Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101927759 (uncharacterized LOC101927759)

Identity

Alias (NCBI)-
HGNC (Hugo) -
LocusID (NCBI) 101927759
Atlas_Id 77864
Location 6p25.2  [Link to chromosome band 6p25]
Location_base_pair Starts at 3024063 and ends at 3027434 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)LOC101927759  101927759  uncharacterized LOC101927759
Aliases
GeneCards (Weizmann)LOC101927759
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]   [Sequence]  chr6:3024063-3027434 [Contig_View]  LOC101927759 [Vega]
TCGA cBioPortalLOC101927759
AceView (NCBI)LOC101927759
Genatlas (Paris)LOC101927759
WikiGenes101927759
SOURCE (Princeton)LOC101927759
Genetics Home Reference (NIH)LOC101927759
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927759  -     chr6:3024063-3027434 +  6p25.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927759  -     6p25.2   [Description]    (hg19-Feb_2009)
GoldenPathLOC101927759 - 6p25.2 [CytoView hg19]  LOC101927759 - 6p25.2 [CytoView hg38]
genome Data Viewer NCBILOC101927759 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AK097187
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927759
Gene ExpressionLOC101927759 [ NCBI-GEO ]   LOC101927759 [ EBI - ARRAY_EXPRESS ]   LOC101927759 [ SEEK ]   LOC101927759 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927759 [ Firebrowse - Broad ]
GenevisibleExpression of LOC101927759 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)101927759
GTEX Portal (Tissue expression)LOC101927759
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927759
DMDM Disease mutations101927759
Blocks (Seattle)LOC101927759
Protein Interaction databases
BioGRIDLOC101927759
STRING (EMBL)LOC101927759
ZODIACLOC101927759
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927759
BioCentury BCIQLOC101927759
ClinGenLOC101927759
Clinical trials, drugs, therapy
Protein Interactions : CTD101927759
Clinical trialLOC101927759
Miscellaneous
canSAR (ICR)LOC101927759 (select the gene name)
HarmonizomeLOC101927759
DataMed IndexLOC101927759
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927759
EVEXLOC101927759
GoPubMedLOC101927759
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 : Sat Aug 22 19:20:49 CEST 2020

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