Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101926942 (uncharacterized LOC101926942)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101926942
Atlas_Id 67020
Location 10q23.31  [Link to chromosome band 10q23]
Location_base_pair Starts at 90402521 and ends at 90540805 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)LOC101926942  101926942  uncharacterized LOC101926942
Aliases
GeneCards (Weizmann)LOC101926942
Ensembl hg19 (Hinxton)ENSG00000236373 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000236373 [Gene_View]  chr10:90402521-90540805 [Contig_View]  LOC101926942 [Vega]
ICGC DataPortalENSG00000236373
TCGA cBioPortalLOC101926942
AceView (NCBI)LOC101926942
Genatlas (Paris)LOC101926942
WikiGenes101926942
SOURCE (Princeton)LOC101926942
Genetics Home Reference (NIH)LOC101926942
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101926942  -     chr10:90402521-90540805 -  10q23.31   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101926942  -     10q23.31   [Description]    (hg19-Feb_2009)
EnsemblLOC101926942 - 10q23.31 [CytoView hg19]  LOC101926942 - 10q23.31 [CytoView hg38]
Mapping of homologs : NCBILOC101926942 [Mapview hg19]  LOC101926942 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC030278
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101926942
Cluster EST : UnigeneHs.382666 [ NCBI ]
CGAP (NCI)Hs.382666
Alternative Splicing GalleryENSG00000236373
Gene ExpressionLOC101926942 [ NCBI-GEO ]   LOC101926942 [ EBI - ARRAY_EXPRESS ]   LOC101926942 [ SEEK ]   LOC101926942 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101926942 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101926942
GTEX Portal (Tissue expression)LOC101926942
Human Protein AtlasENSG00000236373-LOC101926942 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101926942
DMDM Disease mutations101926942
Blocks (Seattle)LOC101926942
Human Protein Atlas [tissue]ENSG00000236373-LOC101926942 [tissue]
Protein Interaction databases
FunCoupENSG00000236373
BioGRIDLOC101926942
STRING (EMBL)LOC101926942
ZODIACLOC101926942
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101926942
BioCentury BCIQLOC101926942
ClinGenLOC101926942
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101926942
Clinical trialLOC101926942
Miscellaneous
canSAR (ICR)LOC101926942 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101926942
EVEXLOC101926942
GoPubMedLOC101926942
iHOPLOC101926942
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 13:49:33 CET 2017

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