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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 PLP1
check button Gene summary
Basic gene informationGene symbolPLP1
Gene nameproteolipid protein 1
SynonymsGPM6C|HLD1|MMPL|PLP|PLP/DM20|PMD|SPG2
CytomapUCSC genome browser: Xq22
Type of geneprotein-coding
RefGenesNM_000533.3,
NM_001128834.1,NM_199478.1,
Descriptionlipophilinmajor myelin proteolipid proteinmyelin proteolipid protein
Modification date20141219
dbXrefs MIM : 300401
HGNC : HGNC
Ensembl : ENSG00000123560
HPRD : 02321
Vega : OTTHUMG00000022111
ProteinUniProt:
go to UniProt's Cross Reference DB Table
ExpressionCleanEX: HS_PLP1
BioGPS: 5354
PathwayNCI Pathway Interaction Database: PLP1
KEGG: PLP1
REACTOME: PLP1
Pathway Commons: PLP1
ContextiHOP: PLP1
ligand binding site mutation search in PubMed: PLP1
UCL Cancer Institute: PLP1
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 PLP1
Description by TissGene annotationsHave significant anti-correlated miRNA
Fused withTSGene
Fused withOncogene
* 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 PLP1

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
LIHC-4.494249521-1.859117521-2.6351322.05E-179.69E-16
HNSC-2.1581620321.300696107-3.458858142.82E-128.81E-11
LUAD-3.7792569-1.765017245-2.0142396559.81E-148.66E-13
COAD-1.8781732133.939530633-5.8177038464.72E-175.44E-15
PRAD0.9298806332.811072941-1.8811923083.41E-094.75E-08
KIRP-3.872662396-1.271465521-2.6011968753.21E-103.32E-09
BLCA-2.3044997313.313605532-5.6181052631.08E-102.67E-08
STAD-1.4488092713.236178229-4.68498751.18E-112.21E-09
BRCA-1.0261523632.482458163-3.5086105261.31E-322.00E-31
KIRC-3.983680799-1.148787743-2.8348930561.82E-191.36E-18
THCA-2.0230884020.083672615-2.1067610172.44E-071.01E-06
ESCA-2.6125791572.977220843-5.58981.08E-060.000542656


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TissGene-miRNA for PLP1

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
THYMhsa-miR-29b-3pMIMAT00001000.00075-0.3122


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TissGeneMut for PLP1
TissGeneSNV for PLP1

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.T106ALIHC2
p.R137WSTAD2
p.L46QREAD1
p.A248EBRCA1
p.T75SUCEC1
p.S253FSKCM1
p.Q131EHNSC1
p.W145XLIHC1
p.P190TBLCA1
p.F26LUCS1
p.V267IUCEC1
p.V267ISTAD1
p.A115TLUAD1
p.G221VLUSC1
p.Q131ECESC1
p.G125SUCEC1
p.P211SLGG1
p.C139SLUAD1
p.A21VLGG1
p.W181CLIHC1
p.T116MSTAD1
p.R273QPRAD1
p.E44KUCS1
p.H140RLUAD1
p.P176SLGG1
p.R137WOV1
p.W163CLUAD1
p.R273QLUAD1
p.R137QCOAD1
p.L165PLUSC1
p.S218FSKCM1
p.F51LUCS1
p.A115TCOAD1


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TissGeneCNV for PLP1

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 PLP1

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
Chimerdb3.0ChiTaRsNADA174856PLP1-GNPATchrX:103031891chr1:231410993
Chimerdb3.0ChiTaRsNADA387913EPAS1-PLP1chr2:46524725chrX:103031798
Chimerdb3.0ChiTaRsNAAV723721PLP1-MAN2A2chrX:103045735chr15:91464074
Chimerdb3.0ChiTaRsNAAA348328PRRG1-PLP1chrX:37285177chrX:103043392
Chimerdb3.0ChiTaRsNACR740283PLP1-PLP1chrX:103046888chrX:103046981
Chimerdb3.0ChiTaRsNADA415824PTTG1IP-PLP1chr21:46285138chrX:103031845
Chimerdb3.0ChiTaRsNAES316348MRPL10-PLP1chr17:45901092chrX:103045970
Chimerdb3.0ChiTaRsNADA386793RNU12-PLP1chr22:43011399chrX:103031768
Chimerdb3.0ChiTaRsNADA327340OAZ1-PLP1chr19:2269577chrX:103031802
Chimerdb3.0ChiTaRsNADB171847MBNL2-PLP1chr13:97882117chrX:103031802
TCGAfusionPortalPRADALGGTCGA-HT-7902-01APLP1-SGK1NAChrX:103047545Chr6:134639049


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TissGeneNet for PLP1

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)
PLP1, MBP, ITGAV, CALR, CANX, MAG, ITGA5 (tumor)PLP1, MBP, ITGAV, CALR, CANX, MAG, ITGA5 (normal)
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COAD (tumor)COAD (normal)
PLP1, MBP, ITGAV, CALR, CANX, MAG, ITGA5 (tumor)PLP1, MBP, ITGAV, CALR, CANX, MAG, ITGA5 (normal)
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HNSC (tumor)HNSC (normal)
PLP1, MBP, ITGAV, CALR, CANX, MAG, ITGA5 (tumor)PLP1, MBP, ITGAV, CALR, CANX, MAG, ITGA5 (normal)
bullet pointbullet point
KICH (tumor)KICH (normal)
PLP1, MBP, ITGAV, CALR, CANX, MAG, ITGA5 (tumor)PLP1, MBP, ITGAV, CALR, CANX, MAG, ITGA5 (normal)
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KIRC (tumor)KIRC (normal)
PLP1, MBP, ITGAV, CALR, CANX, MAG, ITGA5 (tumor)PLP1, MBP, ITGAV, CALR, CANX, MAG, ITGA5 (normal)
bullet pointbullet point
KIRP (tumor)KIRP (normal)
PLP1, MBP, ITGAV, CALR, CANX, MAG, ITGA5 (tumor)PLP1, MBP, ITGAV, CALR, CANX, MAG, ITGA5 (normal)
bullet pointbullet point
LIHC (tumor)LIHC (normal)
PLP1, MBP, ITGAV, CALR, CANX, MAG, ITGA5 (tumor)PLP1, MBP, ITGAV, CALR, CANX, MAG, ITGA5 (normal)
bullet pointbullet point
LUAD (tumor)LUAD (normal)
PLP1, MBP, ITGAV, CALR, CANX, MAG, ITGA5 (tumor)PLP1, MBP, ITGAV, CALR, CANX, MAG, ITGA5 (normal)
bullet pointbullet point
LUSC (tumor)LUSC (normal)
PLP1, MBP, ITGAV, CALR, CANX, MAG, ITGA5 (tumor)PLP1, MBP, ITGAV, CALR, CANX, MAG, ITGA5 (normal)
bullet pointbullet point
PRAD (tumor)PRAD (normal)
PLP1, MBP, ITGAV, CALR, CANX, MAG, ITGA5 (tumor)PLP1, MBP, ITGAV, CALR, CANX, MAG, ITGA5 (normal)
bullet pointbullet point
STAD (tumor)STAD (normal)
PLP1, MBP, ITGAV, CALR, CANX, MAG, ITGA5 (tumor)PLP1, MBP, ITGAV, CALR, CANX, MAG, ITGA5 (normal)
bullet pointbullet point
THCA (tumor)THCA (normal)
PLP1, MBP, ITGAV, CALR, CANX, MAG, ITGA5 (tumor)PLP1, MBP, ITGAV, CALR, CANX, MAG, ITGA5 (normal)
bullet pointbullet point


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TissGeneProg for PLP1

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 PLP1
TissGeneDrug for PLP1

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 PLP1

check button Disease information associated with TissGene
(DisGeNet, 2016-06-01)
Disease IDDisease name# pubmedsSource
umls:C0205711Pelizaeus-Merzbacher Disease147BeFree,CLINVAR,CTD_human,LHGDN,MGD,UNIPROT
umls:C0751604Hereditary X-Linked Recessive Spastic Paraplegia22BeFree
umls:C0023520Leukodystrophy13BeFree,GAD
umls:C1839264SPASTIC PARAPLEGIA 2, X-LINKED (disorder)10CLINVAR,CTD_human,MGD,ORPHANET,UNIPROT
umls:C0037772Spastic Paraplegia7BeFree
umls:C0014072Experimental Autoimmune Encephalomyelitis6BeFree
umls:C0036341Schizophrenia5BeFree,LHGDN
umls:C0028738Nystagmus4BeFree
umls:C0026769Multiple Sclerosis3BeFree
umls:C0026838Muscle Spasticity3BeFree
umls:C0027765nervous system disorder3BeFree
umls:C0036572Seizures3BeFree,RGD
umls:C0037773Spastic Paraplegia, Hereditary3BeFree
umls:C0524851Neurodegenerative Disorders3BeFree
umls:C0007682CNS disorder2BeFree
umls:C0007789Cerebral Palsy2BeFree,LHGDN
umls:C0026827Muscle hypotonia2BeFree
umls:C0030486Paraplegia2LHGDN
umls:C0031117Peripheral Neuropathy2BeFree
umls:C0037771Paraparesis, Spastic2BeFree
umls:C0235946Cerebral atrophy2BeFree
umls:C0424605Developmental delay (disorder)2BeFree
umls:C0443306Spastic2BeFree
umls:C1269683Major Depressive Disorder2BeFree
umls:C0004114Astrocytoma1BeFree
umls:C0004352Autistic Disorder1BeFree
umls:C0009171Cocaine Abuse1BeFree
umls:C0011265Presenile dementia1BeFree
umls:C0011303Demyelinating Diseases1BeFree
umls:C0020630Hypophosphatasia1BeFree
umls:C0021368Inflammation1LHGDN
umls:C0022661Kidney Failure, Chronic1BeFree
umls:C0033626Protein Deficiency1BeFree
umls:C0034152Henoch-Schoenlein Purpura1BeFree
umls:C0034372Quadriplegia1LHGDN
umls:C0037019Shy-Drager Syndrome1BeFree
umls:C0041696Unipolar Depression1BeFree
umls:C0085078Lysosomal Storage Diseases1BeFree
umls:C0221026X-linked agammaglobulinemia1BeFree
umls:C0268164Primary hyperoxaluria, type I1BeFree
umls:C0270921Axonal neuropathy1BeFree
umls:C0270922Peripheral demyelinating neuropathy1BeFree
umls:C0271388Pendular Nystagmus1BeFree
umls:C0393571Multiple System Atrophy1BeFree
umls:C0393665Multiple Sclerosis, Chronic Progressive1LHGDN
umls:C0442874Neuropathy1BeFree
umls:C0497327Dementia1BeFree
umls:C0598608Hyperhomocysteinemia1BeFree
umls:C0751964Multiple Sclerosis, Primary Progressive1BeFree
umls:C0751967Multiple Sclerosis, Relapsing-Remitting1BeFree
umls:C1263857Peripheral axonal neuropathy1BeFree
umls:C1274795Urban Schosser Spohn syndrome1BeFree
umls:C1709246Non-Neoplastic Disorder1BeFree
umls:C1846058Lubs X-linked mental retardation syndrome1BeFree
umls:C1849156Spastic Ataxia1BeFree
umls:C2316810Chronic kidney disease stage 51BeFree
umls:C3495426Homocysteinemia1BeFree
umls:C3711376Isodicentric Chromosome 15 Syndrome1BeFree
umls:C0751915Pelizaeus-Merzbacher Disease, Atypical0CLINVAR
umls:C0751916Classic Pelizaeus-Merzbacher Disease0ORPHANET
umls:C0751917Pelizaeus-Merzbacher Disease, Transitional0ORPHANET