Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC105371899 (uncharacterized LOC105371899)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 105371899
Atlas_Id 78485
Location 17q25.2  [Link to chromosome band 17q25]
Location_base_pair Starts at 76962746 and ends at 76969199 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)LOC105371899  105371899  uncharacterized LOC105371899
Aliases
GeneCards (Weizmann)LOC105371899
Ensembl hg19 (Hinxton)ENSG00000267568 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000267568 [Gene_View]  chr17:76962746-76969199 [Contig_View]  LOC105371899 [Vega]
ICGC DataPortalENSG00000267568
TCGA cBioPortalLOC105371899
AceView (NCBI)LOC105371899
Genatlas (Paris)LOC105371899
WikiGenes105371899
SOURCE (Princeton)LOC105371899
Genetics Home Reference (NIH)LOC105371899
Genomic and cartography
GoldenPath hg38 (UCSC)LOC105371899  -     chr17:76962746-76969199 -  17q25.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC105371899  -     17q25.2   [Description]    (hg19-Feb_2009)
EnsemblLOC105371899 - 17q25.2 [CytoView hg19]  LOC105371899 - 17q25.2 [CytoView hg38]
Mapping of homologs : NCBILOC105371899 [Mapview hg19]  LOC105371899 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BM700476 CD173460 CD675441 CD675892 DB157978
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC105371899
Cluster EST : UnigeneHs.637824 [ NCBI ]
CGAP (NCI)Hs.637824
Alternative Splicing GalleryENSG00000267568
Gene ExpressionLOC105371899 [ NCBI-GEO ]   LOC105371899 [ EBI - ARRAY_EXPRESS ]   LOC105371899 [ SEEK ]   LOC105371899 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC105371899 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)105371899
GTEX Portal (Tissue expression)LOC105371899
Human Protein AtlasENSG00000267568-LOC105371899 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC105371899
DMDM Disease mutations105371899
Blocks (Seattle)LOC105371899
Human Protein Atlas [tissue]ENSG00000267568-LOC105371899 [tissue]
Protein Interaction databases
FunCoupENSG00000267568
BioGRIDLOC105371899
STRING (EMBL)LOC105371899
ZODIACLOC105371899
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease105371899
BioCentury BCIQLOC105371899
ClinGenLOC105371899
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD105371899
Clinical trialLOC105371899
Miscellaneous
canSAR (ICR)LOC105371899 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC105371899
EVEXLOC105371899
GoPubMedLOC105371899
iHOPLOC105371899
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 : Thu Nov 9 12:07:08 CET 2017

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