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LOC101926969 (uncharacterized LOC101926969)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101926969
Atlas_Id 77496
Location 2p11.2  [Link to chromosome band 2p11]
Location_base_pair Starts at 91580336 and ends at 91580863 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


External links

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)LOC101926969  101926969  uncharacterized LOC101926969
Aliases
GeneCards (Weizmann)LOC101926969
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr2:91580336-91580863 [Contig_View]  LOC101926969 [Vega]
TCGA cBioPortalLOC101926969
AceView (NCBI)LOC101926969
Genatlas (Paris)LOC101926969
WikiGenes101926969
SOURCE (Princeton)LOC101926969
Genetics Home Reference (NIH)LOC101926969
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101926969  -     chr2:91580336-91580863 +  2p11.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101926969  -     2p11.2   [Description]    (hg19-Feb_2009)
EnsemblLOC101926969 - 2p11.2 [CytoView hg19]  LOC101926969 - 2p11.2 [CytoView hg38]
Mapping of homologs : NCBILOC101926969 [Mapview hg19]  LOC101926969 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AF086033
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101926969
Cluster EST : UnigeneHs.696606 [ NCBI ]
CGAP (NCI)Hs.696606
Gene ExpressionLOC101926969 [ NCBI-GEO ]   LOC101926969 [ EBI - ARRAY_EXPRESS ]   LOC101926969 [ SEEK ]   LOC101926969 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101926969 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101926969
GTEX Portal (Tissue expression)LOC101926969
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101926969
DMDM Disease mutations101926969
Blocks (Seattle)LOC101926969
Protein Interaction databases
BioGRIDLOC101926969
STRING (EMBL)LOC101926969
ZODIACLOC101926969
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101926969
BioCentury BCIQLOC101926969
ClinGenLOC101926969
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101926969
Clinical trialLOC101926969
Miscellaneous
canSAR (ICR)LOC101926969 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101926969
EVEXLOC101926969
GoPubMedLOC101926969
iHOPLOC101926969
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 : Tue Nov 21 13:49:36 CET 2017

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