Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101929523 (uncharacterized LOC101929523)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929523
Atlas_Id 78097
Location 6q27  [Link to chromosome band 6q27]
Location_base_pair Starts at 169213212 and ends at 169239562 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)LOC101929523  101929523  uncharacterized LOC101929523
Aliases
GeneCards (Weizmann)LOC101929523
Ensembl hg19 (Hinxton)ENSG00000226445 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000226445 [Gene_View]  ENSG00000226445 [Sequence]  chr6:169213212-169239562 [Contig_View]  LOC101929523 [Vega]
ICGC DataPortalENSG00000226445
TCGA cBioPortalLOC101929523
AceView (NCBI)LOC101929523
Genatlas (Paris)LOC101929523
WikiGenes101929523
SOURCE (Princeton)LOC101929523
Genetics Home Reference (NIH)LOC101929523
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929523  -     chr6:169213212-169239562 +  6q27   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929523  -     6q27   [Description]    (hg19-Feb_2009)
EnsemblLOC101929523 - 6q27 [CytoView hg19]  LOC101929523 - 6q27 [CytoView hg38]
Mapping of homologs : NCBILOC101929523 [Mapview hg19]  LOC101929523 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BI755364
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929523
Cluster EST : UnigeneHs.442696 [ NCBI ]
CGAP (NCI)Hs.442696
Alternative Splicing GalleryENSG00000226445
Gene ExpressionLOC101929523 [ NCBI-GEO ]   LOC101929523 [ EBI - ARRAY_EXPRESS ]   LOC101929523 [ SEEK ]   LOC101929523 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929523 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929523
GTEX Portal (Tissue expression)LOC101929523
Human Protein AtlasENSG00000226445-LOC101929523 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929523
DMDM Disease mutations101929523
Blocks (Seattle)LOC101929523
Human Protein Atlas [tissue]ENSG00000226445-LOC101929523 [tissue]
Protein Interaction databases
FunCoupENSG00000226445
BioGRIDLOC101929523
STRING (EMBL)LOC101929523
ZODIACLOC101929523
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929523
BioCentury BCIQLOC101929523
ClinGenLOC101929523
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929523
Clinical trialLOC101929523
Miscellaneous
canSAR (ICR)LOC101929523 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929523
EVEXLOC101929523
GoPubMedLOC101929523
iHOPLOC101929523
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 14:04:31 CEST 2018

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