Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101928737 (uncharacterized LOC101928737)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928737
Atlas_Id 67417
Location 16q24.2  [Link to chromosome band 16q24]
Location_base_pair Starts at 87494187 and ends at 87515630 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)LOC101928737  101928737  uncharacterized LOC101928737
Aliases
GeneCards (Weizmann)LOC101928737
Ensembl hg19 (Hinxton)ENSG00000260750 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000260750 [Gene_View]  chr16:87494187-87515630 [Contig_View]  LOC101928737 [Vega]
ICGC DataPortalENSG00000260750
TCGA cBioPortalLOC101928737
AceView (NCBI)LOC101928737
Genatlas (Paris)LOC101928737
WikiGenes101928737
SOURCE (Princeton)LOC101928737
Genetics Home Reference (NIH)LOC101928737
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101928737  -     chr16:87494187-87515630 +  16q24.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101928737  -     16q24.2   [Description]    (hg19-Feb_2009)
EnsemblLOC101928737 - 16q24.2 [CytoView hg19]  LOC101928737 - 16q24.2 [CytoView hg38]
Mapping of homologs : NCBILOC101928737 [Mapview hg19]  LOC101928737 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC131758
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101928737
Cluster EST : UnigeneHs.579009 [ NCBI ]
CGAP (NCI)Hs.579009
Alternative Splicing GalleryENSG00000260750
Gene ExpressionLOC101928737 [ NCBI-GEO ]   LOC101928737 [ EBI - ARRAY_EXPRESS ]   LOC101928737 [ SEEK ]   LOC101928737 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928737 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928737
GTEX Portal (Tissue expression)LOC101928737
Human Protein AtlasENSG00000260750-LOC101928737 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928737
DMDM Disease mutations101928737
Blocks (Seattle)LOC101928737
Human Protein Atlas [tissue]ENSG00000260750-LOC101928737 [tissue]
Protein Interaction databases
FunCoupENSG00000260750
BioGRIDLOC101928737
STRING (EMBL)LOC101928737
ZODIACLOC101928737
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928737
BioCentury BCIQLOC101928737
ClinGenLOC101928737
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928737
Clinical trialLOC101928737
Miscellaneous
canSAR (ICR)LOC101928737 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101928737
EVEXLOC101928737
GoPubMedLOC101928737
iHOPLOC101928737
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 12:04:39 CET 2017

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