Atlas of Genetics and Cytogenetics in Oncology and Haematology


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PAGE4 (PAGE family member 4)

Identity

Alias_namesGAGEC1
G antigen, family C, 1
P antigen family, member 4 (prostate associated)
Alias_symbol (synonym)PAGE-4
CT16.7
Other aliasGAGE-9
JM-27
JM27
PAGE-1
HGNC (Hugo) PAGE4
LocusID (NCBI) 9506
Atlas_Id 43007
Location Xp11.23  [Link to chromosome band Xp11]
Location_base_pair Starts at 49593863 and ends at 49598867 bp from pter ( according to hg19-Feb_2009)
Fusion genes
(updated 2016)
PSD3 (8p22) / PAGE4 (Xp11.23)PSD3 8p22 / PAGE4 Xp11.23

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)PAGE4   4108
Cards
Entrez_Gene (NCBI)PAGE4  9506  PAGE family member 4
AliasesCT16.7; GAGE-9; GAGEC1; JM-27; 
JM27; PAGE-1; PAGE-4
GeneCards (Weizmann)PAGE4
Ensembl hg19 (Hinxton)ENSG00000101951 [Gene_View]  chrX:49593863-49598867 [Contig_View]  PAGE4 [Vega]
Ensembl hg38 (Hinxton)ENSG00000101951 [Gene_View]  chrX:49593863-49598867 [Contig_View]  PAGE4 [Vega]
ICGC DataPortalENSG00000101951
TCGA cBioPortalPAGE4
AceView (NCBI)PAGE4
Genatlas (Paris)PAGE4
WikiGenes9506
SOURCE (Princeton)PAGE4
Genetics Home Reference (NIH)PAGE4
Genomic and cartography
GoldenPath hg19 (UCSC)PAGE4  -     chrX:49593863-49598867 +  Xp11.23   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)PAGE4  -     Xp11.23   [Description]    (hg38-Dec_2013)
EnsemblPAGE4 - Xp11.23 [CytoView hg19]  PAGE4 - Xp11.23 [CytoView hg38]
Mapping of homologs : NCBIPAGE4 [Mapview hg19]  PAGE4 [Mapview hg38]
OMIM300287   
Gene and transcription
Genbank (Entrez)AF275258 AI093155 AJ005894 AK092503 AK312039
RefSeq transcript (Entrez)NM_001318877 NM_007003
RefSeq genomic (Entrez)NC_000023 NC_018934 NT_079573 NW_004929440
Consensus coding sequences : CCDS (NCBI)PAGE4
Cluster EST : UnigeneHs.441038 [ NCBI ]
CGAP (NCI)Hs.441038
Alternative Splicing GalleryENSG00000101951
Gene ExpressionPAGE4 [ NCBI-GEO ]   PAGE4 [ EBI - ARRAY_EXPRESS ]   PAGE4 [ SEEK ]   PAGE4 [ MEM ]
Gene Expression Viewer (FireBrowse)PAGE4 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)9506
GTEX Portal (Tissue expression)PAGE4
Protein : pattern, domain, 3D structure
UniProt/SwissProtO60829   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtO60829  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProO60829
Splice isoforms : SwissVarO60829
PhosPhoSitePlusO60829
Domains : Interpro (EBI)GAGE    GAGE_fam   
Domain families : Pfam (Sanger)GAGE (PF05831)   
Domain families : Pfam (NCBI)pfam05831   
Conserved Domain (NCBI)PAGE4
DMDM Disease mutations9506
Blocks (Seattle)PAGE4
SuperfamilyO60829
Human Protein AtlasENSG00000101951
Peptide AtlasO60829
HPRD02239
IPIIPI00299244   
Protein Interaction databases
DIP (DOE-UCLA)O60829
IntAct (EBI)O60829
FunCoupENSG00000101951
BioGRIDPAGE4
STRING (EMBL)PAGE4
ZODIACPAGE4
Ontologies - Pathways
QuickGOO60829
Ontology : AmiGOmolecular_function  cellular_component  biological_process  
Ontology : EGO-EBImolecular_function  cellular_component  biological_process  
NDEx NetworkPAGE4
Atlas of Cancer Signalling NetworkPAGE4
Wikipedia pathwaysPAGE4
Orthology - Evolution
OrthoDB9506
GeneTree (enSembl)ENSG00000101951
Phylogenetic Trees/Animal Genes : TreeFamPAGE4
HOVERGENO60829
HOGENOMO60829
Homologs : HomoloGenePAGE4
Homology/Alignments : Family Browser (UCSC)PAGE4
Gene fusions - Rearrangements
Fusion : MitelmanPSD3/PAGE4 [8p22/Xp11.23]  [t(X;8)(p11;p22)]  
Fusion: TCGAPSD3 8p22 PAGE4 Xp11.23 BRCA
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerPAGE4 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)PAGE4
dbVarPAGE4
ClinVarPAGE4
1000_GenomesPAGE4 
Exome Variant ServerPAGE4
ExAC (Exome Aggregation Consortium)PAGE4 (select the gene name)
Genetic variants : HAPMAP9506
Genomic Variants (DGV)PAGE4 [DGVbeta]
DECIPHER (Syndromes)X:49593863-49598867  ENSG00000101951
CONAN: Copy Number AnalysisPAGE4 
Mutations
ICGC Data PortalPAGE4 
TCGA Data PortalPAGE4 
Broad Tumor PortalPAGE4
OASIS PortalPAGE4 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICPAGE4  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDPAGE4
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch PAGE4
DgiDB (Drug Gene Interaction Database)PAGE4
DoCM (Curated mutations)PAGE4 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)PAGE4 (select a term)
intoGenPAGE4
Cancer3DPAGE4(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM300287   
Orphanet
MedgenPAGE4
Genetic Testing Registry PAGE4
NextProtO60829 [Medical]
TSGene9506
GENETestsPAGE4
Huge Navigator PAGE4 [HugePedia]
snp3D : Map Gene to Disease9506
BioCentury BCIQPAGE4
ClinGenPAGE4
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD9506
Chemical/Pharm GKB GenePA28523
Clinical trialPAGE4
Miscellaneous
canSAR (ICR)PAGE4 (select the gene name)
Probes
Litterature
PubMed13 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMinePAGE4
EVEXPAGE4
GoPubMedPAGE4
iHOPPAGE4
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Thu Mar 30 15:13:26 CEST 2017

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