Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101929452 (uncharacterized LOC101929452)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929452
Atlas_Id 67559
Location 2p25.1  [Link to chromosome band 2p25]
Location_base_pair Starts at 7062727 and ends at 7077880 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)LOC101929452  101929452  uncharacterized LOC101929452
Aliases
GeneCards (Weizmann)LOC101929452
Ensembl hg19 (Hinxton)ENSG00000223884 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000223884 [Gene_View]  chr2:7062727-7077880 [Contig_View]  LOC101929452 [Vega]
ICGC DataPortalENSG00000223884
TCGA cBioPortalLOC101929452
AceView (NCBI)LOC101929452
Genatlas (Paris)LOC101929452
WikiGenes101929452
SOURCE (Princeton)LOC101929452
Genetics Home Reference (NIH)LOC101929452
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929452  -     chr2:7062727-7077880 -  2p25.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929452  -     2p25.1   [Description]    (hg19-Feb_2009)
EnsemblLOC101929452 - 2p25.1 [CytoView hg19]  LOC101929452 - 2p25.1 [CytoView hg38]
Mapping of homologs : NCBILOC101929452 [Mapview hg19]  LOC101929452 [Mapview hg38]
Gene and transcription
Genbank (Entrez)DB071295 DB084532
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929452
Alternative Splicing GalleryENSG00000223884
Gene ExpressionLOC101929452 [ NCBI-GEO ]   LOC101929452 [ EBI - ARRAY_EXPRESS ]   LOC101929452 [ SEEK ]   LOC101929452 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929452 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929452
GTEX Portal (Tissue expression)LOC101929452
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929452
DMDM Disease mutations101929452
Blocks (Seattle)LOC101929452
Human Protein AtlasENSG00000223884
Protein Interaction databases
FunCoupENSG00000223884
BioGRIDLOC101929452
STRING (EMBL)LOC101929452
ZODIACLOC101929452
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929452
BioCentury BCIQLOC101929452
ClinGenLOC101929452
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929452
Clinical trialLOC101929452
Miscellaneous
canSAR (ICR)LOC101929452 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929452
EVEXLOC101929452
GoPubMedLOC101929452
iHOPLOC101929452
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 : Wed Jun 7 16:06:23 CEST 2017

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