Browse ORC1 in pancancer

Summary
SymbolORC1
Nameorigin recognition complex subunit 1
Aliases HSORC1; PARC1; origin recognition complex, subunit 1, S. cerevisiae, homolog-like; origin recognition comple ......
Location1p32.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Cancer Gene Databases ONGene (Oncogene) , TSGene (Tumor suppressor gene) , NCG (Network of Cancer Genes)
Content > Domain, Function and Classification
> Gene Ontology
> KEGG and Reactome Pathway
> Domain, Function and Classification
 
Domain PF00004 ATPase family associated with various cellular activities (AAA)
PF01426 BAH domain
PF09079 CDC6
Function

Component of the origin recognition complex (ORC) that binds origins of replication. DNA-binding is ATP-dependent. The DNA sequences that define origins of replication have not been identified yet. ORC is required to assemble the pre-replication complex necessary to initiate DNA replication.

Classification
Class Modification Substrate Product PubMed
# # # # #
> Gene Ontology
 
Biological Process GO:0000082 G1/S transition of mitotic cell cycle
GO:0000083 regulation of transcription involved in G1/S transition of mitotic cell cycle
GO:0006260 DNA replication
GO:0006261 DNA-dependent DNA replication
GO:0006270 DNA replication initiation
GO:0044770 cell cycle phase transition
GO:0044772 mitotic cell cycle phase transition
GO:0044843 cell cycle G1/S phase transition
Molecular Function GO:0003682 chromatin binding
Cellular Component GO:0000781 chromosome, telomeric region
GO:0000784 nuclear chromosome, telomeric region
GO:0000808 origin recognition complex
GO:0005664 nuclear origin of replication recognition complex
GO:0044454 nuclear chromosome part
GO:0098687 chromosomal region
> KEGG and Reactome Pathway
 
KEGG hsa04110 Cell cycle
Reactome R-HSA-176187: Activation of ATR in response to replication stress
R-HSA-68962: Activation of the pre-replicative complex
R-HSA-68616: Assembly of the ORC complex at the origin of replication
R-HSA-68867: Assembly of the pre-replicative complex
R-HSA-69298: Association of licensing factors with the pre-replicative complex
R-HSA-68689: CDC6 association with the ORC
R-HSA-68827: CDT1 association with the CDC6
R-HSA-1640170: Cell Cycle
R-HSA-69620: Cell Cycle Checkpoints
R-HSA-69278: Cell Cycle, Mitotic
R-HSA-69306: DNA Replication
R-HSA-69002: DNA Replication Pre-Initiation
R-HSA-113510: E2F mediated regulation of DNA replication
R-HSA-113507: E2F-enabled inhibition of pre-replication complex formation
R-HSA-69206: G1/S Transition
R-HSA-69205: G1/S-Specific Transcription
R-HSA-69481: G2/M Checkpoints
R-HSA-68874: M/G1 Transition
R-HSA-453279: Mitotic G1-G1/S phases
R-HSA-68949: Orc1 removal from chromatin
R-HSA-69304: Regulation of DNA replication
R-HSA-69300: Removal of licensing factors from origins
R-HSA-69242: S Phase
R-HSA-69052: Switching of origins to a post-replicative state
R-HSA-69239: Synthesis of DNA
Summary
SymbolORC1
Nameorigin recognition complex subunit 1
Aliases HSORC1; PARC1; origin recognition complex, subunit 1, S. cerevisiae, homolog-like; origin recognition comple ......
Location1p32.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Cancer Gene Databases ONGene (Oncogene) , TSGene (Tumor suppressor gene) , NCG (Network of Cancer Genes)
Content > Mutation landscape in primary tumor tissue from TCGA
> Mutation landscape in cancer cell line from CCLE
> All mutations from COSMIC database V81
> Variations from text mining
> The Cancer Genome Atlas (TCGA)
 
> Cancer Cell Line Encyclopedia (CCLE)
 
There is no record.
> Catalogue of Somatic Mutations in Cancer (COSMIC)
 
COSMIC ID CDS change AA change Mutation Type Anatomical Site
COSM3490662c.1399C>Tp.P467SSubstitution - MissenseSkin
COSM4710322c.253C>Tp.R85*Substitution - NonsenseLarge_intestine
COSM4516587c.2072_2073GG>AAp.R691KSubstitution - MissenseSkin
COSM3490661c.1515C>Tp.P505PSubstitution - coding silentSkin
COSM4975985c.924G>Cp.K308NSubstitution - MissenseOesophagus
COSM5812351c.1925A>Tp.H642LSubstitution - MissenseLiver
COSM219977c.2360G>Ap.R787QSubstitution - MissenseProstate
COSM2192899c.649T>Cp.S217PSubstitution - MissenseLarge_intestine
COSM1218899c.1822C>Tp.R608*Substitution - NonsenseLarge_intestine
COSM464743c.1476A>Tp.R492RSubstitution - coding silentKidney
COSM4797694c.605G>Ap.W202*Substitution - NonsenseLiver
COSM1737358c.437C>Tp.T146MSubstitution - MissenseCentral_nervous_system
COSM1602532c.256G>Cp.V86LSubstitution - MissenseLiver
COSM1218897c.269T>Cp.V90ASubstitution - MissenseLarge_intestine
COSM1320998c.2531G>Ap.R844QSubstitution - MissenseOvary
COSM2192866c.2517C>Tp.N839NSubstitution - coding silentLarge_intestine
COSM5456469c.1755+6C>Tp.?UnknownLarge_intestine
COSM4144075c.2400T>Cp.S800SSubstitution - coding silentThyroid
COSM910656c.961C>Tp.R321*Substitution - NonsenseSkin
COSM1343379c.354G>Ap.P118PSubstitution - coding silentLarge_intestine
COSM5962073c.2308T>Cp.S770PSubstitution - MissenseBreast
COSM1218900c.613G>Ap.A205TSubstitution - MissenseLarge_intestine
COSM5821533c.1187+1G>Tp.?UnknownLiver
COSM397115c.144G>Cp.Q48HSubstitution - MissenseLung
COSM5716863c.396T>Gp.L132LSubstitution - coding silentSkin
COSM291200c.698C>Ap.A233DSubstitution - MissenseLarge_intestine
COSM3985128c.1866C>Tp.L622LSubstitution - coding silentKidney
COSM910652c.1429C>Tp.R477*Substitution - NonsenseEndometrium
COSM681800c.1319C>Tp.S440FSubstitution - MissenseLung
COSM233026c.433C>Tp.P145SSubstitution - MissenseSkin
COSM1637054c.1781C>Gp.A594GSubstitution - MissenseBone
COSM4456528c.1012C>Tp.P338SSubstitution - MissenseSkin
COSM4623071c.1604T>Cp.V535ASubstitution - MissenseLarge_intestine
COSM3934775c.216C>Tp.F72FSubstitution - coding silentOesophagus
COSM4710320c.1110T>Cp.N370NSubstitution - coding silentLarge_intestine
COSM3360954c.1957G>Ap.A653TSubstitution - MissenseKidney
COSM4617574c.608C>Tp.T203ISubstitution - MissenseUpper_aerodigestive_tract
COSM5716863c.396T>Gp.L132LSubstitution - coding silentSkin
COSM1197041c.934C>Tp.P312SSubstitution - MissenseLung
COSM464742c.1769A>Gp.Q590RSubstitution - MissenseKidney
COSM4008808c.2422A>Cp.M808LSubstitution - MissenseStomach
COSM910648c.1863+2T>Cp.?UnknownEndometrium
COSM1738456c.2324A>Gp.Q775RSubstitution - MissenseHaematopoietic_and_lymphoid_tissue
COSM4547465c.423G>Ap.K141KSubstitution - coding silentSkin
COSM4397587c.1132C>Tp.R378CSubstitution - MissenseSkin
COSM459063c.495C>Tp.F165FSubstitution - coding silentCervix
COSM5716863c.396T>Gp.L132LSubstitution - coding silentSkin
COSM910649c.1656G>Ap.Q552QSubstitution - coding silentEndometrium
COSM910647c.2030G>Ap.C677YSubstitution - MissenseEndometrium
COSM125073c.1552G>Ap.V518MSubstitution - MissenseUpper_aerodigestive_tract
COSM3360953c.2100T>Cp.F700FSubstitution - coding silentKidney
COSM414859c.224-1G>Ap.?UnknownUrinary_tract
COSM273061c.1331G>Ap.R444QSubstitution - MissenseLarge_intestine
COSM4008812c.790C>Tp.R264WSubstitution - MissenseStomach
COSM5053580c.2295G>Ap.T765TSubstitution - coding silentStomach
COSM681798c.216C>Ap.F72LSubstitution - MissenseLung
COSM5518162c.567C>Tp.P189PSubstitution - coding silentBiliary_tract
COSM1218899c.1822C>Tp.R608*Substitution - NonsenseStomach
COSM5969466c.1506G>Cp.E502DSubstitution - MissenseUpper_aerodigestive_tract
COSM4144074c.2402A>Gp.Q801RSubstitution - MissenseThyroid
COSM4008814c.434C>Tp.P145LSubstitution - MissenseStomach
COSM910650c.1496C>Tp.A499VSubstitution - MissenseEndometrium
COSM426440c.712G>Cp.E238QSubstitution - MissenseBreast
COSM681799c.944G>Ap.R315HSubstitution - MissenseLung
COSM4820382c.1221G>Ap.E407ESubstitution - coding silentCervix
COSM910657c.956G>Tp.R319ISubstitution - MissenseEndometrium
COSM3805543c.1430G>Ap.R477QSubstitution - MissenseBreast
COSM3790117c.444G>Ap.L148LSubstitution - coding silentUrinary_tract
COSM464741c.1936C>Tp.R646WSubstitution - MissenseLarge_intestine
COSM910653c.1402C>Tp.R468CSubstitution - MissenseEndometrium
COSM4167694c.1999G>Ap.V667MSubstitution - MissenseHaematopoietic_and_lymphoid_tissue
COSM1165525c.1132C>Ap.R378SSubstitution - MissenseLarge_intestine
COSM1343374c.1364C>Tp.T455MSubstitution - MissenseLarge_intestine
COSM5588542c.1997G>Tp.R666LSubstitution - MissenseSkin
COSM267086c.1669G>Tp.A557SSubstitution - MissenseLarge_intestine
COSM5957235c.289G>Tp.A97SSubstitution - MissenseThyroid
COSM910656c.961C>Tp.R321*Substitution - NonsenseEndometrium
COSM3490658c.1920C>Tp.P640PSubstitution - coding silentSkin
COSM3386229c.2489G>Ap.R830HSubstitution - MissensePancreas
COSM3490663c.1137C>Tp.I379ISubstitution - coding silentSkin
COSM3934774c.807G>Ap.S269SSubstitution - coding silentOesophagus
COSM4888664c.2138C>Ap.A713ESubstitution - MissenseUpper_aerodigestive_tract
COSM3805542c.1690C>Gp.Q564ESubstitution - MissenseBreast
COSM910658c.943C>Tp.R315CSubstitution - MissenseEndometrium
COSM4008810c.2111C>Tp.A704VSubstitution - MissenseStomach
COSM1343375c.1187+2T>Cp.?UnknownLarge_intestine
COSM241017c.2128A>Gp.R710GSubstitution - MissenseProstate
COSM4825032c.841G>Cp.D281HSubstitution - MissenseCervix
COSM3751283c.1115C>Tp.A372VSubstitution - MissenseLarge_intestine
COSM369111c.400C>Tp.R134WSubstitution - MissenseLung
COSM4008809c.2381C>Tp.T794MSubstitution - MissenseStomach
COSM3805545c.528G>Tp.L176FSubstitution - MissenseBreast
COSM2192883c.1646G>Ap.R549HSubstitution - MissenseLarge_intestine
COSM2192906c.448A>Cp.N150HSubstitution - MissenseLarge_intestine
COSM3490660c.1596C>Tp.I532ISubstitution - coding silentSkin
COSM1343373c.1491T>Ap.V497VSubstitution - coding silentLarge_intestine
COSM5719123c.1584G>Tp.G528GSubstitution - coding silentSkin
COSM4559124c.792G>Ap.R264RSubstitution - coding silentSkin
COSM146512c.1636G>Cp.E546QSubstitution - MissenseStomach
COSM5044088c.2078G>Ap.R693QSubstitution - MissenseLiver
COSM3805544c.1107G>Tp.Q369HSubstitution - MissenseBreast
COSM1492066c.2161C>Tp.R721WSubstitution - MissenseKidney
COSM384697c.1790C>Tp.A597VSubstitution - MissenseLung
COSM3711660c.208G>Ap.E70KSubstitution - MissenseUpper_aerodigestive_tract
COSM4819342c.1704C>Gp.V568VSubstitution - coding silentCervix
COSM3386230c.1265A>Gp.D422GSubstitution - MissensePancreas
COSM5462440c.2023A>Gp.R675GSubstitution - MissenseLarge_intestine
COSM673788c.2470T>Ap.S824TSubstitution - MissenseEndometrium
COSM5353371c.1864C>Tp.L622FSubstitution - MissenseLarge_intestine
COSM4528327c.1527G>Ap.Q509QSubstitution - coding silentSkin
COSM5962905c.130G>Ap.E44KSubstitution - MissenseBreast
COSM3711660c.208G>Ap.E70KSubstitution - MissenseUpper_aerodigestive_tract
COSM4144073c.2405A>Cp.H802PSubstitution - MissenseThyroid
COSM5431698c.2292C>Gp.I764MSubstitution - MissenseOesophagus
COSM4710321c.429G>Tp.V143VSubstitution - coding silentLarge_intestine
COSM910659c.522G>Ap.A174ASubstitution - coding silentEndometrium
COSM5479523c.1414C>Gp.P472ASubstitution - MissenseLarge_intestine
COSM4617574c.608C>Tp.T203ISubstitution - MissenseLarge_intestine
COSM4165242c.757T>Ap.C253SSubstitution - MissenseKidney
COSM4008813c.602C>Tp.S201FSubstitution - MissenseStomach
COSM4135625c.1684C>Tp.P562SSubstitution - MissensePancreas
COSM5005050c.1998G>Ap.R666RSubstitution - coding silentHaematopoietic_and_lymphoid_tissue
COSM5963750c.1756-1G>Ap.?UnknownBreast
COSM3667697c.808G>Ap.E270KSubstitution - MissenseLiver
COSM163194c.1192C>Gp.L398VSubstitution - MissenseBreast
COSM2192909c.377C>Tp.A126VSubstitution - MissenseLarge_intestine
COSM1602532c.256G>Cp.V86LSubstitution - MissenseLiver
COSM2192891c.1266C>Tp.D422DSubstitution - coding silentLarge_intestine
COSM5430672c.519_523delTGCGGp.F173fs*4Deletion - FrameshiftOesophagus
COSM4808242c.322G>Ap.G108SSubstitution - MissensePancreas
COSM4565775c.2526_2527CC>TTp.L843FSubstitution - MissenseSkin
COSM5483908c.1560C>Tp.S520SSubstitution - coding silentLarge_intestine
COSM4772224c.1475G>Tp.R492LSubstitution - MissenseStomach
COSM1260672c.1777A>Gp.T593ASubstitution - MissenseOesophagus
COSM4755336c.1006C>Tp.L336FSubstitution - MissenseStomach
COSM4008807c.2509A>Gp.S837GSubstitution - MissenseStomach
COSM5812481c.1253A>Tp.D418VSubstitution - MissenseLiver
COSM910655c.1001G>Tp.R334ISubstitution - MissenseEndometrium
COSM4746225c.917A>Gp.D306GSubstitution - MissenseCentral_nervous_system
COSM5478839c.1709G>Tp.G570VSubstitution - MissenseLarge_intestine
COSM5381200c.217G>Ap.E73KSubstitution - MissenseSkin
COSM3490659c.1826G>Ap.G609ESubstitution - MissenseSkin
COSM1343372c.1867G>Ap.D623NSubstitution - MissenseLarge_intestine
COSM4936562c.752C>Ap.T251NSubstitution - MissenseLiver
COSM1687684c.58C>Gp.P20ASubstitution - MissenseSkin
COSM3934775c.216C>Tp.F72FSubstitution - coding silentSkin
COSM4400068c.184A>Cp.N62HSubstitution - MissenseSkin
COSM369111c.400C>Tp.R134WSubstitution - MissenseLarge_intestine
COSM1218898c.1553T>Cp.V518ASubstitution - MissenseLarge_intestine
COSM72032c.951C>Gp.I317MSubstitution - MissenseOvary
COSM910654c.1160C>Ap.T387NSubstitution - MissenseEndometrium
COSM4755337c.982A>Gp.I328VSubstitution - MissenseStomach
COSM4008811c.1483C>Tp.L495LSubstitution - coding silentStomach
COSM338257c.2086C>Ap.H696NSubstitution - MissenseLung
COSM910651c.1439C>Ap.A480DSubstitution - MissenseEndometrium
COSM4797694c.605G>Ap.W202*Substitution - NonsenseLiver
COSM4144076c.2399G>Tp.S800ISubstitution - MissenseThyroid
COSM459064c.509C>Tp.S170LSubstitution - MissenseCervix
COSM5499565c.1560C>Ap.S520RSubstitution - MissenseBiliary_tract
COSM2192910c.365G>Ap.S122NSubstitution - MissenseLarge_intestine
COSM2192895c.886delAp.T296fs*21Deletion - FrameshiftLarge_intestine
COSM3490657c.2153A>Gp.D718GSubstitution - MissenseSkin
COSM3490664c.451G>Ap.E151KSubstitution - MissenseSkin
COSM143462c.1501_1502CC>TTp.P501FSubstitution - MissenseSkin
COSM5621432c.652G>Ap.A218TSubstitution - MissenseHaematopoietic_and_lymphoid_tissue
COSM4452210c.1673A>Gp.N558SSubstitution - MissenseSkin
COSM5954288c.353C>Tp.P118LSubstitution - MissenseUpper_aerodigestive_tract
COSM1197041c.934C>Tp.P312SSubstitution - MissenseLung
COSM5917331c.863C>Tp.P288LSubstitution - MissenseSkin
COSM5699002c.2380A>Tp.T794SSubstitution - MissenseSoft_tissue
COSM2192910c.365G>Ap.S122NSubstitution - MissenseLarge_intestine
> Text Mining based Variations
 
There is no record for ORC1.
Summary
SymbolORC1
Nameorigin recognition complex subunit 1
Aliases HSORC1; PARC1; origin recognition complex, subunit 1, S. cerevisiae, homolog-like; origin recognition comple ......
Location1p32.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Cancer Gene Databases ONGene (Oncogene) , TSGene (Tumor suppressor gene) , NCG (Network of Cancer Genes)
Content > Post-translational modification (PTM)
> Post-translational modification (PTM)
 
 Filter By:
Uniprot ID Position Amino Acid Description Upstream Enzyme Affected By Mutation Amino Acid Sequence Variant
Q13415203TPhosphothreonine-NoNone detected
Q13415252SPhosphoserine-NoNone detected
Q13415255SPhosphoserine-NoNone detected
Q13415273SPhosphoserine-NoNone detected
Q13415287SPhosphoserine-NoNone detected
Q13415326KN6-acetyllysine-NoNone detected
Q13415337TPhosphothreonine-NoNone detected
Q13415340SPhosphoserine-NoNone detected
Q13415417SPhosphoserine-NoNone detected
Q13415420SPhosphoserine-NoNone detected
Q13415478SPhosphoserine-NoNone detected
Summary
SymbolORC1
Nameorigin recognition complex subunit 1
Aliases HSORC1; PARC1; origin recognition complex, subunit 1, S. cerevisiae, homolog-like; origin recognition comple ......
Location1p32.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Cancer Gene Databases ONGene (Oncogene) , TSGene (Tumor suppressor gene) , NCG (Network of Cancer Genes)
Content > Expression analysis in primary tumor tissue from TCGA
> Expression level in cancer cell line from CCLE
> Expression level in human normal tissue from HPA
> Text mining based expression change
> The Cancer Genome Atlas (TCGA)
 


  Differential expression analysis for cancers with more than 10 normal samples
Cancer Full Name # N # T Median (N) Median (T) LogFC Adj. P Status
BLCABladder urothelial carcinoma194080.5383.4012.7134.44e-19Over
BRCABreast invasive carcinoma1121100-0.0422.3552.3861.59e-63Over
CESCCervical and endocervical cancers3306-0.5074.648NANANA
COADColon adenocarcinoma414592.9614.0381.0215.82e-15Over
ESCAEsophageal carcinoma11185-0.7793.7463.8075.3e-24Over
GBMGlioblastoma multiforme5166-1.7732.705NANANA
HNSCHead and Neck squamous cell carcinoma445222.6353.7581.7247.32e-30Over
KIRCKidney renal clear cell carcinoma72534-0.4990.7381.2281.59e-18Over
KIRPKidney renal papillary cell carcinoma32291-0.1110.6610.9424.53e-06Over
LAMLAcute Myeloid Leukemia0173NA4.888NANANA
LGGBrain Lower Grade Glioma0530NA-0.022NANANA
LIHCLiver hepatocellular carcinoma50373-2.2271.2973.2581.39e-38Over
LUADLung adenocarcinoma59517-0.5482.5192.8616.92e-48Over
LUSCLung squamous cell carcinoma51501-0.2723.8643.9961.7e-120Over
OVOvarian serous cystadenocarcinoma0307NA3.219NANANA
PAADPancreatic adenocarcinoma41790.7571.215NANANA
PCPGPheochromocytoma and Paraganglioma3184-0.537-0.839NANANA
PRADProstate adenocarcinoma52498-0.559-0.1010.5814.54e-05Over
READRectum adenocarcinoma101672.8813.9360.880.00353Over
SARCSarcoma22630.3722.936NANANA
SKCMSkin Cutaneous Melanoma14723.2963.192NANANA
STADStomach adenocarcinoma354152.143.4992.392.05e-21Over
TGCTTesticular Germ Cell Tumors0156NA5.106NANANA
THCAThyroid carcinoma59509-1.076-0.0050.7361.75e-07Over
THYMThymoma21203.7764.07NANANA
UCECUterine Corpus Endometrial Carcinoma35546-0.7353.1083.4969.58e-61Over
> Cancer Cell Line Encyclopedia (CCLE)
 

There is no record.
> The Human Protein Atlas (HPA)
 


Tissue Expression Level (TPM)
Adipose tissue 0.5
Adrenal gland 0.6
Appendix 4.9
Bone marrow 18
Breast 1.3
Cerebral cortex 0.6
Cervix, uterine 0.5
Colon 3.4
Duodenum 1.7
Endometrium 1
Epididymis 0.2
Esophagus 2.3
Fallopian tube 0.5
Gallbladder 0.7
Heart muscle 0
Kidney 0.5
Liver 0.3
Lung 0.7
Lymph node 8
Ovary 0.3
Pancreas 0
Parathyroid gland 0.6
Placenta 2.7
Prostate 0.5
Rectum 4.6
Salivary gland 0.1
Seminal vesicle 0.3
Skeletal muscle 0
Skin 2.4
Small intestine 2.6
Smooth muscle 1.3
Spleen 1.7
Stomach 1
Testis 6.9
Thyroid gland 0.4
Tonsil 7.2
Urinary bladder 1.5
> Text Mining based Expression
 
There is no record.
Summary
SymbolORC1
Nameorigin recognition complex subunit 1
Aliases HSORC1; PARC1; origin recognition complex, subunit 1, S. cerevisiae, homolog-like; origin recognition comple ......
Location1p32.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Cancer Gene Databases ONGene (Oncogene) , TSGene (Tumor suppressor gene) , NCG (Network of Cancer Genes)
Content > Somatic copy number alteration in primary tomur tissue
> The Cancer Genome Atlas (TCGA)
 


  Correlation between expression and SCNA as well as percentage of patients in different status.
Cancer Full Name # Sample R P % Loss % Neutral % Gain Status
BLCABladder urothelial carcinoma4040.241.1e-0613.466.120.5Neutral
BRCABreast invasive carcinoma10750.341.38e-3028.357.514.2Neutral
CESCCervical and endocervical cancers2920.3554.45e-105.563.730.8Neutral
COADColon adenocarcinoma4490.3343.42e-1326.169.94Neutral
ESCAEsophageal carcinoma1830.1310.077828.457.913.7Neutral
GBMGlioblastoma multiforme1470.2560.001746.178.215.6Neutral
HNSCHead and Neck squamous cell carcinoma5140.1871.99e-0513.673.512.8Neutral
KIRCKidney renal clear cell carcinoma5250.2992.82e-1213.9833Neutral
KIRPKidney renal papillary cell carcinoma2880.2693.7e-0612.885.81.4Neutral
LAMLAcute Myeloid Leukemia1660.0930.233097.62.4Neutral
LGGBrain Lower Grade Glioma5130.4514.73e-2736.560.82.7Loss
LIHCLiver hepatocellular carcinoma3640.2662.5e-0726.662.610.7Neutral
LUADLung adenocarcinoma5120.1757.16e-0520.954.724.4Neutral
LUSCLung squamous cell carcinoma4980.1758.62e-0536.548.415.1Loss
OVOvarian serous cystadenocarcinoma3000.3665.77e-1115.749.335Gain
PAADPancreatic adenocarcinoma1770.2090.0052124.370.65.1Neutral
PCPGPheochromocytoma and Paraganglioma1620.3922.53e-0771.628.40Loss
PRADProstate adenocarcinoma4910.1150.011111.2880.8Neutral
READRectum adenocarcinoma1640.2560.00094132.363.44.3Neutral
SARCSarcoma2550.4767.91e-1611.458.430.2Neutral
SKCMSkin Cutaneous Melanoma3670.4074.63e-1616.662.121.3Neutral
STADStomach adenocarcinoma4130.1370.0054218.973.18Neutral
TGCTTesticular Germ Cell Tumors1500.3861.06e-0617.358.724Neutral
THCAThyroid carcinoma4970.0310.4890.898.60.6Neutral
THYMThymoma1190.1630.07635.993.30.8Neutral
UCECUterine Corpus Endometrial Carcinoma5370.1520.0004235.68410.4Neutral
Summary
SymbolORC1
Nameorigin recognition complex subunit 1
Aliases HSORC1; PARC1; origin recognition complex, subunit 1, S. cerevisiae, homolog-like; origin recognition comple ......
Location1p32.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Cancer Gene Databases ONGene (Oncogene) , TSGene (Tumor suppressor gene) , NCG (Network of Cancer Genes)
Content > Methylation level in the promoter region of CR
> Methylation level in the promoter region of CR
 


  Correlation between expression and methylation as well as differential methylation analysis.
Cancer Full Name R P # N # T Delta beta (T vs N) P value (T vs N) Status
BLCABladder urothelial carcinoma-0.1490.002117408-0.0220.000262NS/NA
BRCABreast invasive carcinoma-0.1080.001488378500.0391NS/NA
CESCCervical and endocervical cancers-0.0990.0813306NANANS/NA
COADColon adenocarcinoma-0.1410.012519297-0.0120.073NS/NA
ESCAEsophageal carcinoma-0.2080.003749185NANANS/NA
GBMGlioblastoma multiforme-0.2710.0293164NANANS/NA
HNSCHead and Neck squamous cell carcinoma-0.1050.014120522-0.0140.107NS/NA
KIRCKidney renal clear cell carcinoma-0.0360.50624319-0.0090.0114NS/NA
KIRPKidney renal papillary cell carcinoma-0.1950.00075123275-0.0060.203NS/NA
LAMLAcute Myeloid Leukemia-0.170.02660170NANANS/NA
LGGBrain Lower Grade Glioma-0.3462.55e-160530NANANS/NA
LIHCLiver hepatocellular carcinoma-0.2654.8e-0841373-0.0922.63e-33NS/NA
LUADLung adenocarcinoma-0.2123.07e-0621456-0.0260.000127NS/NA
LUSCLung squamous cell carcinoma-0.2441.75e-068370NANANS/NA
OVOvarian serous cystadenocarcinoma-0.10.8109NANANS/NA
PAADPancreatic adenocarcinoma-0.0330.6594179NANANS/NA
PCPGPheochromocytoma and Paraganglioma-0.1710.01963184NANANS/NA
PRADProstate adenocarcinoma-0.2373.33e-0835498-0.0231.42e-08NS/NA
READRectum adenocarcinoma-0.1970.0482299NANANS/NA
SARCSarcoma-0.3211.18e-070263NANANS/NA
SKCMSkin Cutaneous Melanoma-0.0860.06241471NANANS/NA
STADStomach adenocarcinoma-0.1840.0003610372NANANS/NA
TGCTTesticular Germ Cell Tumors-0.2150.007160156NANANS/NA
THCAThyroid carcinoma-0.090.033150509-0.0020.0493NS/NA
THYMThymoma-0.0090.9182120NANANS/NA
UCECUterine Corpus Endometrial Carcinoma-0.1350.0035834431-0.0280.00028NS/NA
Summary
SymbolORC1
Nameorigin recognition complex subunit 1
Aliases HSORC1; PARC1; origin recognition complex, subunit 1, S. cerevisiae, homolog-like; origin recognition comple ......
Location1p32.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Cancer Gene Databases ONGene (Oncogene) , TSGene (Tumor suppressor gene) , NCG (Network of Cancer Genes)
Content > Primary tumor tissue from TCGA
> Normal tumor tissue from HPA
>The Cancer Genome Atlas (TCGA)
 
There is no record.
> The Human Protein Atlas (HPA)
 


Tissue Level Level Name
Adrenal gland 2 Medium
Appendix 1 Low
Bone marrow 1 Low
Breast 1 Low
Bronchus 2 Medium
Caudate 2 Medium
Cerebellum 3 High
Cerebral cortex 3 High
Cervix, uterine 1 Low
Colon 2 Medium
Duodenum 1 Low
Endometrium 0 Not detected
Epididymis 2 Medium
Esophagus 2 Medium
Fallopian tube 1 Low
Gallbladder 2 Medium
Heart muscle 1 Low
Hippocampus 2 Medium
Kidney 1 Low
Liver 2 Medium
Lung 1 Low
Lymph node 1 Low
Nasopharynx 2 Medium
Oral mucosa 1 Low
Ovary 1 Low
Pancreas 3 High
Parathyroid gland 3 High
Placenta 2 Medium
Prostate 1 Low
Rectum 2 Medium
Salivary gland 0 Not detected
Seminal vesicle 1 Low
Skeletal muscle 2 Medium
Skin 2 Medium
Small intestine 1 Low
Smooth muscle 1 Low
Soft tissue 2 Medium
Spleen 0 Not detected
Stomach 1 Low
Testis 3 High
Thyroid gland 2 Medium
Tonsil 2 Medium
Urinary bladder 1 Low
Vagina 2 Medium
Summary
SymbolORC1
Nameorigin recognition complex subunit 1
Aliases HSORC1; PARC1; origin recognition complex, subunit 1, S. cerevisiae, homolog-like; origin recognition comple ......
Location1p32.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Cancer Gene Databases ONGene (Oncogene) , TSGene (Tumor suppressor gene) , NCG (Network of Cancer Genes)
Content > Association between expresson and subtype
> Overall survival analysis based on expression
> Association between expresson and stage
> Association between expresson and grade
> Subtype
 


  Association between expresson and subtype.
Cancer Full Name # Patients P Value (Kruskal-Wallis) Association Source
BLCABladder urothelial carcinoma1280.0413Significant24476821
BRCABreast invasive carcinoma5212.06e-56Significant23000897
COADColon adenocarcinoma1490.142NS22810696
GBMGlioblastoma multiforme1570.000177Significant26824661
HNSCHead and Neck squamous cell carcinoma2790.00227Significant25631445
KIRPKidney renal papillary cell carcinoma1610.00733Significant26536169
LGGBrain Lower Grade Glioma5134.15e-25Significant26824661
LUADLung adenocarcinoma2301.83e-20Significant25079552
LUSCLung squamous cell carcinoma1782.29e-07Significant22960745
OVOvarian serous cystadenocarcinoma2874.51e-08Significant21720365
PRADProstate adenocarcinoma3330.34NS26544944
READRectum adenocarcinoma670.385NS22810696
SKCMSkin Cutaneous Melanoma3150.0068Significant26091043
STADStomach adenocarcinoma2777.62e-16Significant25079317
THCAThyroid carcinoma3911.89e-11Significant25417114
UCECUterine Corpus Endometrial Carcinoma2323.02e-14Significant23636398
> Overall survival
 

  Overall survival analysis based on expression.
Cancer Full Name # Patients Hazard Ratio P Value (Log Rank Test) Association
BLCABladder urothelial carcinoma405 1.2460.288NS
BRCABreast invasive carcinoma1079 1.1410.552NS
CESCCervical and endocervical cancers291 0.5860.103NS
COADColon adenocarcinoma439 0.6210.117NS
ESCAEsophageal carcinoma184 1.1930.6NS
GBMGlioblastoma multiforme158 0.8060.383NS
HNSCHead and Neck squamous cell carcinoma518 0.6690.0501NS
KIRCKidney renal clear cell carcinoma531 1.8320.00343Shorter
KIRPKidney renal papillary cell carcinoma287 3.7470.00116Shorter
LAMLAcute Myeloid Leukemia149 1.5760.116NS
LGGBrain Lower Grade Glioma511 3.7635.47e-07Shorter
LIHCLiver hepatocellular carcinoma365 2.040.00378Shorter
LUADLung adenocarcinoma502 1.6860.014Shorter
LUSCLung squamous cell carcinoma494 0.7410.111NS
OVOvarian serous cystadenocarcinoma303 0.9040.631NS
PAADPancreatic adenocarcinoma177 2.5340.00347Shorter
PCPGPheochromocytoma and Paraganglioma179 0.9690.982NS
PRADProstate adenocarcinoma497 3.0190.315NS
READRectum adenocarcinoma159 0.3890.129NS
SARCSarcoma259 2.2230.00779Shorter
SKCMSkin Cutaneous Melanoma459 1.8240.00184Shorter
STADStomach adenocarcinoma388 0.6740.0802NS
TGCTTesticular Germ Cell Tumors134 577026061.8960.325NS
THCAThyroid carcinoma500 1.1560.849NS
THYMThymoma119 0.1320.0427Longer
UCECUterine Corpus Endometrial Carcinoma543 1.6780.134NS
> Stage
 

  Association between expresson and stage.
Cancer Full Name # Patients R Value (Spearman) P Value (Spearman) Association
BLCABladder urothelial carcinoma406 0.0660.184NS
BRCABreast invasive carcinoma1071 0.0330.285NS
CESCCervical and endocervical cancers167 0.0320.682NS
COADColon adenocarcinoma445 -0.150.00146Lower
ESCAEsophageal carcinoma162 -0.0410.601NS
HNSCHead and Neck squamous cell carcinoma448 -0.0030.945NS
KIRCKidney renal clear cell carcinoma531 0.1480.000601Higher
KIRPKidney renal papillary cell carcinoma260 0.3563.44e-09Higher
LIHCLiver hepatocellular carcinoma347 0.1750.00106Higher
LUADLung adenocarcinoma507 0.1748.41e-05Higher
LUSCLung squamous cell carcinoma497 0.0210.644NS
OVOvarian serous cystadenocarcinoma302 -0.110.0568NS
PAADPancreatic adenocarcinoma176 0.1090.15NS
READRectum adenocarcinoma156 -0.0970.228NS
SKCMSkin Cutaneous Melanoma410 -0.0940.0566NS
STADStomach adenocarcinoma392 -0.0460.364NS
TGCTTesticular Germ Cell Tumors81 0.3160.00412Higher
THCAThyroid carcinoma499 0.0350.442NS
UCECUterine Corpus Endometrial Carcinoma501 0.1360.00233Higher
> Grade
 

  Association between expresson and grade.
Cancer Full Name # Patients R Value (Spearman) P Value (Spearman) Association
CESCCervical and endocervical cancers272 0.0240.693NS
HNSCHead and Neck squamous cell carcinoma498 0.2387.24e-08Higher
KIRCKidney renal clear cell carcinoma525 0.1852.08e-05Higher
LGGBrain Lower Grade Glioma514 0.3886.47e-20Higher
LIHCLiver hepatocellular carcinoma366 0.3232.53e-10Higher
OVOvarian serous cystadenocarcinoma296 0.0680.242NS
PAADPancreatic adenocarcinoma176 0.2190.00357Higher
STADStomach adenocarcinoma406 -0.1010.0416Lower
UCECUterine Corpus Endometrial Carcinoma534 0.4621.41e-29Higher
Summary
SymbolORC1
Nameorigin recognition complex subunit 1
Aliases HSORC1; PARC1; origin recognition complex, subunit 1, S. cerevisiae, homolog-like; origin recognition comple ......
Location1p32.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Cancer Gene Databases ONGene (Oncogene) , TSGene (Tumor suppressor gene) , NCG (Network of Cancer Genes)
Content > Targets inferred by reverse engineering method
> Targets identified by ChIP-seq data
> Targets inferred by reverse engineering method
 
> Targets identified by ChIP-seq data
 
Summary
SymbolORC1
Nameorigin recognition complex subunit 1
Aliases HSORC1; PARC1; origin recognition complex, subunit 1, S. cerevisiae, homolog-like; origin recognition comple ......
Location1p32.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Cancer Gene Databases ONGene (Oncogene) , TSGene (Tumor suppressor gene) , NCG (Network of Cancer Genes)
Content > Drugs from DrugBank database
> Drugs from DrugBank database
 
There is no record for ORC1.
Summary
SymbolORC1
Nameorigin recognition complex subunit 1
Aliases HSORC1; PARC1; origin recognition complex, subunit 1, S. cerevisiae, homolog-like; origin recognition comple ......
Location1p32.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Cancer Gene Databases ONGene (Oncogene) , TSGene (Tumor suppressor gene) , NCG (Network of Cancer Genes)
Content > Protein-Protein Interaction Network
> miRNA Regulatory Relationship
> Interactions from Text Mining
> Protein-Protein Interaction Network
 
> miRNA Regulatory Relationship
 
There is no record for ORC1.
> Interactions from Text Mining
 
There is no record for ORC1.