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LOC105371795 (uncharacterized LOC105371795)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 105371795
Atlas_Id 78346
Location 17q21.31  [Link to chromosome band 17q21]
Location_base_pair Starts at 45168805 and ends at 45171485 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

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)LOC105371795  105371795  uncharacterized LOC105371795
Aliases
GeneCards (Weizmann)LOC105371795
Ensembl hg19 (Hinxton)ENSG00000267288 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000267288 [Gene_View]  chr17:45168805-45171485 [Contig_View]  LOC105371795 [Vega]
ICGC DataPortalENSG00000267288
TCGA cBioPortalLOC105371795
AceView (NCBI)LOC105371795
Genatlas (Paris)LOC105371795
WikiGenes105371795
SOURCE (Princeton)LOC105371795
Genetics Home Reference (NIH)LOC105371795
Genomic and cartography
GoldenPath hg38 (UCSC)LOC105371795  -     chr17:45168805-45171485 -  17q21.31   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC105371795  -     17q21.31   [Description]    (hg19-Feb_2009)
EnsemblLOC105371795 - 17q21.31 [CytoView hg19]  LOC105371795 - 17q21.31 [CytoView hg38]
Mapping of homologs : NCBILOC105371795 [Mapview hg19]  LOC105371795 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK096785 DA634757
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC105371795
Cluster EST : UnigeneHs.569733 [ NCBI ]
CGAP (NCI)Hs.569733
Alternative Splicing GalleryENSG00000267288
Gene ExpressionLOC105371795 [ NCBI-GEO ]   LOC105371795 [ EBI - ARRAY_EXPRESS ]   LOC105371795 [ SEEK ]   LOC105371795 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC105371795 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)105371795
GTEX Portal (Tissue expression)LOC105371795
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC105371795
DMDM Disease mutations105371795
Blocks (Seattle)LOC105371795
Human Protein AtlasENSG00000267288
Protein Interaction databases
FunCoupENSG00000267288
BioGRIDLOC105371795
STRING (EMBL)LOC105371795
ZODIACLOC105371795
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease105371795
BioCentury BCIQLOC105371795
ClinGenLOC105371795
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD105371795
Clinical trialLOC105371795
Miscellaneous
canSAR (ICR)LOC105371795 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC105371795
EVEXLOC105371795
GoPubMedLOC105371795
iHOPLOC105371795
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Sep 18 13:23:09 CEST 2017

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