Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101928797 (uncharacterized LOC101928797)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928797
Atlas_Id 67435
Location 9q33.1  [Link to chromosome band 9q33]
Location_base_pair Starts at 117648606 and ends at 117657026 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)LOC101928797  101928797  uncharacterized LOC101928797
Aliases
GeneCards (Weizmann)LOC101928797
Ensembl hg19 (Hinxton)ENSG00000233569 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000233569 [Gene_View]  chr9:117648606-117657026 [Contig_View]  LOC101928797 [Vega]
ICGC DataPortalENSG00000233569
TCGA cBioPortalLOC101928797
AceView (NCBI)LOC101928797
Genatlas (Paris)LOC101928797
WikiGenes101928797
SOURCE (Princeton)LOC101928797
Genetics Home Reference (NIH)LOC101928797
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101928797  -     chr9:117648606-117657026 +  9q33.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101928797  -     9q33.1   [Description]    (hg19-Feb_2009)
EnsemblLOC101928797 - 9q33.1 [CytoView hg19]  LOC101928797 - 9q33.1 [CytoView hg38]
Mapping of homologs : NCBILOC101928797 [Mapview hg19]  LOC101928797 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC034724
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101928797
Cluster EST : UnigeneHs.382317 [ NCBI ]
CGAP (NCI)Hs.382317
Alternative Splicing GalleryENSG00000233569
Gene ExpressionLOC101928797 [ NCBI-GEO ]   LOC101928797 [ EBI - ARRAY_EXPRESS ]   LOC101928797 [ SEEK ]   LOC101928797 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928797 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928797
GTEX Portal (Tissue expression)LOC101928797
Human Protein AtlasENSG00000233569-LOC101928797 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928797
DMDM Disease mutations101928797
Blocks (Seattle)LOC101928797
Human Protein Atlas [tissue]ENSG00000233569-LOC101928797 [tissue]
Protein Interaction databases
FunCoupENSG00000233569
BioGRIDLOC101928797
STRING (EMBL)LOC101928797
ZODIACLOC101928797
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928797
BioCentury BCIQLOC101928797
ClinGenLOC101928797
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928797
Clinical trialLOC101928797
Miscellaneous
canSAR (ICR)LOC101928797 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101928797
EVEXLOC101928797
GoPubMedLOC101928797
iHOPLOC101928797
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 : Tue Nov 21 13:51:33 CET 2017

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