Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101926962 (uncharacterized LOC101926962)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101926962
Atlas_Id 67025
Location 6p12.3  [Link to chromosome band 6p12]
Location_base_pair Starts at 46903471 and ends at 46910027 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)LOC101926962  101926962  uncharacterized LOC101926962
Aliases
GeneCards (Weizmann)LOC101926962
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]   [Sequence]  chr6:46903471-46910027 [Contig_View]  LOC101926962 [Vega]
TCGA cBioPortalLOC101926962
AceView (NCBI)LOC101926962
Genatlas (Paris)LOC101926962
WikiGenes101926962
SOURCE (Princeton)LOC101926962
Genetics Home Reference (NIH)LOC101926962
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101926962  -     chr6:46903471-46910027 +  6p12.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101926962  -     6p12.3   [Description]    (hg19-Feb_2009)
EnsemblLOC101926962 - 6p12.3 [CytoView hg19]  LOC101926962 - 6p12.3 [CytoView hg38]
Mapping of homologs : NCBILOC101926962 [Mapview hg19]  LOC101926962 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC042990
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101926962
Cluster EST : UnigeneHs.680113 [ NCBI ]
CGAP (NCI)Hs.680113
Gene ExpressionLOC101926962 [ NCBI-GEO ]   LOC101926962 [ EBI - ARRAY_EXPRESS ]   LOC101926962 [ SEEK ]   LOC101926962 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101926962 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101926962
GTEX Portal (Tissue expression)LOC101926962
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101926962
DMDM Disease mutations101926962
Blocks (Seattle)LOC101926962
Protein Interaction databases
BioGRIDLOC101926962
STRING (EMBL)LOC101926962
ZODIACLOC101926962
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101926962
BioCentury BCIQLOC101926962
ClinGenLOC101926962
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101926962
Clinical trialLOC101926962
Miscellaneous
canSAR (ICR)LOC101926962 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101926962
EVEXLOC101926962
GoPubMedLOC101926962
iHOPLOC101926962
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 14:01:44 CEST 2018

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