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LOC101927911 (uncharacterized LOC101927911)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927911
Atlas_Id 67245
Location 17p13.3  [Link to chromosome band 17p13]
Location_base_pair Starts at 2962247 and ends at 2965895 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)LOC101927911  101927911  uncharacterized LOC101927911
Aliases
GeneCards (Weizmann)LOC101927911
Ensembl hg19 (Hinxton)ENSG00000262884 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000262884 [Gene_View]  chr17:2962247-2965895 [Contig_View]  LOC101927911 [Vega]
ICGC DataPortalENSG00000262884
TCGA cBioPortalLOC101927911
AceView (NCBI)LOC101927911
Genatlas (Paris)LOC101927911
WikiGenes101927911
SOURCE (Princeton)LOC101927911
Genetics Home Reference (NIH)LOC101927911
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927911  -     chr17:2962247-2965895 -  17p13.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927911  -     17p13.3   [Description]    (hg19-Feb_2009)
EnsemblLOC101927911 - 17p13.3 [CytoView hg19]  LOC101927911 - 17p13.3 [CytoView hg38]
Mapping of homologs : NCBILOC101927911 [Mapview hg19]  LOC101927911 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC069263
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927911
Cluster EST : UnigeneHs.626373 [ NCBI ]
CGAP (NCI)Hs.626373
Alternative Splicing GalleryENSG00000262884
Gene ExpressionLOC101927911 [ NCBI-GEO ]   LOC101927911 [ EBI - ARRAY_EXPRESS ]   LOC101927911 [ SEEK ]   LOC101927911 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927911 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927911
GTEX Portal (Tissue expression)LOC101927911
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927911
DMDM Disease mutations101927911
Blocks (Seattle)LOC101927911
Human Protein AtlasENSG00000262884
Protein Interaction databases
FunCoupENSG00000262884
BioGRIDLOC101927911
STRING (EMBL)LOC101927911
ZODIACLOC101927911
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927911
BioCentury BCIQLOC101927911
ClinGenLOC101927911
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927911
Clinical trialLOC101927911
Miscellaneous
canSAR (ICR)LOC101927911 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927911
EVEXLOC101927911
GoPubMedLOC101927911
iHOPLOC101927911
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 : Wed Jun 7 16:04:42 CEST 2017

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