Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101929460 (uncharacterized LOC101929460)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929460
Atlas_Id 77089
Location 6q27  [Link to chromosome band 6q27]
Location_base_pair Starts at 169034171 and ends at 169035643 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)LOC101929460  101929460  uncharacterized LOC101929460
Aliases
GeneCards (Weizmann)LOC101929460
Ensembl hg19 (Hinxton)ENSG00000229720 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000229720 [Gene_View]  ENSG00000229720 [Sequence]  chr6:169034171-169035643 [Contig_View]  LOC101929460 [Vega]
ICGC DataPortalENSG00000229720
TCGA cBioPortalLOC101929460
AceView (NCBI)LOC101929460
Genatlas (Paris)LOC101929460
WikiGenes101929460
SOURCE (Princeton)LOC101929460
Genetics Home Reference (NIH)LOC101929460
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929460  -     chr6:169034171-169035643 -  6q27   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929460  -     6q27   [Description]    (hg19-Feb_2009)
EnsemblLOC101929460 - 6q27 [CytoView hg19]  LOC101929460 - 6q27 [CytoView hg38]
Mapping of homologs : NCBILOC101929460 [Mapview hg19]  LOC101929460 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC040917
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929460
Cluster EST : UnigeneHs.355225 [ NCBI ]
CGAP (NCI)Hs.355225
Alternative Splicing GalleryENSG00000229720
Gene ExpressionLOC101929460 [ NCBI-GEO ]   LOC101929460 [ EBI - ARRAY_EXPRESS ]   LOC101929460 [ SEEK ]   LOC101929460 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929460 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929460
GTEX Portal (Tissue expression)LOC101929460
Human Protein AtlasENSG00000229720-LOC101929460 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929460
DMDM Disease mutations101929460
Blocks (Seattle)LOC101929460
Human Protein Atlas [tissue]ENSG00000229720-LOC101929460 [tissue]
Protein Interaction databases
FunCoupENSG00000229720
BioGRIDLOC101929460
STRING (EMBL)LOC101929460
ZODIACLOC101929460
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929460
BioCentury BCIQLOC101929460
ClinGenLOC101929460
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929460
Clinical trialLOC101929460
Miscellaneous
canSAR (ICR)LOC101929460 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929460
EVEXLOC101929460
GoPubMedLOC101929460
iHOPLOC101929460
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 : Mon Jul 30 14:04:28 CEST 2018

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