Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101926934 (uncharacterized LOC101926934)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101926934
Atlas_Id 78061
Location 6p12.3  [Link to chromosome band 6p12]
Location_base_pair Starts at 46670444 and ends at 46687833 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)LOC101926934  101926934  uncharacterized LOC101926934
Aliases
GeneCards (Weizmann)LOC101926934
Ensembl hg19 (Hinxton)ENSG00000242973 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000242973 [Gene_View]  ENSG00000242973 [Sequence]  chr6:46670444-46687833 [Contig_View]  LOC101926934 [Vega]
ICGC DataPortalENSG00000242973
TCGA cBioPortalLOC101926934
AceView (NCBI)LOC101926934
Genatlas (Paris)LOC101926934
WikiGenes101926934
SOURCE (Princeton)LOC101926934
Genetics Home Reference (NIH)LOC101926934
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101926934  -     chr6:46670444-46687833 -  6p12.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101926934  -     6p12.3   [Description]    (hg19-Feb_2009)
EnsemblLOC101926934 - 6p12.3 [CytoView hg19]  LOC101926934 - 6p12.3 [CytoView hg38]
Mapping of homologs : NCBILOC101926934 [Mapview hg19]  LOC101926934 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AA725776 AI638322 AI698692 BX114358
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101926934
Cluster EST : UnigeneHs.664979 [ NCBI ]
CGAP (NCI)Hs.664979
Alternative Splicing GalleryENSG00000242973
Gene ExpressionLOC101926934 [ NCBI-GEO ]   LOC101926934 [ EBI - ARRAY_EXPRESS ]   LOC101926934 [ SEEK ]   LOC101926934 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101926934 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101926934
GTEX Portal (Tissue expression)LOC101926934
Human Protein AtlasENSG00000242973-LOC101926934 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101926934
DMDM Disease mutations101926934
Blocks (Seattle)LOC101926934
Human Protein Atlas [tissue]ENSG00000242973-LOC101926934 [tissue]
Protein Interaction databases
FunCoupENSG00000242973
BioGRIDLOC101926934
STRING (EMBL)LOC101926934
ZODIACLOC101926934
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101926934
BioCentury BCIQLOC101926934
ClinGenLOC101926934
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101926934
Clinical trialLOC101926934
Miscellaneous
canSAR (ICR)LOC101926934 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101926934
EVEXLOC101926934
GoPubMedLOC101926934
iHOPLOC101926934
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Jul 30 14:01:42 CEST 2018

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