Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101928847 (uncharacterized LOC101928847)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928847
Atlas_Id 67443
Location 11q23.2  [Link to chromosome band 11q23]
Location_base_pair Starts at 112959280 and ends at 112963460 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)

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)LOC101928847  101928847  uncharacterized LOC101928847
Aliases
GeneCards (Weizmann)LOC101928847
Ensembl hg19 (Hinxton)ENSG00000247416 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000247416 [Gene_View]  chr11:112959280-112963460 [Contig_View]  LOC101928847 [Vega]
ICGC DataPortalENSG00000247416
TCGA cBioPortalLOC101928847
AceView (NCBI)LOC101928847
Genatlas (Paris)LOC101928847
WikiGenes101928847
SOURCE (Princeton)LOC101928847
Genetics Home Reference (NIH)LOC101928847
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101928847  -     chr11:112959280-112963460 -  11q23.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101928847  -     11q23.2   [Description]    (hg19-Feb_2009)
EnsemblLOC101928847 - 11q23.2 [CytoView hg19]  LOC101928847 - 11q23.2 [CytoView hg38]
Mapping of homologs : NCBILOC101928847 [Mapview hg19]  LOC101928847 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AL833634
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101928847
Cluster EST : UnigeneHs.711235 [ NCBI ]
CGAP (NCI)Hs.711235
Alternative Splicing GalleryENSG00000247416
Gene ExpressionLOC101928847 [ NCBI-GEO ]   LOC101928847 [ EBI - ARRAY_EXPRESS ]   LOC101928847 [ SEEK ]   LOC101928847 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928847 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928847
GTEX Portal (Tissue expression)LOC101928847
Human Protein AtlasENSG00000247416-LOC101928847 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928847
DMDM Disease mutations101928847
Blocks (Seattle)LOC101928847
Human Protein Atlas [tissue]ENSG00000247416-LOC101928847 [tissue]
Protein Interaction databases
FunCoupENSG00000247416
BioGRIDLOC101928847
STRING (EMBL)LOC101928847
ZODIACLOC101928847
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928847
BioCentury BCIQLOC101928847
ClinGenLOC101928847
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928847
Clinical trialLOC101928847
Miscellaneous
canSAR (ICR)LOC101928847 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101928847
EVEXLOC101928847
GoPubMedLOC101928847
iHOPLOC101928847
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 : Tue Nov 21 13:51:35 CET 2017

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