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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 SLC39A12
check button Gene summary
Basic gene informationGene symbolSLC39A12
Gene namesolute carrier family 39 (zinc transporter), member 12
SynonymsLZT-Hs8|ZIP-12|bA570F3.1
CytomapUCSC genome browser: 10p12.33
Type of geneprotein-coding
RefGenesNM_001145195.1,
NM_001282733.1,NM_001282734.1,NM_152725.3,
DescriptionLIV-1 subfamily of ZIP zinc transporter 8solute carrier family 39 (metal ion transporter), member 12solute carrier family 39 member 12zinc transporter ZIP12zrt- and Irt-like protein 12
Modification date20141207
dbXrefs MIM : 608734
HGNC : HGNC
Ensembl : ENSG00000148482
HPRD : 15384
Vega : OTTHUMG00000017759
ProteinUniProt:
go to UniProt's Cross Reference DB Table
ExpressionCleanEX: HS_SLC39A12
BioGPS: 221074
PathwayNCI Pathway Interaction Database: SLC39A12
KEGG: SLC39A12
REACTOME: SLC39A12
Pathway Commons: SLC39A12
ContextiHOP: SLC39A12
ligand binding site mutation search in PubMed: SLC39A12
UCL Cancer Institute: SLC39A12
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 SLC39A12
Description by TissGene annotationsTissgsKTS
CNV lost TissGeneKTS
* 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 SLC39A12

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-0.290501893-1.404952741.1144508472.53E-069.08E-06


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TissGene-miRNA for SLC39A12

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 SLC39A12
TissGeneSNV for SLC39A12

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.E126KSKCM2
p.G453*LUAD2
p.G368SSKCM2
p.I194MSKCM1
p.V49ILUAD1
p.E495KLIHC1
p.L399FCOAD1
p.L316VLUSC1
p.Y367FHNSC1
p.I577MLUAD1
p.E318DUCEC1
p.E70KSKCM1
p.Q286*SKCM1
p.A432DLUSC1
p.E395KLUAD1
p.R77KLUAD1
p.S192FSKCM1
p.R107GLUAD1
p.R62KCOAD1
p.L377RCOAD1
p.S10FBLCA1
p.L46MLUAD1
p.C85YBLCA1
p.K323NLUAD1
p.A416TCOAD1
p.L467VHNSC1
p.T635ILUSC1
p.L425FTHYM1
p.C628YLIHC1
p.E331DLUAD1
p.L451*LUAD1
p.L50ICOAD1
p.P433TLUAD1
p.D473GSTAD1
p.G596ESKCM1
p.E431*LUAD1
p.W632*SKCM1
p.K138ELIHC1
p.H428LHNSC1
p.E331*LUAD1
p.R660LLUAD1
p.G368CHNSC1
p.S8LBLCA1
p.E90DHNSC1
p.R352KUCEC1
p.Q125HSKCM1
p.A529SCOAD1
p.Y369CLUAD1
p.G193*ACC1
p.D473NSKCM1
p.S645FLUAD1
p.W676CHNSC1
p.S160XSTAD1
p.V220IESCA1
p.D516NPAAD1
p.S526ILUAD1
p.L646FLUAD1
p.L96IPRAD1
p.L593FLUAD1
p.D285NSKCM1
p.T574RSKCM1
p.E581VESCA1
p.G450ESKCM1
p.M522ILUAD1
p.E394DPRAD1
p.A98DHNSC1
p.G453VLUAD1
p.G193XACC1
p.C221FHNSC1
p.S565*LUAD1
p.I559TLUAD1
p.G454VLUAD1
p.S565LSKCM1
p.Q322RLUAD1
p.K270NUCEC1
p.K132NLUAD1
p.P230LLUAD1
p.S8LHNSC1
p.V9LLUAD1
p.K330NLUAD1
p.S513ILUSC1
p.E109*UCEC1
p.Y369HBLCA1
p.S229FBLCA1
p.S156FHNSC1
p.L672FBLCA1
p.S178FLUAD1
p.K141TUCEC1
p.E154KLIHC1
p.R314SSTAD1
p.E318KSKCM1
p.G450ELUAD1
p.R243HSTAD1
p.L642SESCA1
p.N290KBLCA1
p.H124QCOAD1
p.S8LTHCA1
p.Y174FESCA1
p.A93SLUAD1
p.G384EHNSC1
p.G223VLUSC1
p.P338TLUAD1
p.Q254KLUAD1
p.C310SLIHC1
p.T574MSTAD1
p.T528RKIRC1
p.F291LLUAD1
p.Y618HSTAD1
p.K6NHNSC1
p.L68SLUAD1
p.G199SSKCM1
p.G453LLUAD1
p.D104YLUSC1
p.F670LSTAD1
p.M615IBRCA1
p.L679ILUAD1
p.F3LLUAD1
p.S197ILUAD1
p.E331VESCA1
p.V374ISTAD1
p.E365DHNSC1
p.S149CLUAD1
p.Q112ELUAD1
p.R113SESCA1
p.L345VLUAD1
p.T204MUCEC1
p.H391NKIRC1
p.L667MHNSC1
p.S566LBLCA1
p.G223ESKCM1
p.E235DLIHC1
p.E331KSKCM1
p.W632XSKCM1
p.I577VBRCA1
p.N226DLUSC1
p.D301YLUAD1
p.E318*LUAD1
p.D166GSTAD1
p.H124YSKCM1
p.G80RSKCM1
p.S160*STAD1
p.D415EBLCA1
p.G436WLUAD1
p.T385ALGG1
p.E163KSKCM1
p.L401*OV1
p.S598CLUAD1
p.H284NLUAD1
p.I524KSKCM1
p.G457EBLCA1
p.M382ISTAD1
p.W662*SKCM1
p.Q173HLUAD1
p.S23FSKCM1
p.P583TLUSC1
p.H439LLUAD1
p.R248HUCEC1
p.E154DSTAD1
p.Q286XSKCM1
p.S178YLUSC1
p.L399ILUAD1
p.330_331KE>N*LUAD1
p.W306*SKCM1
p.A31TBRCA1
p.H439QLUAD1
p.N280SBLCA1
p.S337CLIHC1
p.V591MPAAD1
p.F614SBLCA1
p.D33VSKCM1


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TissGeneCNV for SLC39A12

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 SLC39A12

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


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TissGeneNet for SLC39A12

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)


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TissGeneProg for SLC39A12

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 SLC39A12
TissGeneDrug for SLC39A12

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 SLC39A12

check button Disease information associated with TissGene
(DisGeNet, 2016-06-01)
Disease IDDisease name# pubmedsSource
umls:C0020538Hypertensive disease1GAD
umls:C0020542Pulmonary Hypertension1BeFree
umls:C0021390Inflammatory Bowel Diseases1GAD
umls:C0025202melanoma1CTD_human
umls:C0040336Tobacco Use Disorder1GAD
umls:C0376358Malignant neoplasm of prostate1GAD
umls:C1271104Blood pressure finding1GAD
umls:C1272641Systemic arterial pressure1GAD