Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101929089 (uncharacterized LOC101929089)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929089
Atlas_Id 67488
Location 11q23.3  [Link to chromosome band 11q23]
Location_base_pair Starts at 118519386 and ends at 118530775 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)LOC101929089  101929089  uncharacterized LOC101929089
Aliases
GeneCards (Weizmann)LOC101929089
Ensembl hg19 (Hinxton)ENSG00000255435 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000255435 [Gene_View]  chr11:118519386-118530775 [Contig_View]  LOC101929089 [Vega]
ICGC DataPortalENSG00000255435
TCGA cBioPortalLOC101929089
AceView (NCBI)LOC101929089
Genatlas (Paris)LOC101929089
WikiGenes101929089
SOURCE (Princeton)LOC101929089
Genetics Home Reference (NIH)LOC101929089
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929089  -     chr11:118519386-118530775 -  11q23.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929089  -     11q23.3   [Description]    (hg19-Feb_2009)
EnsemblLOC101929089 - 11q23.3 [CytoView hg19]  LOC101929089 - 11q23.3 [CytoView hg38]
Mapping of homologs : NCBILOC101929089 [Mapview hg19]  LOC101929089 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AI885123 AW449653 AW450539 AW611756 BE671460
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929089
Cluster EST : UnigeneHs.666633 [ NCBI ]
CGAP (NCI)Hs.666633
Alternative Splicing GalleryENSG00000255435
Gene ExpressionLOC101929089 [ NCBI-GEO ]   LOC101929089 [ EBI - ARRAY_EXPRESS ]   LOC101929089 [ SEEK ]   LOC101929089 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929089 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929089
GTEX Portal (Tissue expression)LOC101929089
Human Protein AtlasENSG00000255435-LOC101929089 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929089
DMDM Disease mutations101929089
Blocks (Seattle)LOC101929089
Human Protein Atlas [tissue]ENSG00000255435-LOC101929089 [tissue]
Protein Interaction databases
FunCoupENSG00000255435
BioGRIDLOC101929089
STRING (EMBL)LOC101929089
ZODIACLOC101929089
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929089
BioCentury BCIQLOC101929089
ClinGenLOC101929089
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929089
Clinical trialLOC101929089
Miscellaneous
canSAR (ICR)LOC101929089 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929089
EVEXLOC101929089
GoPubMedLOC101929089
iHOPLOC101929089
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 12:04:58 CET 2017

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