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LOC105376166 (uncharacterized LOC105376166)


Other alias-
HGNC (Hugo) -
LocusID (NCBI) 105376166
Atlas_Id 76921
Location 9q22.33  [Link to chromosome band 9q22]
Location_base_pair Starts at 97120906 and ends at 97131010 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)

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

External links

<\ABLE$WiDTH=100%>Nomenclature HGNC (Hugo)-   - Cards Entrez_Gene (NCBI)LOC105376166  105376166  uncharacterized LOC105376166 Aliases GeneCards (Weizmann)LOC105376166 Ensembl hg19 (Hinxton) [Gene_View] Ensembl hg38 (Hinxton) [Gene_View]  chr9:97120906-97131010 [Contig_View]  LOC105376166 [Vega] TCGA cBioPortalLOC105376166 AceView (NCBI)LOC105376166 Genatlas (Paris)LOC105376166 WikiGenes105376166 SOURCE (Princeton)LOC105376166 Genetics Home Reference (NIH)LOC105376166 Genomic and cartography GoldenPath hg38 (UCSC)LOC105376166  -     chr9:97120906-97131010 -  9q22.33   [Description]    (hg38-Dec_2013) GoldenPath hg19 (UCSC)LOC105376166  -     9q22.33   [Description]    (hg19-Feb_2009) EnsemblLOC105376166 - 9q22.33 [CytoView hg19]  LOC105376166 - 9q22.33 [CytoView hg38] Mapping of homologs : NCBILOC105376166 [Mapview hg19]  LOC105376166 [Mapview hg38] Gene and transcription Genbank (Entrez)AK091930 RefSeq transcript (Entrez) RefSeq genomic (Entrez) Consensus coding sequences : CCDS (NCBI)LOC105376166 Cluster EST : UnigeneHs.434529 [ NCBI ] CGAP (NCI)Hs.434529 Gene ExpressionLOC105376166 [ NCBI-GEO ]   LOC105376166 [ EBI - ARRAY_EXPRESS ]   LOC105376166 [ SEEK ]   LOC105376166 [ MEM ] Gene Expression Viewer (FireBrowse)LOC105376166 [ Firebrowse - Broad ] SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60] BioGPS (Tissue expression)105376166 GTEX Portal (Tissue expression)LOC105376166 Protein : pattern, domain, 3D structure Domain families : Pfam (Sanger) Domain families : Pfam (NCBI) Conserved Domain (NCBI)LOC105376166 DMDM Disease mutations105376166 Blocks (Seattle)LOC105376166 Protein Interaction databases BioGRIDLOC105376166 STRING (EMBL)LOC105376166 ZODIACLOC105376166 Ontologies - Pathways Huge Navigator - [HugePedia] snp3D : Map Gene to Disease105376166 BioCentury BCIQLOC105376166 ClinGenLOC105376166 Clinical trials, drugs, therapyChemical/Protein Interactions : CTD105376166 Clinical trialLOC105376166 MiscellaneouscanSAR (ICR)LOC105376166 (select the gene name) ProbesLitteraturePubMed1 Pubmed reference(s) in Entrez GeneRIFsGene References Into Functions (Entrez) CoreMineLOC105376166 EVEXLOC105376166 GoPubMedLOC105376166 iHOPLOC105376166

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indexed on : Tue Nov 21 13:54:49 CET 2017

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