Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101927657 (uncharacterized LOC101927657)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927657
Atlas_Id 67190
Location 8q24.21  [Link to chromosome band 8q24]
Location_base_pair Starts at 126325495 and ends at 126329533 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)LOC101927657  101927657  uncharacterized LOC101927657
Aliases
GeneCards (Weizmann)LOC101927657
Ensembl hg19 (Hinxton)ENSG00000244791 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000244791 [Gene_View]  chr8:126325495-126329533 [Contig_View]  LOC101927657 [Vega]
ICGC DataPortalENSG00000244791
TCGA cBioPortalLOC101927657
AceView (NCBI)LOC101927657
Genatlas (Paris)LOC101927657
WikiGenes101927657
SOURCE (Princeton)LOC101927657
Genetics Home Reference (NIH)LOC101927657
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927657  -     chr8:126325495-126329533 +  8q24.21   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927657  -     8q24.21   [Description]    (hg19-Feb_2009)
EnsemblLOC101927657 - 8q24.21 [CytoView hg19]  LOC101927657 - 8q24.21 [CytoView hg38]
Mapping of homologs : NCBILOC101927657 [Mapview hg19]  LOC101927657 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC038572
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927657
Cluster EST : UnigeneHs.552133 [ NCBI ]
CGAP (NCI)Hs.552133
Alternative Splicing GalleryENSG00000244791
Gene ExpressionLOC101927657 [ NCBI-GEO ]   LOC101927657 [ EBI - ARRAY_EXPRESS ]   LOC101927657 [ SEEK ]   LOC101927657 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927657 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927657
GTEX Portal (Tissue expression)LOC101927657
Human Protein AtlasENSG00000244791-LOC101927657 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927657
DMDM Disease mutations101927657
Blocks (Seattle)LOC101927657
Human Protein Atlas [tissue]ENSG00000244791-LOC101927657 [tissue]
Protein Interaction databases
FunCoupENSG00000244791
BioGRIDLOC101927657
STRING (EMBL)LOC101927657
ZODIACLOC101927657
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927657
BioCentury BCIQLOC101927657
ClinGenLOC101927657
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927657
Clinical trialLOC101927657
Miscellaneous
canSAR (ICR)LOC101927657 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927657
EVEXLOC101927657
GoPubMedLOC101927657
iHOPLOC101927657
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 13:50:20 CET 2017

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