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LOC105369213 (uncharacterized LOC105369213)

Identity

Alias (NCBI)-
HGNC (Hugo) -
LocusID (NCBI) 105369213
Atlas_Id 78624
Location 16q23.3  [Link to chromosome band 16q23]
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


External links

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)LOC105369213  105369213  uncharacterized LOC105369213
Aliases
GeneCards (Weizmann)LOC105369213
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]   [Sequence]  - [Contig_View]  LOC105369213 [Vega]
TCGA cBioPortalLOC105369213
AceView (NCBI)LOC105369213
Genatlas (Paris)LOC105369213
WikiGenes105369213
SOURCE (Princeton)LOC105369213
Genetics Home Reference (NIH)LOC105369213
Genomic and cartography
GoldenPath hg38 (UCSC)LOC105369213  -  
GoldenPath hg19 (UCSC)LOC105369213  -  
GoldenPathLOC105369213 - [CytoView hg19]  LOC105369213 - [CytoView hg38]
genome Data Viewer NCBILOC105369213 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)BC040927
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC105369213
Gene ExpressionLOC105369213 [ NCBI-GEO ]   LOC105369213 [ EBI - ARRAY_EXPRESS ]   LOC105369213 [ SEEK ]   LOC105369213 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC105369213 [ Firebrowse - Broad ]
GenevisibleExpression of LOC105369213 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)105369213
GTEX Portal (Tissue expression)LOC105369213
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC105369213
DMDM Disease mutations105369213
Blocks (Seattle)LOC105369213
Protein Interaction databases
BioGRIDLOC105369213
STRING (EMBL)LOC105369213
ZODIACLOC105369213
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease105369213
BioCentury BCIQLOC105369213
ClinGenLOC105369213
Clinical trials, drugs, therapy
Protein Interactions : CTD105369213
Clinical trialLOC105369213
Miscellaneous
canSAR (ICR)LOC105369213 (select the gene name)
HarmonizomeLOC105369213
DataMed IndexLOC105369213
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC105369213
EVEXLOC105369213
GoPubMedLOC105369213
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 : Thu Jul 16 16:09:55 CEST 2020

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