Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101927196 (uncharacterized LOC101927196)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927196
Atlas_Id 67080
Location 2q32.1  [Link to chromosome band 2q32]
Location_base_pair Starts at 185719874 and ends at 185739093 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)LOC101927196  101927196  uncharacterized LOC101927196
Aliases
GeneCards (Weizmann)LOC101927196
Ensembl hg19 (Hinxton)ENSG00000226747 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000226747 [Gene_View]  chr2:185719874-185739093 [Contig_View]  LOC101927196 [Vega]
ICGC DataPortalENSG00000226747
TCGA cBioPortalLOC101927196
AceView (NCBI)LOC101927196
Genatlas (Paris)LOC101927196
WikiGenes101927196
SOURCE (Princeton)LOC101927196
Genetics Home Reference (NIH)LOC101927196
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927196  -     chr2:185719874-185739093 -  2q32.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927196  -     2q32.1   [Description]    (hg19-Feb_2009)
EnsemblLOC101927196 - 2q32.1 [CytoView hg19]  LOC101927196 - 2q32.1 [CytoView hg38]
Mapping of homologs : NCBILOC101927196 [Mapview hg19]  LOC101927196 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC039382 BQ429883 BU561233 HY037094 HY052589
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927196
Cluster EST : UnigeneHs.244783 [ NCBI ]
CGAP (NCI)Hs.244783
Alternative Splicing GalleryENSG00000226747
Gene ExpressionLOC101927196 [ NCBI-GEO ]   LOC101927196 [ EBI - ARRAY_EXPRESS ]   LOC101927196 [ SEEK ]   LOC101927196 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927196 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927196
GTEX Portal (Tissue expression)LOC101927196
Human Protein AtlasENSG00000226747-LOC101927196 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927196
DMDM Disease mutations101927196
Blocks (Seattle)LOC101927196
Human Protein Atlas [tissue]ENSG00000226747-LOC101927196 [tissue]
Protein Interaction databases
FunCoupENSG00000226747
BioGRIDLOC101927196
STRING (EMBL)LOC101927196
ZODIACLOC101927196
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927196
BioCentury BCIQLOC101927196
ClinGenLOC101927196
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927196
Clinical trialLOC101927196
Miscellaneous
canSAR (ICR)LOC101927196 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927196
EVEXLOC101927196
GoPubMedLOC101927196
iHOPLOC101927196
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 : Tue Nov 21 13:49:49 CET 2017

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