Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101927855 (uncharacterized LOC101927855)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927855
Atlas_Id 78501
Location 17q23.2  [Link to chromosome band 17q23]
Location_base_pair Starts at 61361668 and ends at 61367704 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)LOC101927855  101927855  uncharacterized LOC101927855
Aliases
GeneCards (Weizmann)LOC101927855
Ensembl hg19 (Hinxton)ENSG00000267131 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000267131 [Gene_View]  chr17:61361668-61367704 [Contig_View]  LOC101927855 [Vega]
ICGC DataPortalENSG00000267131
TCGA cBioPortalLOC101927855
AceView (NCBI)LOC101927855
Genatlas (Paris)LOC101927855
WikiGenes101927855
SOURCE (Princeton)LOC101927855
Genetics Home Reference (NIH)LOC101927855
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927855  -     chr17:61361668-61367704 -  17q23.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927855  -     17q23.2   [Description]    (hg19-Feb_2009)
EnsemblLOC101927855 - 17q23.2 [CytoView hg19]  LOC101927855 - 17q23.2 [CytoView hg38]
Mapping of homologs : NCBILOC101927855 [Mapview hg19]  LOC101927855 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BX115170
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927855
Cluster EST : UnigeneHs.662123 [ NCBI ]
CGAP (NCI)Hs.662123
Alternative Splicing GalleryENSG00000267131
Gene ExpressionLOC101927855 [ NCBI-GEO ]   LOC101927855 [ EBI - ARRAY_EXPRESS ]   LOC101927855 [ SEEK ]   LOC101927855 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927855 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927855
GTEX Portal (Tissue expression)LOC101927855
Human Protein AtlasENSG00000267131-LOC101927855 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927855
DMDM Disease mutations101927855
Blocks (Seattle)LOC101927855
Human Protein Atlas [tissue]ENSG00000267131-LOC101927855 [tissue]
Protein Interaction databases
FunCoupENSG00000267131
BioGRIDLOC101927855
STRING (EMBL)LOC101927855
ZODIACLOC101927855
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927855
BioCentury BCIQLOC101927855
ClinGenLOC101927855
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927855
Clinical trialLOC101927855
Miscellaneous
canSAR (ICR)LOC101927855 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927855
EVEXLOC101927855
GoPubMedLOC101927855
iHOPLOC101927855
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 : Thu Nov 9 12:03:42 CET 2017

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