Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC105375972 (uncharacterized LOC105375972)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 105375972
Atlas_Id 78275
Location 9p23  [Link to chromosome band 9p23]
Location_base_pair Starts at 9799392 and ends at 9803787 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)LOC105375972  105375972  uncharacterized LOC105375972
Aliases
GeneCards (Weizmann)LOC105375972
Ensembl hg19 (Hinxton)ENSG00000230920 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000230920 [Gene_View]  chr9:9799392-9803787 [Contig_View]  LOC105375972 [Vega]
ICGC DataPortalENSG00000230920
TCGA cBioPortalLOC105375972
AceView (NCBI)LOC105375972
Genatlas (Paris)LOC105375972
WikiGenes105375972
SOURCE (Princeton)LOC105375972
Genetics Home Reference (NIH)LOC105375972
Genomic and cartography
GoldenPath hg38 (UCSC)LOC105375972  -     chr9:9799392-9803787 +  9p23   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC105375972  -     9p23   [Description]    (hg19-Feb_2009)
EnsemblLOC105375972 - 9p23 [CytoView hg19]  LOC105375972 - 9p23 [CytoView hg38]
Mapping of homologs : NCBILOC105375972 [Mapview hg19]  LOC105375972 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BX105718
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC105375972
Cluster EST : UnigeneHs.738242 [ NCBI ]
CGAP (NCI)Hs.738242
Alternative Splicing GalleryENSG00000230920
Gene ExpressionLOC105375972 [ NCBI-GEO ]   LOC105375972 [ EBI - ARRAY_EXPRESS ]   LOC105375972 [ SEEK ]   LOC105375972 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC105375972 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)105375972
GTEX Portal (Tissue expression)LOC105375972
Human Protein AtlasENSG00000230920-LOC105375972 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC105375972
DMDM Disease mutations105375972
Blocks (Seattle)LOC105375972
Human Protein Atlas [tissue]ENSG00000230920-LOC105375972 [tissue]
Protein Interaction databases
FunCoupENSG00000230920
BioGRIDLOC105375972
STRING (EMBL)LOC105375972
ZODIACLOC105375972
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease105375972
BioCentury BCIQLOC105375972
ClinGenLOC105375972
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD105375972
Clinical trialLOC105375972
Miscellaneous
canSAR (ICR)LOC105375972 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC105375972
EVEXLOC105375972
GoPubMedLOC105375972
iHOPLOC105375972
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Tue Nov 21 13:54:46 CET 2017

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