Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101929586 (uncharacterized LOC101929586)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929586
Atlas_Id 67592
Location 15q25.1  [Link to chromosome band 15q25]
Location_base_pair Starts at 80554611 and ends at 80562944 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)LOC101929586  101929586  uncharacterized LOC101929586
Aliases
GeneCards (Weizmann)LOC101929586
Ensembl hg19 (Hinxton)ENSG00000259175 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000259175 [Gene_View]  chr15:80554611-80562944 [Contig_View]  LOC101929586 [Vega]
ICGC DataPortalENSG00000259175
TCGA cBioPortalLOC101929586
AceView (NCBI)LOC101929586
Genatlas (Paris)LOC101929586
WikiGenes101929586
SOURCE (Princeton)LOC101929586
Genetics Home Reference (NIH)LOC101929586
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929586  -     chr15:80554611-80562944 -  15q25.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929586  -     15q25.1   [Description]    (hg19-Feb_2009)
EnsemblLOC101929586 - 15q25.1 [CytoView hg19]  LOC101929586 - 15q25.1 [CytoView hg38]
Mapping of homologs : NCBILOC101929586 [Mapview hg19]  LOC101929586 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC041477
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929586
Cluster EST : UnigeneHs.569426 [ NCBI ]
CGAP (NCI)Hs.569426
Alternative Splicing GalleryENSG00000259175
Gene ExpressionLOC101929586 [ NCBI-GEO ]   LOC101929586 [ EBI - ARRAY_EXPRESS ]   LOC101929586 [ SEEK ]   LOC101929586 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929586 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929586
GTEX Portal (Tissue expression)LOC101929586
Human Protein AtlasENSG00000259175-LOC101929586 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929586
DMDM Disease mutations101929586
Blocks (Seattle)LOC101929586
Human Protein Atlas [tissue]ENSG00000259175-LOC101929586 [tissue]
Protein Interaction databases
FunCoupENSG00000259175
BioGRIDLOC101929586
STRING (EMBL)LOC101929586
ZODIACLOC101929586
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929586
BioCentury BCIQLOC101929586
ClinGenLOC101929586
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929586
Clinical trialLOC101929586
Miscellaneous
canSAR (ICR)LOC101929586 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929586
EVEXLOC101929586
GoPubMedLOC101929586
iHOPLOC101929586
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 : Thu Nov 9 12:05:28 CET 2017

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