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Bioinformatics and Systems Medicine Laboratory Bioinformatics and Systems Medicine Laboratory

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TissGeneSummary

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TissGeneExp

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TissGene-miRNA

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TissGeneMut: TissGeneSNV, TissGeneCNV, and TissGeneFusions

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TissGeneNet

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TissGeneProg

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TissGeneClin: TissGeneDrug and TissGeneDisease

TissGeneSummary for SYN1
check button Gene summary
Basic gene informationGene symbolSYN1
Gene namesynapsin I
SynonymsSYN1a|SYN1b|SYNI
CytomapUCSC genome browser: Xp11.23
Type of geneprotein-coding
RefGenesNM_006950.3,
NM_133499.2,
Descriptionbrain protein 4.1synapsin-1
Modification date20141207
dbXrefs MIM : 313440
HGNC : HGNC
Ensembl : ENSG00000008056
HPRD : 02433
Vega : OTTHUMG00000021454
ProteinUniProt:
go to UniProt's Cross Reference DB Table
ExpressionCleanEX: HS_SYN1
BioGPS: 6853
PathwayNCI Pathway Interaction Database: SYN1
KEGG: SYN1
REACTOME: SYN1
Pathway Commons: SYN1
ContextiHOP: SYN1
ligand binding site mutation search in PubMed: SYN1
UCL Cancer Institute: SYN1
Assigned class in TissGDB*C
Included tissue-specific gene expression resourcesHPA,TiGER
Specific-tissues in normal samples (assigned by TissGDB using HPA, TiGER, and GTEx)Brain
Cancer types related to the specific-tissues in cancer samples (assigned by TissGDB using TCGA)GBM,LGG
Reference showing the relevant tissue of SYN1
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.

check button Gene ontology having evidence of Inferred from Direct Assay (IDA) from Entrez
GO IDGO termPubMed ID


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TissGeneExp for SYN1

check button 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 exp


check button 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 isoform exp


check button 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.
normal gene exp


check button 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)
DEG exp

- Significantly differentially expressed cancer types and information. (|Fold change|>1 and FDR<0.05)
Cancer typeMean(exp) in tumorMean(exp) in matched normalLog2FCP-val.FDR
THCA-1.12975478-3.4581107122.3283559321.61E-131.65E-12
LIHC-1.997654305-0.790786305-1.2068680.0005730.001648488


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TissGene-miRNA for SYN1

check button 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 typemiRNA idmiRNA accessionP-val.Coeff.# samples


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TissGeneMut for SYN1
TissGeneSNV for SYN1

check button 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.
SNV lollipop
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check button 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)
SNV distribution

- nsSNVs sorted by frequency.
AAchangeCancer type# samples
p.G396DSKCM2
p.F148LUCEC2
p.G132RSKCM1
p.I363VOV1
p.Q450XLIHC1
p.R234*UCEC1
p.A230TLIHC1
p.T359MUCEC1
p.H188YSTAD1
p.M327ILUAD1
p.E243KUCEC1
p.T448ASTAD1
p.H136NLUAD1
p.I247TREAD1
p.F288LSKCM1
p.K378QCESC1
p.P393LLIHC1
p.G396SSKCM1
p.P63ABLCA1
p.F161LCOAD1
p.R693PSKCM1
p.R420WSTAD1
p.K133NLUAD1
p.H433LLUAD1
p.F130LUCEC1
p.W335*CESC1
p.T298AUCEC1
p.T329AUCEC1
p.A155DBLCA1
p.A371TUCEC1
p.A112PGBM1
p.A155DUCEC1
p.P680ALUAD1
p.E242KLUSC1
p.F13LUCEC1
p.R234QREAD1
p.Y326CCOAD1
p.G380RUCEC1
p.D140GLIHC1
p.A700GLUAD1
p.R693HUCEC1
p.Y252HUCEC1
p.R446HCOAD1
p.N221KLUAD1
p.A208DBRCA1
p.P645LOV1
p.F182CSTAD1
p.K311RSTAD1
p.P33QLUAD1
p.D313NSKCM1
p.T48ITGCT1
p.S177YUCEC1
p.H274RLUAD1


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TissGeneCNV for SYN1

check button 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)
CNV


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TissGeneFusions for SYN1

check button Fusion genes including TissGene
(ChimerDB 3.0, 2016-12-01 and TCGA fusion Portal 2015-12-01)
DatabaseSrcCancer typeSampleFusion geneORF5'-gene BP3'-gene BP
Chimerdb3.0ChiTaRsNABU620269SYN1-GM2AchrX:47446188chr5:150647002
Chimerdb3.0ChiTaRsNACD743038SYN1-DUSP3chrX:47446188chr17:41846479
Chimerdb3.0ChiTaRsNADB258055SYN1-ADAMTS2chrX:47442862chr5:178581638
Chimerdb3.0ChiTaRsNAAI193580SYN1-ALDOCchrX:47446190chr17:26900382
Chimerdb3.0ChiTaRsNADB289761FAM120B-SYN1chr6:170654093chrX:47445377
Chimerdb3.0ChiTaRsNABF948432SYN1-SYN1chrX:47466395chrX:47435924
Chimerdb3.0ChiTaRsNAAW897752SYN1-GAB1chrX:47431866chr4:144285231
Chimerdb3.0ChiTaRsNAAW965197SYN1-RDH14chrX:47446186chr2:18736702
Chimerdb3.0ChiTaRsNABF824769SYN1-PDGFRBchrX:47442882chr5:149505801
Chimerdb3.0ChiTaRsNAAI910121FARP1-SYN1chr13:99059419chrX:47445920
TCGAfusionPortalPRADALGGTCGA-CS-6669-01ASYN1-ATAD13UTR-CDSChrX:47431303Chr10:89552512


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TissGeneNet for SYN1

check button 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)
BRCA (tumor)BRCA (normal)
SYN1, PAK1, PLCG1, PRKACA, CAMK1, ITSN2, PFN2, CAMK2G, EGFR, NOS1AP, SYN2, MAPK3, CDK5, SPTAN1, BIN1, CRK, RASA1, VIM, REST, NOS1, SYN3 (tumor)SYN1, PAK1, KAT5, SRC, PRKACA, CAMK1, SH3GL2, NCF1, PIK3R1, ITSN2, PARK2, PAK2, PFN2, SYN2, MAPK3, CDK5, SPTAN1, BLM, RASA1, REST, SYN3 (normal)
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COAD (tumor)COAD (normal)
SYN1, PAK1, PLCG1, PRKACA, CAMK1, NCF1, PIK3R1, PAK3, PARK2, CAMK2G, SYN2, MAPK3, CDK5, SPTAN1, BIN1, CRK, BLM, S100A1, VIM, AMPH, NOS1 (tumor)SYN1, PAK1, KAT5, PLCG1, GRB2, SRC, PRKACA, CAMK1, SH3GL2, PAK3, PFN2, CAMK2G, SYN2, CDK5, SPTAN1, CRK, S100A1, VIM, AMPH, NOS1, SYN3 (normal)
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HNSC (tumor)HNSC (normal)
SYN1, KAT5, PRKACA, CAMK1, PIK3R1, ITSN2, PAK3, PARK2, PFN2, CAMK2G, EGFR, SYN2, MAPK3, CDK5, BIN1, CRK, BLM, S100A1, VIM, AMPH, NOS1 (tumor)SYN1, PLCG1, GRB2, SRC, PRKACA, CAMK1, SH3GL2, PIK3R1, ITSN2, PAK3, PARK2, PFN2, SYN2, MAPK3, BIN1, CRK, RASA1, S100A1, VIM, AMPH, SYN3 (normal)
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KICH (tumor)KICH (normal)
SYN1, PAK1, GRB2, SRC, PRKACA, NCF1, PIK3R1, PAK3, PARK2, PFN2, CAMK2G, SYN2, CDK5, SPTAN1, BIN1, CRK, BLM, VIM, REST, AMPH, SYN3 (tumor)SYN1, PAK1, PLCG1, SRC, PRKACA, CAMK1, ITSN2, PAK3, PARK2, PAK2, PFN2, EGFR, NOS1AP, SYN2, CDK5, BIN1, CRK, BLM, RASA1, REST, SYN3 (normal)
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KIRC (tumor)KIRC (normal)
SYN1, KAT5, PLCG1, PRKACA, SH3GL2, NCF1, PIK3R1, ITSN2, PAK3, PARK2, PAK2, PFN2, CAMK2G, SYN2, CDK5, SPTAN1, BLM, RASA1, VIM, AMPH, SYN3 (tumor)SYN1, PAK1, KAT5, PLCG1, GRB2, SRC, PRKACA, CAMK1, ITSN2, PAK3, PARK2, PFN2, CAMK2G, SYN2, CDK5, BLM, RASA1, S100A1, VIM, AMPH, SYN3 (normal)
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KIRP (tumor)KIRP (normal)
SYN1, KAT5, PLCG1, SRC, PRKACA, SH3GL2, NCF1, PIK3R1, PAK3, PARK2, PAK2, PFN2, CAMK2G, MAPK3, CDK5, CRK, BLM, VIM, REST, AMPH, NOS1 (tumor)SYN1, PAK1, KAT5, PLCG1, SRC, SH3GL2, PARK2, PAK2, PFN2, CAMK2G, EGFR, NOS1AP, SYN2, MAPK3, CDK5, BIN1, BLM, RASA1, VIM, REST, AMPH (normal)
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LIHC (tumor)LIHC (normal)
SYN1, KAT5, PLCG1, GRB2, SRC, PRKACA, SH3GL2, PIK3R1, PAK2, PFN2, CAMK2G, EGFR, SYN2, CDK5, SPTAN1, BIN1, CRK, RASA1, VIM, REST, AMPH (tumor)SYN1, PAK1, KAT5, SRC, PRKACA, SH3GL2, NCF1, PIK3R1, PAK3, PARK2, PAK2, PFN2, NOS1AP, MAPK3, CDK5, BIN1, BLM, RASA1, S100A1, VIM, AMPH (normal)
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LUAD (tumor)LUAD (normal)
SYN1, PAK1, KAT5, PLCG1, GRB2, SRC, PRKACA, ITSN2, PAK3, PARK2, PAK2, CAMK2G, EGFR, NOS1AP, SYN2, CDK5, SPTAN1, CRK, VIM, REST, AMPH (tumor)SYN1, PAK1, PLCG1, GRB2, SRC, PRKACA, SH3GL2, NCF1, PIK3R1, ITSN2, PAK3, PARK2, PFN2, CAMK2G, EGFR, NOS1AP, SYN2, CDK5, SPTAN1, VIM, AMPH (normal)
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LUSC (tumor)LUSC (normal)
SYN1, PAK1, KAT5, GRB2, SRC, PRKACA, SH3GL2, ITSN2, PAK3, PARK2, PAK2, CAMK2G, NOS1AP, SPTAN1, BIN1, BLM, RASA1, S100A1, VIM, AMPH, SYN3 (tumor)SYN1, KAT5, PLCG1, PRKACA, SH3GL2, PAK3, PARK2, PAK2, PFN2, CAMK2G, EGFR, SYN2, MAPK3, CDK5, SPTAN1, BIN1, BLM, S100A1, VIM, AMPH, SYN3 (normal)
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PRAD (tumor)PRAD (normal)
SYN1, PAK1, PLCG1, GRB2, PRKACA, SH3GL2, NCF1, PARK2, PFN2, CAMK2G, EGFR, SYN2, MAPK3, SPTAN1, BIN1, CRK, RASA1, VIM, REST, AMPH, SYN3 (tumor)SYN1, KAT5, PRKACA, NCF1, ITSN2, PAK3, PARK2, PAK2, CAMK2G, EGFR, NOS1AP, SYN2, MAPK3, SPTAN1, BIN1, RASA1, S100A1, VIM, REST, AMPH, SYN3 (normal)
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STAD (tumor)STAD (normal)
SYN1, KAT5, PLCG1, PRKACA, CAMK1, SH3GL2, PIK3R1, PAK3, PARK2, PFN2, CAMK2G, SYN2, MAPK3, CDK5, SPTAN1, BIN1, BLM, VIM, AMPH, NOS1, SYN3 (tumor)SYN1, PAK1, PLCG1, PRKACA, CAMK1, SH3GL2, PAK3, PARK2, PFN2, CAMK2G, SYN2, CDK5, BIN1, BLM, RASA1, S100A1, VIM, REST, AMPH, NOS1, SYN3 (normal)
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THCA (tumor)THCA (normal)
SYN1, PAK1, KAT5, GRB2, CAMK1, NCF1, ITSN2, PARK2, PAK2, PFN2, EGFR, CDK5, BIN1, CRK, BLM, RASA1, S100A1, VIM, REST, NOS1, SYN3 (tumor)SYN1, SRC, CAMK1, SH3GL2, NCF1, PARK2, PAK2, PFN2, CAMK2G, EGFR, NOS1AP, CDK5, SPTAN1, BIN1, BLM, RASA1, S100A1, VIM, AMPH, NOS1, SYN3 (normal)
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TissGeneProg for SYN1

check button 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.
survival 1

check button 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.
survival 2

check button 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.
survival 3

check button 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.
survival 4

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TissGeneClin for SYN1
TissGeneDrug for SYN1

check button Drug information targeting TissGene
(DrugBank Version 5.0.6, 2017-04-01)
DrugBank IDDrug nameDrug activityDrug typeDrug status


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TissGeneDisease for SYN1

check button Disease information associated with TissGene
(DisGeNet, 2016-06-01)
Disease IDDisease name# pubmedsSource
umls:C0014544Epilepsy5BeFree
umls:C0004352Autistic Disorder3BeFree,MGD
umls:C0035372Rett Syndrome3BeFree
umls:C1510586Autism Spectrum Disorders3BeFree
umls:C0014547Epilepsies, Partial2BeFree
umls:C0027819Neuroblastoma2BeFree
umls:C0036341Schizophrenia2BeFree
umls:C0700095Central neuroblastoma2BeFree
umls:C0002395Alzheimer's Disease1BeFree
umls:C0006142Malignant neoplasm of breast1BeFree
umls:C0011860Diabetes Mellitus, Non-Insulin-Dependent1GAD
umls:C0025202melanoma1BeFree
umls:C0027126Myotonic Dystrophy1BeFree
umls:C0028945oligodendroglioma1BeFree
umls:C0030567Parkinson Disease1GAD
umls:C0178874Tumor Progression1BeFree
umls:C0236642Pick Disease of the Brain1BeFree
umls:C0333463Senile Plaques1BeFree
umls:C0338451Frontotemporal dementia1BeFree
umls:C0391957idiopathic epilepsy1BeFree
umls:C0410226Congenital Myotonic Dystrophy1BeFree
umls:C0454651Specific language impairment1BeFree
umls:C0524528Pervasive Development Disorder1BeFree
umls:C0678222Breast Carcinoma1BeFree
umls:C0751396Well Differentiated Oligodendroglioma1BeFree
umls:C1261473Sarcoma1BeFree
umls:C1845343Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders0CLINVAR,CTD_human,MGD,ORPHANET