EuRBPDB

  • Home
  • Cancer
  • Family
  • Species
  • RBPredictor
  • Search
  • Download
  • Submit
  • Help
  • Contact
TCGA tumor abbreviations
  • ACCAdrenocortical carcinoma
  • BLCABladder Urothelial Carcinoma
  • BRCABreast invasive carcinoma
  • CESCCervical squamous cell carcinoma and endocervical adenocarcinoma
  • CHOLCholangio carcinoma
  • COADColon adenocarcinoma
  • DLBCLymphoid Neoplasm Diffuse Large B-cell Lymphoma
  • ESCAEsophageal carcinoma
  • GBMGlioblastoma multiforme
  • HNSCHead and Neck squamous cell carcinoma
  • KICHKidney Chromophobe
  • KIRCKidney renal clear cell carcinoma
  • KIRPKidney renal papillary cell carcinoma
  • LAMLAcute Myeloid Leukemia
  • LGGBrain Lower Grade Glioma
  • LIHCLiver hepatocellular carcinoma
  • LUADLung adenocarcinoma
  • LUSCLung squamous cell carcinoma
  • MESOMesothelioma
  • OVOvarian serous cystadenocarcinoma
  • PAADPancreatic adenocarcinoma
  • PCPGPheochromocytoma and Paraganglioma
  • PRADProstate adenocarcinoma
  • READRectum adenocarcinoma
  • SARCSarcoma
  • SKCMSkin Cutaneous Melanoma
  • STADStomach adenocarcinoma
  • TGCTThyroid carcinoma
  • THCAThyroid carcinoma
  • THYMThymoma
  • UCECUterine Corpus Endometrial Carcinoma
  • UCSUterine Carcinosarcoma
  • UVMUveal Melanoma

Note: Click here to get the extension of tumor abbreviations.


  • Cancer Related Information
  • Basic Information

Differential Expression

Expression in 33 cancers

Mutations
CancerChrPosition Mutation TypedbSNPProtein-change Allele FreqRBD
BLCAchr6116279380Missense_MutationNAE151K0.31
BLCAchr6116279038Missense_MutationNAL265V0.08
BLCAchr6116279326Missense_MutationNAE169K0.4
BLCAchr61162798755'UTRnovel0.48
BLCAchr6116279386Missense_MutationnovelE149K0.7
BLCAchr6116279212Missense_Mutationrs758399636E207K0.89
BLCAchr6116279363Missense_MutationnovelK156N0.75
BLCAchr6116279479Missense_MutationnovelD118N0.59
BLCAchr6116279046Missense_MutationNAR262P0.2
BLCAchr6116279386Missense_MutationnovelE149Q0.12
BRCAchr61162774653'UTRnovel0.5
BRCAchr6116279518Missense_MutationNAA105T0.12
BRCAchr6116278782Missense_MutationnovelS350C0.3
BRCAchr6116278611Missense_MutationNAY407C0.45
BRCAchr6116278922SilentnovelY303Y0.03
CESCchr6116279528SilentnovelG101G0.3
CESCchr61162773643'UTRnovel0.29
CESCchr6116279429SilentnovelI134I0.45
CESCchr6116279617Missense_MutationnovelQ72K0.42
CESCchr6116279007Missense_MutationNAI275N0.93
CESCchr6116279515Missense_Mutationrs377352006E106K0.48
CESCchr61162771463'UTRnovel0.56
CESCchr6116278980Missense_MutationnovelR284Q0.63
COADchr6116278573Missense_Mutationrs755262799R420C0.32
COADchr6116279779Missense_MutationNAI18F0.56
COADchr6116279109Missense_MutationNAT241I0.23
COADchr6116278981Nonsense_MutationNAR284*0.06
COADchr6116278599Missense_Mutationrs537676463R411H0.42
ESCAchr6116279352Missense_MutationnovelC160F0.26
ESCAchr6116279463Missense_MutationNAK123R0.48
GBMchr6116279536Missense_MutationnovelE99K0.3
GBMchr6116279102Missense_MutationnovelN243K0.14
GBMchr6116279698Missense_MutationnovelV45M0.39
HNSCchr6116278771Missense_MutationnovelP354A0.29
KIRCchr6116278640Frame_Shift_DelnovelK397Rfs*150.28
KIRCchr6116279540Frame_Shift_DelnovelQ98Rfs*170.2
LAMLchr6116278670SilentnovelP387P0.06
LGGchr6116279475Missense_MutationnovelR119H0.29
LIHCchr6116279386Missense_MutationnovelE149Q0.33
LUADchr6116279326Missense_MutationNAE169K0.16
LUADchr61162798595'UTRnovel0.17
LUADchr6116279098Missense_MutationnovelQ245E0.2
LUSCchr6116279716Missense_MutationNAQ39K0.14
LUSCchr6116279592Missense_MutationnovelT80I0.08
OVchr6116278963Nonsense_MutationnovelS290Tfs*20.03
OVchr6116278774Missense_MutationNAT353S0.25
PAADchr6116279618SilentnovelP71P0.07
PRADchr61162798895'UTRnovel0.26
READchr6116278912Missense_MutationnovelL307V0.46
SARCchr6116279542Missense_MutationnovelG97R0.13
SKCMchr6116278886SilentNAP315P0.26
SKCMchr6116278541SilentNAR430R0.23
SKCMchr61162784373'UTRnovel0.39
SKCMchr61162798955'UTRnovel0.5
SKCMchr6116279468SilentnovelL121L0.44
STADchr6116278642Nonsense_MutationnovelK397*0.26
STADchr6116279463Frame_Shift_DelNAK123Rfs*100.13
STADchr6116278923Missense_MutationNAY303C0.04
STADchr6116279346Missense_MutationnovelT162I0.35
STADchr6116278829SilentNAK334K0.26
THCAchr6116279098Nonsense_MutationNAQ245*0.36
UCECchr61162771453'UTRnovel0.33
UCECchr6116279380Missense_MutationNAE151K0.21
UCECchr6116278934Missense_MutationNAE299D0.14
UCECchr6116279463Missense_MutationNAK123R0.24
UCECchr6116278541SilentNAR430R0.21
UCECchr61162771543'UTRrs1925852210.21
UCECchr6116278650Missense_Mutationrs745484190E394G0.36
UCECchr6116279446Nonsense_MutationnovelE129*0.38
UCECchr6116279666Missense_MutationnovelE55D0.58
UCECchr61162771033'UTRnovel0.35
UCECchr6116278658Missense_MutationnovelK391N0.31
UCECchr6116278759Missense_MutationnovelR358C0.05
UCECchr61162773913'UTRnovel0.18
UCECchr61162774053'UTRnovel0.48
UCECchr6116279391Missense_MutationnovelG147E0.12
UCECchr6116279393SilentnovelA146A0.12
UCECchr6116278716Missense_MutationNAD372G0.13
UCECchr6116279678Missense_MutationnovelE51D0.36
UCECchr6116279254Missense_MutationNAE193K0.22
UCECchr6116279031Missense_MutationnovelR267Q0.3
UCECchr61162771463'UTRnovel0.53
UCECchr61162798375'UTRnovel0.42
UCECchr61162772203'UTRnovel0.35

Copy Number Variations (CNVs)
CancerTypeFreq Q-value
BLCADEL0.3753.4915e-05
DLBCDEL0.27080.00052595
ESCADEL0.2120.036953
GBMDEL0.21491.056e-05
KIRCDEL0.2337.439e-11
LGGDEL0.14040.0054594
LUADDEL0.41670.0021365
MESODEL0.43680.05642
PAADDEL0.35870.11274
SKCMDEL0.53411.5442e-06
STADDEL0.13150.0044196
THYMDEL0.13010.10691

Survival Analysis
CancerP-value Q-value
MESO0.00015

Kaplan-Meier Survival Analysis

ACC0.0041

Kaplan-Meier Survival Analysis

HNSC0.046

Kaplan-Meier Survival Analysis

SKCM0.018

Kaplan-Meier Survival Analysis

BRCA0.038

Kaplan-Meier Survival Analysis

KIRP0.023

Kaplan-Meier Survival Analysis

PAAD0.00017

Kaplan-Meier Survival Analysis

DLBC0.039

Kaplan-Meier Survival Analysis

LGG0.0001

Kaplan-Meier Survival Analysis

LUAD0.022

Kaplan-Meier Survival Analysis

UVM0.015

Kaplan-Meier Survival Analysis

OV0.0098

Kaplan-Meier Survival Analysis

Drugs

Select Dataset :


Input Drug :


Input Cell Line :


Eesembl ID



Cell lines and drugs in GSE70138 or GSE92742

  • Description
  • RBPome
  • Expression
  • Transcripts
  • Gene Model
  • PPI
  • Gene Ontology
Description
Ensembl ID
ENSG00000189241 (Gene tree)
Gene ID
7259
Gene Symbol
TSPYL1
Alias
TSPYL
Full Name
TSPY like 1
Gene Type
protein_coding
Species
Homo_sapiens
Status
putative
Strand
Minus strand
Length
5,259 bases
Position
chr6:116,274,859-116,280,117
Accession
12382
RBP type
non-canonical RBP
Summary
The protein encoded by this gene is found in the nucleolus and is similar to that of a family of genes on the Y-chromosome. This gene is intronless. Defects in this gene are a cause of sudden infant death with dysgenesis of the testes syndrome (SIDDT). [provided by RefSeq, Dec 2009]
RNA binding proteome (RBPome)
PIDTitleMethod TimeAuthorDoi
29431736Capturing the interactome of newly transcribed RNARICK & Hela2018 Feb 12Bao XDOI: 10.1038/nmeth.4595
30528433The Human RNA-Binding Proteome and Its Dynamics during Translational ArrestXRNAX & Hela2018 Dec 6Trendel JDOI: 10.1016/j.cell.2018.11.004
Expression
Transcripts
Transcript IDNameLengthRefSeq ID Protein IDLengthRefSeq IDUniportKB ID
ENST00000368608TSPYL1-2013326-ENSP00000357597437 (aa)-Q9H0U9
Gene Model
Click here to download ENSG00000189241's gene model file
Protein-Protein Interaction (PPI)

Clik here to download ENSG00000189241's network
Gene Ontology
Go IDGo_termPubmedIDEvidenceCategory
GO:0005634nucleus-IDAComponent
GO:0005730nucleolus-IDAComponent
GO:0006334nucleosome assembly-IEAProcess
GO:0008150biological_process-NDProcess
GO:0019899enzyme binding23382074.IPIFunction
To top

Copyright © , Bioinformatics Center, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, China. All Rights Reserved.

Any comment and suggestion, please contact us