Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101929439 (uncharacterized LOC101929439)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929439
Atlas_Id 67555
Location 15q24.2  [Link to chromosome band 15q24]
Location_base_pair Starts at 76174891 and ends at 76181486 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)LOC101929439  101929439  uncharacterized LOC101929439
Aliases
GeneCards (Weizmann)LOC101929439
Ensembl hg19 (Hinxton)ENSG00000259422 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000259422 [Gene_View]  chr15:76174891-76181486 [Contig_View]  LOC101929439 [Vega]
ICGC DataPortalENSG00000259422
TCGA cBioPortalLOC101929439
AceView (NCBI)LOC101929439
Genatlas (Paris)LOC101929439
WikiGenes101929439
SOURCE (Princeton)LOC101929439
Genetics Home Reference (NIH)LOC101929439
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929439  -     chr15:76174891-76181486 -  15q24.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929439  -     15q24.2   [Description]    (hg19-Feb_2009)
EnsemblLOC101929439 - 15q24.2 [CytoView hg19]  LOC101929439 - 15q24.2 [CytoView hg38]
Mapping of homologs : NCBILOC101929439 [Mapview hg19]  LOC101929439 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK127738
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929439
Cluster EST : UnigeneHs.631721 [ NCBI ]
CGAP (NCI)Hs.631721
Alternative Splicing GalleryENSG00000259422
Gene ExpressionLOC101929439 [ NCBI-GEO ]   LOC101929439 [ EBI - ARRAY_EXPRESS ]   LOC101929439 [ SEEK ]   LOC101929439 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929439 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929439
GTEX Portal (Tissue expression)LOC101929439
Human Protein AtlasENSG00000259422-LOC101929439 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929439
DMDM Disease mutations101929439
Blocks (Seattle)LOC101929439
Human Protein Atlas [tissue]ENSG00000259422-LOC101929439 [tissue]
Protein Interaction databases
FunCoupENSG00000259422
BioGRIDLOC101929439
STRING (EMBL)LOC101929439
ZODIACLOC101929439
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929439
BioCentury BCIQLOC101929439
ClinGenLOC101929439
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929439
Clinical trialLOC101929439
Miscellaneous
canSAR (ICR)LOC101929439 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929439
EVEXLOC101929439
GoPubMedLOC101929439
iHOPLOC101929439
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 12:05:18 CET 2017

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