Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101927755 (uncharacterized LOC101927755)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927755
Atlas_Id 67206
Location 17q23.1  [Link to chromosome band 17q23]
Location_base_pair Starts at 59965096 and ends at 59996972 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)LOC101927755  101927755  uncharacterized LOC101927755
Aliases
GeneCards (Weizmann)LOC101927755
Ensembl hg19 (Hinxton)ENSG00000267302 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000267302 [Gene_View]  chr17:59965096-59996972 [Contig_View]  LOC101927755 [Vega]
ICGC DataPortalENSG00000267302
TCGA cBioPortalLOC101927755
AceView (NCBI)LOC101927755
Genatlas (Paris)LOC101927755
WikiGenes101927755
SOURCE (Princeton)LOC101927755
Genetics Home Reference (NIH)LOC101927755
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927755  -     chr17:59965096-59996972 +  17q23.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927755  -     17q23.1   [Description]    (hg19-Feb_2009)
EnsemblLOC101927755 - 17q23.1 [CytoView hg19]  LOC101927755 - 17q23.1 [CytoView hg38]
Mapping of homologs : NCBILOC101927755 [Mapview hg19]  LOC101927755 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AI792936 AK097658 BF002978
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927755
Cluster EST : UnigeneHs.733307 [ NCBI ]
CGAP (NCI)Hs.733307
Alternative Splicing GalleryENSG00000267302
Gene ExpressionLOC101927755 [ NCBI-GEO ]   LOC101927755 [ EBI - ARRAY_EXPRESS ]   LOC101927755 [ SEEK ]   LOC101927755 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927755 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927755
GTEX Portal (Tissue expression)LOC101927755
Human Protein AtlasENSG00000267302-LOC101927755 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927755
DMDM Disease mutations101927755
Blocks (Seattle)LOC101927755
Human Protein Atlas [tissue]ENSG00000267302-LOC101927755 [tissue]
Protein Interaction databases
FunCoupENSG00000267302
BioGRIDLOC101927755
STRING (EMBL)LOC101927755
ZODIACLOC101927755
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927755
BioCentury BCIQLOC101927755
ClinGenLOC101927755
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927755
Clinical trialLOC101927755
Miscellaneous
canSAR (ICR)LOC101927755 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927755
EVEXLOC101927755
GoPubMedLOC101927755
iHOPLOC101927755
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 12:03:35 CET 2017

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