Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101928489 (uncharacterized LOC101928489)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928489
Atlas_Id 67367
Location 6q13  [Link to chromosome band 6q13]
Location_base_pair Starts at 73693903 and ends at 73696131 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)LOC101928489  101928489  uncharacterized LOC101928489
Aliases
GeneCards (Weizmann)LOC101928489
Ensembl hg19 (Hinxton)ENSG00000231652 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000231652 [Gene_View]  ENSG00000231652 [Sequence]  chr6:73693903-73696131 [Contig_View]  LOC101928489 [Vega]
ICGC DataPortalENSG00000231652
TCGA cBioPortalLOC101928489
AceView (NCBI)LOC101928489
Genatlas (Paris)LOC101928489
WikiGenes101928489
SOURCE (Princeton)LOC101928489
Genetics Home Reference (NIH)LOC101928489
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101928489  -     chr6:73693903-73696131 -  6q13   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101928489  -     6q13   [Description]    (hg19-Feb_2009)
EnsemblLOC101928489 - 6q13 [CytoView hg19]  LOC101928489 - 6q13 [CytoView hg38]
Mapping of homologs : NCBILOC101928489 [Mapview hg19]  LOC101928489 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK124950 BQ021047
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101928489
Cluster EST : UnigeneHs.660059 [ NCBI ]
CGAP (NCI)Hs.660059
Alternative Splicing GalleryENSG00000231652
Gene ExpressionLOC101928489 [ NCBI-GEO ]   LOC101928489 [ EBI - ARRAY_EXPRESS ]   LOC101928489 [ SEEK ]   LOC101928489 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928489 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928489
GTEX Portal (Tissue expression)LOC101928489
Human Protein AtlasENSG00000231652-LOC101928489 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928489
DMDM Disease mutations101928489
Blocks (Seattle)LOC101928489
Human Protein Atlas [tissue]ENSG00000231652-LOC101928489 [tissue]
Protein Interaction databases
FunCoupENSG00000231652
BioGRIDLOC101928489
STRING (EMBL)LOC101928489
ZODIACLOC101928489
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928489
BioCentury BCIQLOC101928489
ClinGenLOC101928489
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928489
Clinical trialLOC101928489
Miscellaneous
canSAR (ICR)LOC101928489 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101928489
EVEXLOC101928489
GoPubMedLOC101928489
iHOPLOC101928489
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Jul 30 14:03:30 CEST 2018

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