TissGeneSummary for GAN |
Gene summary |
Basic gene information | Gene symbol | GAN |
Gene name | gigaxonin | |
Synonyms | GAN1|KLHL16 | |
Cytomap | UCSC genome browser: 16q24.1 | |
Type of gene | protein-coding | |
RefGenes | NM_022041.3, | |
Description | kelch-like family member 16kelch-like protein 16 | |
Modification date | 20141222 | |
dbXrefs | MIM : 605379 | |
HGNC : HGNC | ||
HPRD : 05647 | ||
Protein | UniProt: go to UniProt's Cross Reference DB Table | |
Expression | CleanEX: HS_GAN | |
BioGPS: 8139 | ||
Pathway | NCI Pathway Interaction Database: GAN | |
KEGG: GAN | ||
REACTOME: GAN | ||
Pathway Commons: GAN | ||
Context | iHOP: GAN | |
ligand binding site mutation search in PubMed: GAN | ||
UCL Cancer Institute: GAN | ||
Assigned class in TissGDB* | C | |
Included tissue-specific gene expression resources | HPA,GTEx | |
Specific-tissues in normal samples (assigned by TissGDB using HPA, TiGER, and GTEx) | Skin | |
Cancer types related to the specific-tissues in cancer samples (assigned by TissGDB using TCGA) | SKCM | |
Reference showing the relevant tissue of GAN | ||
Description by TissGene annotations | Have significant anti-correlated miRNA |
* 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 | GO:0016567 | protein ubiquitination | 15983046 | GO:0016567 | protein ubiquitination | 15983046 |
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TissGeneExp for GAN |
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) |
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. |
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 |
LUSC | 1.171229398 | -0.46176668 | 1.632996078 | 1.89E-18 | 1.81E-17 |
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TissGene-miRNA for GAN |
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 |
ACC | hsa-miR-497-5p | MIMAT0002820 | 0.026 | -0.27 | 78 |
ACC | hsa-miR-497-5p | MIMAT0002820 | 0.026 | -0.27 | 78 |
LAML | hsa-miR-150-5p | MIMAT0000451 | 0.00033 | -0.27 | 173 |
ACC | hsa-let-7d-5p | MIMAT0000065 | 0.014 | -0.28 | 78 |
ACC | hsa-let-7d-5p | MIMAT0000065 | 0.014 | -0.28 | 78 |
UCS | hsa-miR-190a-5p | MIMAT0000458 | 0.039 | -0.28 | 56 |
UCS | hsa-let-7c-5p | MIMAT0000064 | 0.011 | -0.34 | 56 |
UCS | hsa-miR-137 | MIMAT0000429 | 0.03 | -0.34 | 56 |
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TissGeneMut for GAN |
TissGeneSNV for GAN |
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. |
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) |
- nsSNVs sorted by frequency. |
AAchange | Cancer type | # samples |
p.V189F | LUAD | 2 |
p.P443S | SKCM | 1 |
p.I129V | STAD | 1 |
p.A291V | PAAD | 1 |
p.N352S | HNSC | 1 |
p.G474V | STAD | 1 |
p.I575V | STAD | 1 |
p.S323X | KIRC | 1 |
p.S272F | SKCM | 1 |
p.I251V | STAD | 1 |
p.Y530F | COAD | 1 |
p.R549I | CESC | 1 |
p.S390Y | BRCA | 1 |
p.P562S | SKCM | 1 |
p.Q586* | BLCA | 1 |
p.R567C | UCEC | 1 |
p.S22C | HNSC | 1 |
p.S390C | BLCA | 1 |
p.A261V | COAD | 1 |
p.E168A | LUAD | 1 |
p.R479C | BLCA | 1 |
p.P64L | LUAD | 1 |
p.T70A | PAAD | 1 |
p.A417V | STAD | 1 |
p.R477Q | SKCM | 1 |
p.S492P | PAAD | 1 |
p.K287R | LUAD | 1 |
p.R286Q | OV | 1 |
p.R545C | UCEC | 1 |
p.I73T | OV | 1 |
p.E260G | GBM | 1 |
p.K421N | KIRC | 1 |
p.H213N | UCEC | 1 |
p.E498K | LUAD | 1 |
p.G374V | LUSC | 1 |
p.R201X | READ | 1 |
p.A220S | LUAD | 1 |
p.S323* | KIRC | 1 |
p.M218L | PRAD | 1 |
p.S165G | STAD | 1 |
p.Y61C | LIHC | 1 |
p.D104Y | THYM | 1 |
p.D37H | CESC | 1 |
p.V149I | LGG | 1 |
p.S79L | UCEC | 1 |
p.F29L | LUAD | 1 |
p.S183Y | COAD | 1 |
p.E3K | BLCA | 1 |
p.R566C | KIRP | 1 |
p.Q176E | HNSC | 1 |
p.T489I | HNSC | 1 |
p.R232Q | BLCA | 1 |
p.Y89C | UCEC | 1 |
p.R138G | LUAD | 1 |
p.G280X | ESCA | 1 |
p.H556P | SKCM | 1 |
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TissGeneCNV for GAN |
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 GAN |
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 |
Chimerdb3.0 | ChiTaRs | NA | BQ308823 | RRP1-GAN | chr21:45217839 | chr16:81397417 | |
Chimerdb3.0 | ChiTaRs | NA | AK001100 | MIR100HG-GAN | chr11:122033430 | chr16:81365502 | |
TCGAfusionPortal | PRADA | LUSC | TCGA-18-3412-01A | GAN-GRM7 | Out-of-frame | Chr16:81348885 | Chr3:7188139 |
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TissGeneNet for GAN |
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 GAN |
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 GAN |
TissGeneDrug for GAN |
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 GAN |
Disease information associated with TissGene (DisGeNet, 2016-06-01) |
Disease ID | Disease name | # pubmeds | Source |
umls:C1850386 | GIANT AXONAL NEUROPATHY 1 | 20 | BeFree,CLINVAR,CTD_human,MGD,ORPHANET,UNIPROT |
umls:C0270921 | Axonal neuropathy | 4 | BeFree |
umls:C0598589 | Inherited neuropathies | 2 | BeFree |
umls:C0007959 | Charcot-Marie-Tooth Disease | 1 | BeFree |
umls:C0010823 | Cytomegalovirus Infections | 1 | BeFree |
umls:C0027765 | nervous system disorder | 1 | BeFree |
umls:C0031117 | Peripheral Neuropathy | 1 | CTD_human |
umls:C0040336 | Tobacco Use Disorder | 1 | GAD |
umls:C0345392 | Congenital kyphoscoliosis | 1 | BeFree |
umls:C0442874 | Neuropathy | 1 | BeFree |
umls:C0524851 | Neurodegenerative Disorders | 1 | BeFree |
umls:C0575158 | Kyphoscoliosis deformity of spine | 1 | BeFree |
umls:C0600033 | Acquired Kyphoscoliosis | 1 | BeFree |
umls:C1510586 | Autism Spectrum Disorders | 1 | BeFree |