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LOC105377962 (uncharacterized LOC105377962)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 105377962
Atlas_Id 78044
Location 6q22.1  [Link to chromosome band 6q22]
Location_base_pair Starts at 115633542 and ends at 115643835 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)LOC105377962  105377962  uncharacterized LOC105377962
Aliases
GeneCards (Weizmann)LOC105377962
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]   [Sequence]  chr6:115633542-115643835 [Contig_View]  LOC105377962 [Vega]
TCGA cBioPortalLOC105377962
AceView (NCBI)LOC105377962
Genatlas (Paris)LOC105377962
WikiGenes105377962
SOURCE (Princeton)LOC105377962
Genetics Home Reference (NIH)LOC105377962
Genomic and cartography
GoldenPath hg38 (UCSC)LOC105377962  -     chr6:115633542-115643835 -  6q22.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC105377962  -     6q22.1   [Description]    (hg19-Feb_2009)
EnsemblLOC105377962 - 6q22.1 [CytoView hg19]  LOC105377962 - 6q22.1 [CytoView hg38]
Mapping of homologs : NCBILOC105377962 [Mapview hg19]  LOC105377962 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AI215976 CR741031
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC105377962
Cluster EST : UnigeneHs.571066 [ NCBI ]
CGAP (NCI)Hs.571066
Gene ExpressionLOC105377962 [ NCBI-GEO ]   LOC105377962 [ EBI - ARRAY_EXPRESS ]   LOC105377962 [ SEEK ]   LOC105377962 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC105377962 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)105377962
GTEX Portal (Tissue expression)LOC105377962
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC105377962
DMDM Disease mutations105377962
Blocks (Seattle)LOC105377962
Protein Interaction databases
BioGRIDLOC105377962
STRING (EMBL)LOC105377962
ZODIACLOC105377962
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease105377962
BioCentury BCIQLOC105377962
ClinGenLOC105377962
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD105377962
Clinical trialLOC105377962
Miscellaneous
canSAR (ICR)LOC105377962 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC105377962
EVEXLOC105377962
GoPubMedLOC105377962
iHOPLOC105377962
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 Jul 30 14:07:49 CEST 2018

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