EuRBPDB

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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
ACCchr774235601SilentnovelI295I0.33
BLCAchr774249112Missense_MutationnovelP78S0.78
BLCAchr774249085Missense_MutationnovelL87V0.21
BLCAchr774232132Nonsense_MutationnovelK347*0.39
BLCAchr774252436Missense_MutationnovelR59T0.22
BLCAchr774232156Missense_MutationnovelG339S0.25
BRCAchr774254355Missense_MutationnovelA10V0.67
CESCchr774232120Missense_MutationNAP351A0.12
CESCchr774238960Nonsense_MutationnovelS241*0.21
CESCchr774243201SilentnovelI160I0.18
CESCchr7742320893'UTRnovel0.09
CESCchr774238932Silentrs782013788N250N0.26
CESCchr774246746Missense_MutationnovelR117M0.41
CHOLchr774246734Missense_MutationnovelK121T0.52
COADchr774240048Missense_MutationnovelD195N0.34
COADchr774240012Missense_Mutationrs548294232E207K0.09
COADchr774254346Missense_MutationnovelV13A0.46
COADchr774232136Nonsense_MutationnovelC345*0.11
GBMchr774243180Silentrs782042572F167F0.22
GBMchr774240012Missense_Mutationrs548294232E207K0.53
GBMchr774240075Missense_MutationnovelA186T0.07
GBMchr774249013Splice_RegionnovelR111R0.18
GBMchr7742320753'UTRnovel0.27
GBMchr774237379Missense_MutationnovelI275L0.18
GBMchr774232114Missense_MutationnovelA353T0.05
HNSCchr774249057Missense_MutationnovelP96L0.19
HNSCchr774235642Missense_MutationnovelL282F0.36
HNSCchr774232174Missense_MutationnovelS333A0.25
KIRCchr774246724SilentNAA124A0.37
KIRCchr774240020Missense_MutationnovelN204S0.25
LIHCchr774239967Missense_MutationnovelI222V0.37
LIHCchr774243204Missense_MutationnovelE159D0.49
LIHCchr774249106Missense_MutationnovelT80S0.28
LUADchr7742320253'UTRnovel0.35
LUADchr774246747Missense_MutationnovelR117G0.18
LUADchr774249756Missense_MutationNAP70A0.17
LUADchr774254341Missense_MutationNAA15S0.41
LUADchr774254363SilentNAC7C0.3
LUADchr774235631Missense_MutationNAL285F0.39
LUSCchr774238937Missense_MutationnovelE249Q0.27
LUSCchr774238937Missense_MutationnovelE249Q0.24
OVchr774237371Missense_MutationnovelE277D0.04
OVchr774235609Frame_Shift_DelnovelE293Kfs*200.1
PAADchr774249740Missense_MutationnovelA75V0.05
SARCchr774239941SilentnovelR230R0.21
SKCMchr774232120Missense_MutationNAP351S0.48
SKCMchr774238969Missense_MutationNAS238F0.22
SKCMchr7742319773'UTRnovel0.36
SKCMchr7742320943'UTRnovel0.11
SKCMchr774254286Missense_MutationnovelH33L0.14
SKCMchr7742544005'UTRnovel0.3
SKCMchr774232119Missense_Mutationrs139636296P351L0.25
SKCMchr774232120Missense_MutationNAP351S0.25
STADchr774232188Missense_Mutationrs41272921A328V0.24
STADchr774235529Splice_Regionrs3693836980.39
STADchr774240012Missense_Mutationrs548294232E207K0.27
STADchr774232123Missense_MutationnovelA350T0.05
STADchr774232187Silentrs377161147A328A0.21
UCECchr7742320743'UTRnovel0.32
UCECchr774239976Nonsense_MutationNAE219*0.14
UCECchr774243179Missense_MutationNAA168T0.24
UCECchr774237373Missense_Mutationrs781977542E277K0.14
UCECchr774240052SilentNAL193L0.14
UCECchr774243217Missense_MutationNAR155M0.49
UCECchr774249027Missense_Mutationrs781895699N106S0.4
UCECchr774243160Missense_MutationnovelS174L0.17
UCECchr774243145Splice_SitenovelX179_splice0.34
UCECchr774240065Missense_MutationnovelR189Q0.35
UCECchr774243239Missense_MutationnovelD148N0.41
UCECchr774252443Missense_MutationNAV57M0.32
UCECchr7742319693'UTRnovel0.29
UCECchr774246740Missense_Mutationrs148234405K119T0.14
UCECchr774232217Splice_SitenovelX319_splice0.38
UCECchr774235638Missense_Mutationrs782546413A283V0.13
UCECchr774239958Missense_MutationnovelA225T0.34
UCECchr774237421Missense_MutationnovelL261M0.47
UCECchr7742319693'UTRnovel0.57
UCECchr774249085Missense_MutationnovelL87M0.2
UCECchr774235610SilentnovelP292P0.41
UCECchr774232188Missense_Mutationrs41272921A328V0.09
UCECchr774246695Missense_Mutationrs782112033R134Q0.43
UCECchr7742544015'UTRnovel0.4

Copy Number Variations (CNVs)
CancerTypeFreq Q-value
DLBCAMP0.27080.13215
TGCTAMP0.70670.035574
THCADEL0.0020.27619

Survival Analysis
CancerP-value Q-value
KIRC0.0012

Kaplan-Meier Survival Analysis

MESO0.00019

Kaplan-Meier Survival Analysis

ACC0.00011

Kaplan-Meier Survival Analysis

UCS0.017

Kaplan-Meier Survival Analysis

LUSC0.036

Kaplan-Meier Survival Analysis

KIRP0.047

Kaplan-Meier Survival Analysis

CESC0.01

Kaplan-Meier Survival Analysis

LAML0.022

Kaplan-Meier Survival Analysis

KICH0.011

Kaplan-Meier Survival Analysis

UCEC0.011

Kaplan-Meier Survival Analysis

GBM0.0035

Kaplan-Meier Survival Analysis

LIHC0.00047

Kaplan-Meier Survival Analysis

DLBC0.025

Kaplan-Meier Survival Analysis

THCA0.027

Kaplan-Meier Survival Analysis

LUAD0.0012

Kaplan-Meier Survival Analysis

UVM0.0001

Kaplan-Meier Survival Analysis

OV0.0066

Kaplan-Meier Survival Analysis

Drugs

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Eesembl ID



Cell lines and drugs in GSE70138 or GSE92742

  • Description
  • RBPome
  • Literatures
  • Expression
  • Transcripts
  • Gene Model
  • Pathways
  • PPI
  • Orthologs
  • Gene Ontology
Description
Ensembl ID
ENSG00000049541 (Gene tree)
Gene ID
5982
Gene Symbol
RFC2
Alias
A1|RFC40
Full Name
replication factor C subunit 2
Gene Type
protein_coding
Species
Homo_sapiens
Status
confidence
Strand
Minus strand
Length
22,974 bases
Position
chr7:74,231,485-74,254,458
Accession
9970
RBP type
non-canonical RBP
Summary
This gene encodes a member of the activator 1 small subunits family. The elongation of primed DNA templates by DNA polymerase delta and epsilon requires the action of the accessory proteins, proliferating cell nuclear antigen (PCNA) and replication factor C (RFC). Replication factor C, also called activator 1, is a protein complex consisting of five distinct subunits. This gene encodes the 40 kD subunit, which has been shown to be responsible for binding ATP and may help promote cell survival. Disruption of this gene is associated with Williams syndrome. Alternatively spliced transcript variants encoding distinct isoforms have been described. A pseudogene of this gene has been defined on chromosome 2. [provided by RefSeq, Jul 2013]
RNA binding proteome (RBPome)
PIDTitleMethod TimeAuthorDoi
29431736Capturing the interactome of newly transcribed RNAPolyT-RICK & Hela2018 Feb 12Bao XDOI: 10.1038/nmeth.4595
29431736Capturing the interactome of newly transcribed RNARICK & Hela2018 Feb 12Bao XDOI: 10.1038/nmeth.4595

Literatures on RNA binding capacity
PIDTitleArticle TimeAuthorDoi
8812460Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients.Genomics1996 Sep 1Osborne LR-
19144639Structural basis of the influenza A virus RNA polymerase PB2 RNA-binding domain containing the pathogenicity-determinant lysine 627 residue.J Biol Chem2009 Mar 13Kuzuhara Tdoi: 10.1074/jbc.C800224200
Expression
Transcripts
Transcript IDNameLengthRefSeq ID Protein IDLengthRefSeq IDUniportKB ID
ENST00000485545RFC2-208847-ENSP00000419320120 (aa)-H7C596
ENST00000055077RFC2-2011695-ENSP00000055077354 (aa)-P35250
ENST00000463194RFC2-203853-ENSP00000419827101 (aa)-H7C5G4
ENST00000497430RFC2-212753-ENSP00000420404198 (aa)-H7C5P4
ENST00000479105RFC2-206957-ENSP0000042039252 (aa)-H7C5P1
ENST00000480432RFC2-207871-ENSP0000041889977 (aa)-F8WC37
ENST00000352131RFC2-2021576-ENSP00000275627320 (aa)-P35250
ENST00000470266RFC2-204881-ENSP0000042051375 (aa)-H7C5Q7
ENST00000621097RFC2-2131635XM_006716080ENSP00000479768251 (aa)XP_006716143A0A087WVY3
ENST00000473493RFC2-205304--- (aa)--
ENST00000493156RFC2-210782-ENSP0000042056337 (aa)-F8WDC9
ENST00000494019RFC2-211730-ENSP0000041934187 (aa)-H7C5A0
ENST00000491206RFC2-209726-ENSP0000042073128 (aa)-H7C5S7
Gene Model
Click here to download ENSG00000049541's gene model file
Pathways
Pathway IDPathway NameSource
hsa03030DNA replicationKEGG
hsa03420Nucleotide excision repairKEGG
hsa03430Mismatch repairKEGG
Protein-Protein Interaction (PPI)

Clik here to download ENSG00000049541's network

* RBP PPI network refers to all genes directly bind to RBP
Orthologs identified by RBPome
Ensembl IDGene SymbolCoverageIdentiy OrthologGene SymbolCoverageIdentiy Species
ENSG00000049541RFC29896.356ENSMUSG00000023104Rfc210091.243Mus_musculus
ENSG00000049541RFC29461.506YOL094C9661.218Saccharomyces_cerevisiae
Gene Ontology
Go IDGo_termPubmedIDEvidenceCategory
GO:0003689DNA clamp loader activity21873635.IBAFunction
GO:0003689DNA clamp loader activity12930902.IDAFunction
GO:0005515protein binding9488738.15655353.18499658.IPIFunction
GO:0005524ATP binding-IEAFunction
GO:0005634nucleus21873635.IBAComponent
GO:0005654nucleoplasm-TASComponent
GO:0005663DNA replication factor C complex21873635.IBAComponent
GO:0005663DNA replication factor C complex9488738.IDAComponent
GO:0006260DNA replication-TASProcess
GO:0006261DNA-dependent DNA replication21873635.IBAProcess
GO:0006283transcription-coupled nucleotide-excision repair-TASProcess
GO:0006296nucleotide-excision repair, DNA incision, 5'-to lesion-TASProcess
GO:0006297nucleotide-excision repair, DNA gap filling-TASProcess
GO:0019899enzyme binding-IEAFunction
GO:0019985translesion synthesis-TASProcess
GO:0031390Ctf18 RFC-like complex12930902.IDAComponent
GO:0032201telomere maintenance via semi-conservative replication-TASProcess
GO:0033683nucleotide-excision repair, DNA incision-TASProcess
GO:0042276error-prone translesion synthesis-TASProcess
GO:0042769DNA damage response, detection of DNA damage-TASProcess
GO:0043142single-stranded DNA-dependent ATPase activity12930902.IDAFunction
GO:0070987error-free translesion synthesis-TASProcess
GO:1900264positive regulation of DNA-directed DNA polymerase activity12930902.IDAProcess
GO:1901796regulation of signal transduction by p53 class mediator-TASProcess
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