Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101927018 (uncharacterized LOC101927018)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927018
Atlas_Id 67031
Location 17q11.2  [Link to chromosome band 17q11]
Location_base_pair Starts at 28926275 and ends at 28944748 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)LOC101927018  101927018  uncharacterized LOC101927018
Aliases
GeneCards (Weizmann)LOC101927018
Ensembl hg19 (Hinxton)ENSG00000265845 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000265845 [Gene_View]  chr17:28926275-28944748 [Contig_View]  LOC101927018 [Vega]
ICGC DataPortalENSG00000265845
TCGA cBioPortalLOC101927018
AceView (NCBI)LOC101927018
Genatlas (Paris)LOC101927018
WikiGenes101927018
SOURCE (Princeton)LOC101927018
Genetics Home Reference (NIH)LOC101927018
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927018  -     chr17:28926275-28944748 +  17q11.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927018  -     17q11.2   [Description]    (hg19-Feb_2009)
EnsemblLOC101927018 - 17q11.2 [CytoView hg19]  LOC101927018 - 17q11.2 [CytoView hg38]
Mapping of homologs : NCBILOC101927018 [Mapview hg19]  LOC101927018 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC033997
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927018
Cluster EST : UnigeneHs.665702 [ NCBI ]
CGAP (NCI)Hs.665702
Alternative Splicing GalleryENSG00000265845
Gene ExpressionLOC101927018 [ NCBI-GEO ]   LOC101927018 [ EBI - ARRAY_EXPRESS ]   LOC101927018 [ SEEK ]   LOC101927018 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927018 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927018
GTEX Portal (Tissue expression)LOC101927018
Human Protein AtlasENSG00000265845-LOC101927018 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927018
DMDM Disease mutations101927018
Blocks (Seattle)LOC101927018
Human Protein Atlas [tissue]ENSG00000265845-LOC101927018 [tissue]
Protein Interaction databases
FunCoupENSG00000265845
BioGRIDLOC101927018
STRING (EMBL)LOC101927018
ZODIACLOC101927018
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927018
BioCentury BCIQLOC101927018
ClinGenLOC101927018
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927018
Clinical trialLOC101927018
Miscellaneous
canSAR (ICR)LOC101927018 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927018
EVEXLOC101927018
GoPubMedLOC101927018
iHOPLOC101927018
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 : Thu Nov 9 12:02:49 CET 2017

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