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LOC100421746 (PAGE family member 5 pseudogene)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100421746
Atlas_Id 76812
Location Xp11.21  [Link to chromosome band Xp11]
Location_base_pair Starts at 55280088 and ends at 55288786 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)-   -
Cards
Entrez_Gene (NCBI)LOC100421746  100421746  PAGE family member 5 pseudogene
Aliases
GeneCards (Weizmann)LOC100421746
Ensembl hg19 (Hinxton)ENSG00000232765 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000232765 [Gene_View]  chrX:55280088-55288786 [Contig_View]  LOC100421746 [Vega]
ICGC DataPortalENSG00000232765
TCGA cBioPortalLOC100421746
AceView (NCBI)LOC100421746
Genatlas (Paris)LOC100421746
WikiGenes100421746
SOURCE (Princeton)LOC100421746
Genetics Home Reference (NIH)LOC100421746
Genomic and cartography
GoldenPath hg38 (UCSC)LOC100421746  -     chrX:55280088-55288786 +  Xp11.21   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC100421746  -     Xp11.21   [Description]    (hg19-Feb_2009)
EnsemblLOC100421746 - Xp11.21 [CytoView hg19]  LOC100421746 - Xp11.21 [CytoView hg38]
Mapping of homologs : NCBILOC100421746 [Mapview hg19]  LOC100421746 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AA437034 AI651025
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC100421746
Cluster EST : UnigeneHs.662612 [ NCBI ]
CGAP (NCI)Hs.662612
Alternative Splicing GalleryENSG00000232765
Gene ExpressionLOC100421746 [ NCBI-GEO ]   LOC100421746 [ EBI - ARRAY_EXPRESS ]   LOC100421746 [ SEEK ]   LOC100421746 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100421746 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100421746
GTEX Portal (Tissue expression)LOC100421746
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100421746
DMDM Disease mutations100421746
Blocks (Seattle)LOC100421746
Human Protein AtlasENSG00000232765
Protein Interaction databases
FunCoupENSG00000232765
BioGRIDLOC100421746
STRING (EMBL)LOC100421746
ZODIACLOC100421746
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100421746
BioCentury BCIQLOC100421746
ClinGenLOC100421746
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100421746
Clinical trialLOC100421746
Miscellaneous
canSAR (ICR)LOC100421746 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100421746
EVEXLOC100421746
GoPubMedLOC100421746
iHOPLOC100421746
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Mon Sep 18 13:18:34 CEST 2017

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