Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101927989 (uncharacterized LOC101927989)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927989
Atlas_Id 78544
Location 18q23  [Link to chromosome band 18q23]
Location_base_pair Starts at 76491652 and ends at 76493915 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)LOC101927989  101927989  uncharacterized LOC101927989
Aliases
GeneCards (Weizmann)LOC101927989
Ensembl hg19 (Hinxton)ENSG00000265778 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000265778 [Gene_View]  chr18:76491652-76493915 [Contig_View]  LOC101927989 [Vega]
ICGC DataPortalENSG00000265778
TCGA cBioPortalLOC101927989
AceView (NCBI)LOC101927989
Genatlas (Paris)LOC101927989
WikiGenes101927989
SOURCE (Princeton)LOC101927989
Genetics Home Reference (NIH)LOC101927989
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927989  -     chr18:76491652-76493915 +  18q23   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927989  -     18q23   [Description]    (hg19-Feb_2009)
EnsemblLOC101927989 - 18q23 [CytoView hg19]  LOC101927989 - 18q23 [CytoView hg38]
Mapping of homologs : NCBILOC101927989 [Mapview hg19]  LOC101927989 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AW025577 BG329748
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927989
Cluster EST : UnigeneHs.665186 [ NCBI ]
CGAP (NCI)Hs.665186
Alternative Splicing GalleryENSG00000265778
Gene ExpressionLOC101927989 [ NCBI-GEO ]   LOC101927989 [ EBI - ARRAY_EXPRESS ]   LOC101927989 [ SEEK ]   LOC101927989 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927989 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927989
GTEX Portal (Tissue expression)LOC101927989
Human Protein AtlasENSG00000265778-LOC101927989 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927989
DMDM Disease mutations101927989
Blocks (Seattle)LOC101927989
Human Protein Atlas [tissue]ENSG00000265778-LOC101927989 [tissue]
Protein Interaction databases
FunCoupENSG00000265778
BioGRIDLOC101927989
STRING (EMBL)LOC101927989
ZODIACLOC101927989
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927989
BioCentury BCIQLOC101927989
ClinGenLOC101927989
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927989
Clinical trialLOC101927989
Miscellaneous
canSAR (ICR)LOC101927989 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927989
EVEXLOC101927989
GoPubMedLOC101927989
iHOPLOC101927989
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 12:03:51 CET 2017

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