Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101928659 (uncharacterized LOC101928659)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928659
Atlas_Id 78300
Location 16q24.2  [Link to chromosome band 16q24]
Location_base_pair Starts at 87317509 and ends at 87318043 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)LOC101928659  101928659  uncharacterized LOC101928659
Aliases
GeneCards (Weizmann)LOC101928659
Ensembl hg19 (Hinxton)ENSG00000270006 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000270006 [Gene_View]  chr16:87317509-87318043 [Contig_View]  LOC101928659 [Vega]
ICGC DataPortalENSG00000270006
TCGA cBioPortalLOC101928659
AceView (NCBI)LOC101928659
Genatlas (Paris)LOC101928659
WikiGenes101928659
SOURCE (Princeton)LOC101928659
Genetics Home Reference (NIH)LOC101928659
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101928659  -     chr16:87317509-87318043 +  16q24.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101928659  -     16q24.2   [Description]    (hg19-Feb_2009)
EnsemblLOC101928659 - 16q24.2 [CytoView hg19]  LOC101928659 - 16q24.2 [CytoView hg38]
Mapping of homologs : NCBILOC101928659 [Mapview hg19]  LOC101928659 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BQ640484
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101928659
Cluster EST : UnigeneHs.667450 [ NCBI ]
CGAP (NCI)Hs.667450
Alternative Splicing GalleryENSG00000270006
Gene ExpressionLOC101928659 [ NCBI-GEO ]   LOC101928659 [ EBI - ARRAY_EXPRESS ]   LOC101928659 [ SEEK ]   LOC101928659 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928659 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928659
GTEX Portal (Tissue expression)LOC101928659
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928659
DMDM Disease mutations101928659
Blocks (Seattle)LOC101928659
Human Protein AtlasENSG00000270006
Protein Interaction databases
FunCoupENSG00000270006
BioGRIDLOC101928659
STRING (EMBL)LOC101928659
ZODIACLOC101928659
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928659
BioCentury BCIQLOC101928659
ClinGenLOC101928659
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928659
Clinical trialLOC101928659
Miscellaneous
canSAR (ICR)LOC101928659 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101928659
EVEXLOC101928659
GoPubMedLOC101928659
iHOPLOC101928659
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 16:05:34 CEST 2017

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