Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101929504 (uncharacterized LOC101929504)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929504
Atlas_Id 67569
Location 6q27  [Link to chromosome band 6q27]
Location_base_pair Starts at 169175304 and ends at 169182740 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)LOC101929504  101929504  uncharacterized LOC101929504
Aliases
GeneCards (Weizmann)LOC101929504
Ensembl hg19 (Hinxton)ENSG00000261039 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000261039 [Gene_View]  ENSG00000261039 [Sequence]  chr6:169175304-169182740 [Contig_View]  LOC101929504 [Vega]
ICGC DataPortalENSG00000261039
TCGA cBioPortalLOC101929504
AceView (NCBI)LOC101929504
Genatlas (Paris)LOC101929504
WikiGenes101929504
SOURCE (Princeton)LOC101929504
Genetics Home Reference (NIH)LOC101929504
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929504  -     chr6:169175304-169182740 -  6q27   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929504  -     6q27   [Description]    (hg19-Feb_2009)
EnsemblLOC101929504 - 6q27 [CytoView hg19]  LOC101929504 - 6q27 [CytoView hg38]
Mapping of homologs : NCBILOC101929504 [Mapview hg19]  LOC101929504 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AF086258
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929504
Cluster EST : UnigeneHs.147721 [ NCBI ]
CGAP (NCI)Hs.147721
Alternative Splicing GalleryENSG00000261039
Gene ExpressionLOC101929504 [ NCBI-GEO ]   LOC101929504 [ EBI - ARRAY_EXPRESS ]   LOC101929504 [ SEEK ]   LOC101929504 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929504 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929504
GTEX Portal (Tissue expression)LOC101929504
Human Protein AtlasENSG00000261039-LOC101929504 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929504
DMDM Disease mutations101929504
Blocks (Seattle)LOC101929504
Human Protein Atlas [tissue]ENSG00000261039-LOC101929504 [tissue]
Protein Interaction databases
FunCoupENSG00000261039
BioGRIDLOC101929504
STRING (EMBL)LOC101929504
ZODIACLOC101929504
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929504
BioCentury BCIQLOC101929504
ClinGenLOC101929504
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929504
Clinical trialLOC101929504
Miscellaneous
canSAR (ICR)LOC101929504 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929504
EVEXLOC101929504
GoPubMedLOC101929504
iHOPLOC101929504
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 14:04:30 CEST 2018

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