Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101928708 (uncharacterized LOC101928708)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928708
Atlas_Id 67411
Location 16q24.2  [Link to chromosome band 16q24]
Location_base_pair Starts at 87212115 and ends at 87226429 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)LOC101928708  101928708  uncharacterized LOC101928708
Aliases
GeneCards (Weizmann)LOC101928708
Ensembl hg19 (Hinxton)ENSG00000261095 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000261095 [Gene_View]  chr16:87212115-87226429 [Contig_View]  LOC101928708 [Vega]
ICGC DataPortalENSG00000261095
TCGA cBioPortalLOC101928708
AceView (NCBI)LOC101928708
Genatlas (Paris)LOC101928708
WikiGenes101928708
SOURCE (Princeton)LOC101928708
Genetics Home Reference (NIH)LOC101928708
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101928708  -     chr16:87212115-87226429 +  16q24.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101928708  -     16q24.2   [Description]    (hg19-Feb_2009)
EnsemblLOC101928708 - 16q24.2 [CytoView hg19]  LOC101928708 - 16q24.2 [CytoView hg38]
Mapping of homologs : NCBILOC101928708 [Mapview hg19]  LOC101928708 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC043543
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101928708
Cluster EST : UnigeneHs.585717 [ NCBI ]
CGAP (NCI)Hs.585717
Alternative Splicing GalleryENSG00000261095
Gene ExpressionLOC101928708 [ NCBI-GEO ]   LOC101928708 [ EBI - ARRAY_EXPRESS ]   LOC101928708 [ SEEK ]   LOC101928708 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928708 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928708
GTEX Portal (Tissue expression)LOC101928708
Human Protein AtlasENSG00000261095-LOC101928708 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928708
DMDM Disease mutations101928708
Blocks (Seattle)LOC101928708
Human Protein Atlas [tissue]ENSG00000261095-LOC101928708 [tissue]
Protein Interaction databases
FunCoupENSG00000261095
BioGRIDLOC101928708
STRING (EMBL)LOC101928708
ZODIACLOC101928708
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928708
BioCentury BCIQLOC101928708
ClinGenLOC101928708
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928708
Clinical trialLOC101928708
Miscellaneous
canSAR (ICR)LOC101928708 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101928708
EVEXLOC101928708
GoPubMedLOC101928708
iHOPLOC101928708
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Thu Nov 9 12:04:36 CET 2017

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