Atlas of Genetics and Cytogenetics in Oncology and Haematology


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PAGE2 (PAGE family member 2)

Identity

Alias_namesGAGEC2
G antigen, family C, 2
P antigen family, member 2 (prostate associated)
Alias_symbol (synonym)MGC62094
PAGE-2
CT16.4
Other aliasGAGEE2
HGNC (Hugo) PAGE2
LocusID (NCBI) 203569
Atlas_Id 55575
Location Xp11.21  [Link to chromosome band Xp11]
Location_base_pair Starts at 55089052 and ends at 55092836 bp from pter ( according to hg38-Dec_2013)

Note

Non-annotated gene. Preliminary data : if you are an author
who wish to write a full paper/card on this gene, go to  How to contribute

DNA/RNA

 


External links

Nomenclature
HGNC (Hugo)PAGE2   31804
Cards
Entrez_Gene (NCBI)PAGE2  203569  PAGE family member 2
AliasesCT16.4; GAGEC2; GAGEE2; PAGE-2
GeneCards (Weizmann)PAGE2
Ensembl hg19 (Hinxton)ENSG00000234068 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000234068 [Gene_View]  chrX:55089052-55092836 [Contig_View]  PAGE2 [Vega]
ICGC DataPortalENSG00000234068
TCGA cBioPortalPAGE2
AceView (NCBI)PAGE2
Genatlas (Paris)PAGE2
WikiGenes203569
SOURCE (Princeton)PAGE2
Genetics Home Reference (NIH)PAGE2
Genomic and cartography
GoldenPath hg38 (UCSC)PAGE2  -     chrX:55089052-55092836 +  Xp11.21   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)PAGE2  -     Xp11.21   [Description]    (hg19-Feb_2009)
EnsemblPAGE2 - Xp11.21 [CytoView hg19]  PAGE2 - Xp11.21 [CytoView hg38]
Mapping of homologs : NCBIPAGE2 [Mapview hg19]  PAGE2 [Mapview hg38]
OMIM300738   
Gene and transcription
Genbank (Entrez)AA815378 BC054022 BX113994 HQ257927
RefSeq transcript (Entrez)NM_207339
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)PAGE2
Cluster EST : UnigeneHs.662489 [ NCBI ]
CGAP (NCI)Hs.662489
Alternative Splicing GalleryENSG00000234068
Gene ExpressionPAGE2 [ NCBI-GEO ]   PAGE2 [ EBI - ARRAY_EXPRESS ]   PAGE2 [ SEEK ]   PAGE2 [ MEM ]
Gene Expression Viewer (FireBrowse)PAGE2 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)203569
GTEX Portal (Tissue expression)PAGE2
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ7Z2X7   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ7Z2X7  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ7Z2X7
Splice isoforms : SwissVarQ7Z2X7
PhosPhoSitePlusQ7Z2X7
Domains : Interpro (EBI)GAGE    GAGE_fam   
Domain families : Pfam (Sanger)GAGE (PF05831)   
Domain families : Pfam (NCBI)pfam05831   
Domain families : Smart (EMBL)GAGE (SM01379)  
Conserved Domain (NCBI)PAGE2
DMDM Disease mutations203569
Blocks (Seattle)PAGE2
SuperfamilyQ7Z2X7
Human Protein AtlasENSG00000234068
Peptide AtlasQ7Z2X7
HPRD17565
IPIIPI00146451   IPI00647526   IPI00646044   
Protein Interaction databases
DIP (DOE-UCLA)Q7Z2X7
IntAct (EBI)Q7Z2X7
FunCoupENSG00000234068
BioGRIDPAGE2
STRING (EMBL)PAGE2
ZODIACPAGE2
Ontologies - Pathways
QuickGOQ7Z2X7
Ontology : AmiGOprotein binding  
Ontology : EGO-EBIprotein binding  
NDEx NetworkPAGE2
Atlas of Cancer Signalling NetworkPAGE2
Wikipedia pathwaysPAGE2
Orthology - Evolution
OrthoDB203569
GeneTree (enSembl)ENSG00000234068
Phylogenetic Trees/Animal Genes : TreeFamPAGE2
HOVERGENQ7Z2X7
HOGENOMQ7Z2X7
Homologs : HomoloGenePAGE2
Homology/Alignments : Family Browser (UCSC)PAGE2
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerPAGE2 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)PAGE2
dbVarPAGE2
ClinVarPAGE2
1000_GenomesPAGE2 
Exome Variant ServerPAGE2
ExAC (Exome Aggregation Consortium)PAGE2 (select the gene name)
Genetic variants : HAPMAP203569
Genomic Variants (DGV)PAGE2 [DGVbeta]
DECIPHERPAGE2 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisPAGE2 
Mutations
ICGC Data PortalPAGE2 
TCGA Data PortalPAGE2 
Broad Tumor PortalPAGE2
OASIS PortalPAGE2 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICPAGE2  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDPAGE2
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch PAGE2
DgiDB (Drug Gene Interaction Database)PAGE2
DoCM (Curated mutations)PAGE2 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)PAGE2 (select a term)
intoGenPAGE2
Cancer3DPAGE2(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM300738   
Orphanet
MedgenPAGE2
Genetic Testing Registry PAGE2
NextProtQ7Z2X7 [Medical]
TSGene203569
GENETestsPAGE2
Huge Navigator PAGE2 [HugePedia]
snp3D : Map Gene to Disease203569
BioCentury BCIQPAGE2
ClinGenPAGE2
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD203569
Chemical/Pharm GKB GenePA142671202
Clinical trialPAGE2
Miscellaneous
canSAR (ICR)PAGE2 (select the gene name)
Probes
Litterature
PubMed7 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMinePAGE2
EVEXPAGE2
GoPubMedPAGE2
iHOPPAGE2
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Fri May 19 12:30:06 CEST 2017

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