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LOC105369332 (uncharacterized LOC105369332)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 105369332
Atlas_Id 78305
Location 11q12.3  [Link to chromosome band 11q12]
Location_base_pair Starts at 62832234 and ends at 62834041 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)LOC105369332  105369332  uncharacterized LOC105369332
Aliases
GeneCards (Weizmann)LOC105369332
Ensembl hg19 (Hinxton)ENSG00000256690 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000256690 [Gene_View]  chr11:62832234-62834041 [Contig_View]  LOC105369332 [Vega]
ICGC DataPortalENSG00000256690
TCGA cBioPortalLOC105369332
AceView (NCBI)LOC105369332
Genatlas (Paris)LOC105369332
WikiGenes105369332
SOURCE (Princeton)LOC105369332
Genetics Home Reference (NIH)LOC105369332
Genomic and cartography
GoldenPath hg38 (UCSC)LOC105369332  -     chr11:62832234-62834041 +  11q12.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC105369332  -     11q12.3   [Description]    (hg19-Feb_2009)
EnsemblLOC105369332 - 11q12.3 [CytoView hg19]  LOC105369332 - 11q12.3 [CytoView hg38]
Mapping of homologs : NCBILOC105369332 [Mapview hg19]  LOC105369332 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC105369332
Alternative Splicing GalleryENSG00000256690
Gene ExpressionLOC105369332 [ NCBI-GEO ]   LOC105369332 [ EBI - ARRAY_EXPRESS ]   LOC105369332 [ SEEK ]   LOC105369332 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC105369332 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)105369332
GTEX Portal (Tissue expression)LOC105369332
Human Protein AtlasENSG00000256690-LOC105369332 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC105369332
DMDM Disease mutations105369332
Blocks (Seattle)LOC105369332
Human Protein Atlas [tissue]ENSG00000256690-LOC105369332 [tissue]
Protein Interaction databases
FunCoupENSG00000256690
BioGRIDLOC105369332
STRING (EMBL)LOC105369332
ZODIACLOC105369332
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease105369332
BioCentury BCIQLOC105369332
ClinGenLOC105369332
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD105369332
Clinical trialLOC105369332
Miscellaneous
canSAR (ICR)LOC105369332 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC105369332
EVEXLOC105369332
GoPubMedLOC105369332
iHOPLOC105369332
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 12:06:35 CET 2017

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