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LOC101926898 (uncharacterized LOC101926898)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101926898
Atlas_Id 67008
Location 6p12.3  [Link to chromosome band 6p12]
Location_base_pair Starts at 46492052 and ends at 46533480 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)LOC101926898  101926898  uncharacterized LOC101926898
Aliases
GeneCards (Weizmann)LOC101926898
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]   [Sequence]  chr6:46492052-46533480 [Contig_View]  LOC101926898 [Vega]
TCGA cBioPortalLOC101926898
AceView (NCBI)LOC101926898
Genatlas (Paris)LOC101926898
WikiGenes101926898
SOURCE (Princeton)LOC101926898
Genetics Home Reference (NIH)LOC101926898
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101926898  -     chr6:46492052-46533480 +  6p12.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101926898  -     6p12.3   [Description]    (hg19-Feb_2009)
EnsemblLOC101926898 - 6p12.3 [CytoView hg19]  LOC101926898 - 6p12.3 [CytoView hg38]
Mapping of homologs : NCBILOC101926898 [Mapview hg19]  LOC101926898 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC042616
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101926898
Cluster EST : UnigeneHs.639416 [ NCBI ]
CGAP (NCI)Hs.639416
Gene ExpressionLOC101926898 [ NCBI-GEO ]   LOC101926898 [ EBI - ARRAY_EXPRESS ]   LOC101926898 [ SEEK ]   LOC101926898 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101926898 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101926898
GTEX Portal (Tissue expression)LOC101926898
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101926898
DMDM Disease mutations101926898
Blocks (Seattle)LOC101926898
Protein Interaction databases
BioGRIDLOC101926898
STRING (EMBL)LOC101926898
ZODIACLOC101926898
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101926898
BioCentury BCIQLOC101926898
ClinGenLOC101926898
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101926898
Clinical trialLOC101926898
Miscellaneous
canSAR (ICR)LOC101926898 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101926898
EVEXLOC101926898
GoPubMedLOC101926898
iHOPLOC101926898
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 : Mon Jul 30 14:01:40 CEST 2018

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