Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101927950 (uncharacterized LOC101927950)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927950
Atlas_Id 67253
Location 6p25.1  [Link to chromosome band 6p25]
Location_base_pair Starts at 5664986 and ends at 5695272 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)LOC101927950  101927950  uncharacterized LOC101927950
Aliases
GeneCards (Weizmann)LOC101927950
Ensembl hg19 (Hinxton)ENSG00000270174 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000270174 [Gene_View]  ENSG00000270174 [Sequence]  chr6:5664986-5695272 [Contig_View]  LOC101927950 [Vega]
ICGC DataPortalENSG00000270174
TCGA cBioPortalLOC101927950
AceView (NCBI)LOC101927950
Genatlas (Paris)LOC101927950
WikiGenes101927950
SOURCE (Princeton)LOC101927950
Genetics Home Reference (NIH)LOC101927950
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927950  -     chr6:5664986-5695272 -  6p25.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927950  -     6p25.1   [Description]    (hg19-Feb_2009)
EnsemblLOC101927950 - 6p25.1 [CytoView hg19]  LOC101927950 - 6p25.1 [CytoView hg38]
Mapping of homologs : NCBILOC101927950 [Mapview hg19]  LOC101927950 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC080548
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927950
Cluster EST : UnigeneHs.571136 [ NCBI ]
CGAP (NCI)Hs.571136
Alternative Splicing GalleryENSG00000270174
Gene ExpressionLOC101927950 [ NCBI-GEO ]   LOC101927950 [ EBI - ARRAY_EXPRESS ]   LOC101927950 [ SEEK ]   LOC101927950 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927950 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927950
GTEX Portal (Tissue expression)LOC101927950
Human Protein AtlasENSG00000270174-LOC101927950 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927950
DMDM Disease mutations101927950
Blocks (Seattle)LOC101927950
Human Protein Atlas [tissue]ENSG00000270174-LOC101927950 [tissue]
Protein Interaction databases
FunCoupENSG00000270174
BioGRIDLOC101927950
STRING (EMBL)LOC101927950
ZODIACLOC101927950
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927950
BioCentury BCIQLOC101927950
ClinGenLOC101927950
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927950
Clinical trialLOC101927950
Miscellaneous
canSAR (ICR)LOC101927950 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927950
EVEXLOC101927950
GoPubMedLOC101927950
iHOPLOC101927950
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Jul 30 14:02:51 CEST 2018

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