EuRBPDB

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  • Basic Information
  • Cancer Related Information

  • Description
  • RBPome
  • Literatures
  • Expression
  • Transcripts
  • Gene Model
  • Phenotypes
  • PPI
  • Gene Ontology
Description
Ensembl ID
ENSG00000107438 (Gene tree)
Gene ID
9124
Gene Symbol
PDLIM1
Alias
CLP-36|hCLIM1|CLP36|CLIM1
Full Name
PDZ and LIM domain 1
Gene Type
protein_coding
Species
Homo_sapiens
Status
confidence
Strand
Minus strand
Length
53,581 bases
Position
chr10:95,237,568-95,291,148
Accession
2067
RBP type
non-canonical RBP
Summary
This gene encodes a member of the enigma protein family. The protein contains two protein interacting domains, a PDZ domain at the amino terminal end and one to three LIM domains at the carboxyl terminal. It is a cytoplasmic protein associated with the cytoskeleton. The protein may function as an adapter to bring other LIM-interacting proteins to the cytoskeleton. Pseudogenes associated with this gene are located on chromosomes 3, 14 and 17. [provided by RefSeq, Oct 2012]
RNA binding proteome (RBPome)
PIDTitleMethod TimeAuthorDoi
30607034Comprehensive identification of RNA protein interactions in any organism using orthogonal organic phase separation (OOPS)OOPS & HEK2932019 Jan 3Queiroz RMLDOI: 10.1038/s41587-018-0001-2
30607034Comprehensive identification of RNA protein interactions in any organism using orthogonal organic phase separation (OOPS)OOPS & MCF10A2019 Jan 3Queiroz RMLDOI: 10.1038/s41587-018-0001-2

Literatures on RNA binding capacity
PIDTitleArticle TimeAuthorDoi
17068759Identification and analysis of altered alpha1,6-fucosylated glycoproteins associated with hepatocellular carcinoma metastasis.Proteomics2006 NovDai Z-
Expression
Transcripts
Transcript IDNameLengthRefSeq ID Protein IDLengthRefSeq IDUniportKB ID
ENST00000493949PDLIM1-205795--- (aa)--
ENST00000329399PDLIM1-2011452XM_011540330ENSP00000360305329 (aa)XP_011538632O00151
ENST00000490391PDLIM1-203458--- (aa)--
ENST00000477757PDLIM1-202850--- (aa)--
ENST00000492511PDLIM1-204453--- (aa)--
Gene Model
Click here to download ENSG00000107438's gene model file
Phenotypes
ensgIDTraitpValuePubmed ID
ENSG00000107438Body Weight9.0130000E-005-
ENSG00000107438Platelet Function Tests3.0608000E-005-
ENSG00000107438Platelet Function Tests2.5482400E-005-
ENSG00000107438Platelet Function Tests3.2294900E-005-
ENSG00000107438Platelet Function Tests1.1193000E-006-
ENSG00000107438Platelet Function Tests1.2040000E-006-
Protein-Protein Interaction (PPI)

Clik here to download ENSG00000107438's network

* RBP PPI network refers to all genes directly bind to RBP
Gene Ontology
Go IDGo_termPubmedIDEvidenceCategory
GO:0001666response to hypoxia-IEAProcess
GO:0003713transcription coactivator activity-IEAFunction
GO:0005667transcription factor complex-IEAComponent
GO:0005856cytoskeleton-IEAComponent
GO:0005913cell-cell adherens junction25468996.HDAComponent
GO:0005925focal adhesion21423176.HDAComponent
GO:0006355regulation of transcription, DNA-templated-IEAProcess
GO:0006979response to oxidative stress8522188.TASProcess
GO:0030018Z disc-IEAComponent
GO:0046872metal ion binding-IEAFunction
GO:0098609cell-cell adhesion-IEAProcess
GO:0098641cadherin binding involved in cell-cell adhesion25468996.HDAFunction
GO:1903508positive regulation of nucleic acid-templated transcription-IEAProcess

Cancer associated literatures
PIDTitleArticle TimeAuthorDoi
26119933Glioma invasion mediated by the p75 neurotrophin receptor (p75(NTR)/CD271) requires regulated interaction with PDLIM1.Oncogene2016 Mar 17Ahn BYdoi: 10.1038/onc.2015.199
24662836PDZ and LIM domain protein 1(PDLIM1)/CLP36 promotes breast cancer cell migration, invasion and metastasis through interaction with α-actinin.Oncogene2015 Mar 5Liu Zdoi: 10.1038/onc.2014.64
26701804PDLIM1 Stabilizes the E-Cadherin/β-Catenin Complex to Prevent Epithelial-Mesenchymal Transition and Metastatic Potential of Colorectal Cancer Cells.Cancer Res2016 Mar 1Chen HNdoi: 10.1158/0008-5472.CAN-15-1962
27068564Autoantibodies against TYMS and PDLIM1 proteins detected as circulatory signatures in Indian breast cancer patients.Proteomics Clin Appl2016 MayGupta Pdoi: 10.1002/prca.201500138.

Differential Expression

Expression in 33 cancers

Mutations
CancerChrPosition Mutation TypedbSNPProtein-change Allele FreqRBD
BLCAchr1095263903Missense_MutationnovelS165L0.38
BLCAchr1095264008Missense_MutationnovelS130W0.17
BRCAchr1095238622Missense_Mutationrs374874749S250L0.15
BRCAchr1095247339Missense_MutationNAS187R0.38
BRCAchr1095268787SilentNAS108S0.18
CESCchr10952909255'UTRrs7770911010.32
CESCchr10952909655'UTRnovel0.67
CESCchr1095247329Missense_Mutationrs151177027D191N0.28
CESCchr1095271764Silentrs759916547A39A0.4
COADchr1095263888Missense_MutationNAS170N0.28
COADchr1095247306Missense_MutationNAK198N0.37
COADchr1095271739Missense_MutationNAD48Y0.35
COADchr1095271746SilentNAC45C0.34
COADchr1095247329Missense_Mutationrs151177027D191N0.47
COADchr1095263951Missense_MutationnovelG149D0.33
COADchr1095264007Silentrs764741236S130S0.3
COADchr1095263864Missense_MutationnovelP178L0.19
COADchr1095263967Missense_MutationNAY144H0.41
COADchr1095271692Missense_MutationNAH63Q0.34
COADchr1095237930Frame_Shift_InsnovelK329Qfs*70.27
COADchr1095238059Missense_MutationNAC286R0.4
COADchr10952378743'UTRnovel0.18
DLBCchr1095238682Missense_MutationnovelD230G0.2
ESCAchr1095238649Missense_MutationnovelK241R0.44
GBMchr1095238577Missense_MutationnovelT265N0.18
GBMchr1095271658Missense_MutationnovelD75N0.23
HNSCchr1095290829Silentrs775650719A29A0.29
HNSCchr1095268788Missense_MutationNAS108F0.25
KIRCchr1095238620Missense_MutationNAI251F0.33
KIRPchr1095238656Missense_MutationNAS239R0.36
LGGchr10952378033'UTRnovel0.5
LGGchr1095268790SilentnovelA107A0.14
LUADchr1095268778Missense_MutationnovelQ111H0.13
LUSCchr1095247258Silentrs762617070T214T0.17
LUSCchr1095290843Nonsense_MutationnovelE25*0.42
LUSCchr1095247314Frame_Shift_DelnovelV196Ffs*110.28
OVchr1095247278Missense_MutationNAE208K0.14
OVchr1095263885Missense_MutationNAG171V0.19
READchr1095247270Silentrs141682059P210P0.5
SKCMchr1095263970Nonsense_MutationnovelQ143*0.33
SKCMchr1095247234SilentNAI222I0.33
SKCMchr1095268825Missense_MutationNAE96K0.8
SKCMchr1095238665Missense_MutationnovelG236R0.33
SKCMchr1095264034SilentnovelN121N0.44
SKCMchr1095271675Missense_MutationNAR69K0.43
SKCMchr1095238616Missense_MutationNAG252E0.31
SKCMchr1095271715Missense_MutationNAE56K0.38
SKCMchr1095238622Missense_Mutationrs374874749S250L0.55
SKCMchr1095263937Missense_MutationNAE154K0.12
SKCMchr1095268820SilentNAG97G0.4
SKCMchr1095271646Missense_MutationNAL79F0.43
SKCMchr1095247215Missense_MutationNAG229R0.14
SKCMchr1095238616Missense_MutationNAG252E0.23
SKCMchr1095247349Missense_MutationNAP184L0.38
SKCMchr1095268788Missense_MutationNAS108F0.09
SKCMchr1095237955SilentNAG320G0.18
SKCMchr1095271646Missense_MutationNAL79I0.31
STADchr1095290854Missense_MutationNAG21D0.28
STADchr1095238013Missense_MutationNAV301A0.28
STADchr1095237981Missense_MutationnovelR312W0.13
STADchr1095271777Missense_MutationnovelP35H0.2
TGCTchr1095238104Missense_MutationnovelF271L0.48
THCAchr10952909345'UTRnovel0.22
UCECchr1095247270Silentrs141682059P210P0.46
UCECchr1095237966Missense_MutationnovelP317S0.43
UCECchr1095237959Missense_MutationnovelE319A0.42
UCECchr1095271636Missense_MutationnovelA82V0.37
UCECchr10952377303'UTRnovel0.33
UCECchr1095264032Missense_MutationNAR122Q0.27
UCECchr1095247270Silentrs141682059P210P0.39
UCECchr1095237974Missense_Mutationrs752319886R314Q0.26
UCECchr1095247258Silentrs762617070T214T0.17
UCECchr1095264032Missense_MutationNAR122Q0.54
UCECchr1095237980Missense_MutationnovelR312Q0.46
UCECchr1095247237Missense_MutationnovelE221D0.27
UCECchr1095238621Silentrs371730712S250S0.31
UCECchr1095238625Missense_Mutationrs565368926A249V0.42
UCECchr1095238053Missense_MutationnovelD288N0.25
UCECchr1095238080Missense_Mutationrs768989089R279C0.4
UCECchr1095264012Missense_Mutationrs377056135A129T0.31
UCECchr1095247270Silentrs141682059P210P0.13
UCECchr1095238621Silentrs371730712S250S0.41
UCECchr1095238617Missense_Mutationrs766930662G252R0.35
UCECchr1095247270Silentrs141682059P210P0.26
UCECchr10952377553'UTRrs5558891250.58
UCECchr1095247258Silentrs762617070T214T0.28
UCECchr1095268815Missense_Mutationrs141713061R99H0.25
UCECchr1095263863Splice_Siters778264797X178_splice0.09
UCECchr1095238625Missense_Mutationrs565368926A249V0.31

Copy Number Variations (CNVs)
CancerTypeFreq Q-value
ACCDEL0.10.19593
CHOLDEL0.16670.048655
COADDEL0.17299.4741e-07
MESODEL0.27590.00015289
PAADDEL0.13040.169
READDEL0.24240.014135
THCADEL0.0160.011063
THYMDEL0.03250.10563
UCSDEL0.30360.1218

Survival Analysis
CancerP-value Q-value
THYM0.03

Kaplan-Meier Survival Analysis

SARC0.027

Kaplan-Meier Survival Analysis

MESO0.00026

Kaplan-Meier Survival Analysis

KIRP0.016

Kaplan-Meier Survival Analysis

CESC0.017

Kaplan-Meier Survival Analysis

LAML0.015

Kaplan-Meier Survival Analysis

UCEC0.00021

Kaplan-Meier Survival Analysis

GBM0.023

Kaplan-Meier Survival Analysis

LGG0.0001

Kaplan-Meier Survival Analysis

CHOL0.033

Kaplan-Meier Survival Analysis

THCA0.032

Kaplan-Meier Survival Analysis

UVM0.00015

Kaplan-Meier Survival Analysis

OV0.013

Kaplan-Meier Survival Analysis

Drugs

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Eesembl ID



Cell lines and drugs in GSE70138 or GSE92742


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