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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)

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

8TD WKDDH=15%>STRING (EMBL)
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
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 AtlasENSG00000230920
Protein Interaction databases
FunCoupENSG00000230920
BioGRIDLOC105375972
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 (Entre{)<+A>
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 : Mon Sep 18 13:23:45 CEST 2017

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