Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC105371789 (uncharacterized LOC105371789)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 105371789
Atlas_Id 78445
Location 17q21.31  [Link to chromosome band 17q21]
Location_base_pair Starts at 44115912 and ends at 44120595 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)LOC105371789  105371789  uncharacterized LOC105371789
Aliases
GeneCards (Weizmann)LOC105371789
Ensembl hg19 (Hinxton)ENSG00000267638 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000267638 [Gene_View]  chr17:44115912-44120595 [Contig_View]  LOC105371789 [Vega]
ICGC DataPortalENSG00000267638
TCGA cBioPortalLOC105371789
AceView (NCBI)LOC105371789
Genatlas (Paris)LOC105371789
WikiGenes105371789
SOURCE (Princeton)LOC105371789
Genetics Home Reference (NIH)LOC105371789
Genomic and cartography
GoldenPath hg38 (UCSC)LOC105371789  -     chr17:44115912-44120595 +  17q21.31   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC105371789  -     17q21.31   [Description]    (hg19-Feb_2009)
EnsemblLOC105371789 - 17q21.31 [CytoView hg19]  LOC105371789 - 17q21.31 [CytoView hg38]
Mapping of homologs : NCBILOC105371789 [Mapview hg19]  LOC105371789 [Mapview hg38]
Gene and transcription
Genbank (Entrez)DB338921
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC105371789
Cluster EST : UnigeneHs.579304 [ NCBI ]
CGAP (NCI)Hs.579304
Alternative Splicing GalleryENSG00000267638
Gene ExpressionLOC105371789 [ NCBI-GEO ]   LOC105371789 [ EBI - ARRAY_EXPRESS ]   LOC105371789 [ SEEK ]   LOC105371789 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC105371789 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)105371789
GTEX Portal (Tissue expression)LOC105371789
Human Protein AtlasENSG00000267638-LOC105371789 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC105371789
DMDM Disease mutations105371789
Blocks (Seattle)LOC105371789
Human Protein Atlas [tissue]ENSG00000267638-LOC105371789 [tissue]
Protein Interaction databases
FunCoupENSG00000267638
BioGRIDLOC105371789
STRING (EMBL)LOC105371789
ZODIACLOC105371789
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease105371789
BioCentury BCIQLOC105371789
ClinGenLOC105371789
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD105371789
Clinical trialLOC105371789
Miscellaneous
canSAR (ICR)LOC105371789 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC105371789
EVEXLOC105371789
GoPubMedLOC105371789
iHOPLOC105371789
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Tue Nov 21 13:53:58 CET 2017

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