Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101928896 (uncharacterized LOC101928896)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928896
Atlas_Id 67458
Location 11q14.1  [Link to chromosome band 11q14]
Location_base_pair Starts at 78533176 and ends at 78558565 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)LOC101928896  101928896  uncharacterized LOC101928896
Aliases
GeneCards (Weizmann)LOC101928896
Ensembl hg19 (Hinxton)ENSG00000255084 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000255084 [Gene_View]  chr11:78533176-78558565 [Contig_View]  LOC101928896 [Vega]
ICGC DataPortalENSG00000255084
TCGA cBioPortalLOC101928896
AceView (NCBI)LOC101928896
Genatlas (Paris)LOC101928896
WikiGenes101928896
SOURCE (Princeton)LOC101928896
Genetics Home Reference (NIH)LOC101928896
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101928896  -     chr11:78533176-78558565 +  11q14.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101928896  -     11q14.1   [Description]    (hg19-Feb_2009)
EnsemblLOC101928896 - 11q14.1 [CytoView hg19]  LOC101928896 - 11q14.1 [CytoView hg38]
Mapping of homologs : NCBILOC101928896 [Mapview hg19]  LOC101928896 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AI201276 BC042472
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101928896
Cluster EST : UnigeneHs.659055 [ NCBI ]
CGAP (NCI)Hs.659055
Alternative Splicing GalleryENSG00000255084
Gene ExpressionLOC101928896 [ NCBI-GEO ]   LOC101928896 [ EBI - ARRAY_EXPRESS ]   LOC101928896 [ SEEK ]   LOC101928896 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928896 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928896
GTEX Portal (Tissue expression)LOC101928896
Human Protein AtlasENSG00000255084-LOC101928896 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928896
DMDM Disease mutations101928896
Blocks (Seattle)LOC101928896
Human Protein Atlas [tissue]ENSG00000255084-LOC101928896 [tissue]
Protein Interaction databases
FunCoupENSG00000255084
BioGRIDLOC101928896
STRING (EMBL)LOC101928896
ZODIACLOC101928896
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928896
BioCentury BCIQLOC101928896
ClinGenLOC101928896
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928896
Clinical trialLOC101928896
Miscellaneous
canSAR (ICR)LOC101928896 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101928896
EVEXLOC101928896
GoPubMedLOC101928896
iHOPLOC101928896
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 12:04:49 CET 2017

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