Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101929497 (uncharacterized LOC101929497)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929497
Atlas_Id 67568
Location 11q24.2  [Link to chromosome band 11q24]
Location_base_pair Starts at 127271070 and ends at 127337033 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)LOC101929497  101929497  uncharacterized LOC101929497
Aliases
GeneCards (Weizmann)LOC101929497
Ensembl hg19 (Hinxton)ENSG00000273409 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000273409 [Gene_View]  chr11:127271070-127337033 [Contig_View]  LOC101929497 [Vega]
ICGC DataPortalENSG00000273409
TCGA cBioPortalLOC101929497
AceView (NCBI)LOC101929497
Genatlas (Paris)LOC101929497
WikiGenes101929497
SOURCE (Princeton)LOC101929497
Genetics Home Reference (NIH)LOC101929497
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929497  -     chr11:127271070-127337033 +  11q24.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929497  -     11q24.2   [Description]    (hg19-Feb_2009)
EnsemblLOC101929497 - 11q24.2 [CytoView hg19]  LOC101929497 - 11q24.2 [CytoView hg38]
Mapping of homologs : NCBILOC101929497 [Mapview hg19]  LOC101929497 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC030092 DB487307
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929497
Cluster EST : UnigeneHs.737442 [ NCBI ]
CGAP (NCI)Hs.737442
Alternative Splicing GalleryENSG00000273409
Gene ExpressionLOC101929497 [ NCBI-GEO ]   LOC101929497 [ EBI - ARRAY_EXPRESS ]   LOC101929497 [ SEEK ]   LOC101929497 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929497 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929497
GTEX Portal (Tissue expression)LOC101929497
Human Protein AtlasENSG00000273409-LOC101929497 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929497
DMDM Disease mutations101929497
Blocks (Seattle)LOC101929497
Human Protein Atlas [tissue]ENSG00000273409-LOC101929497 [tissue]
Protein Interaction databases
FunCoupENSG00000273409
BioGRIDLOC101929497
STRING (EMBL)LOC101929497
ZODIACLOC101929497
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929497
BioCentury BCIQLOC101929497
ClinGenLOC101929497
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929497
Clinical trialLOC101929497
Miscellaneous
canSAR (ICR)LOC101929497 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929497
EVEXLOC101929497
GoPubMedLOC101929497
iHOPLOC101929497
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Thu Nov 9 12:05:21 CET 2017

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