 95% CI of relapse free survival (RFS) using 28 cancer types (TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16) (TCGA clinicalMatrix, phenotype data, version 2016-04-27) * Click on the image enlarge it in a new window. |
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| TissGeneClin for FAM227B |
| TissGeneDrug for FAM227B |
Drug information targeting TissGene (DrugBank Version 5.0.6, 2017-04-01) |
| DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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| TissGeneDisease for FAM227B |
Disease information associated with TissGene (DisGeNet, 2016-06-01) |
| Disease ID | Disease name | # pubmeds | Source |
| umls:C0018021 | Goiter | 1 | GAD |
| umls:C0040336 | Tobacco Use Disorder | 1 | GAD |