Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101927877 (uncharacterized LOC101927877)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927877
Atlas_Id 77295
Location 17q23.2  [Link to chromosome band 17q23]
Location_base_pair Starts at 62808502 and ends at 62836371 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)LOC101927877  101927877  uncharacterized LOC101927877
Aliases
GeneCards (Weizmann)LOC101927877
Ensembl hg19 (Hinxton)ENSG00000265000 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000265000 [Gene_View]  chr17:62808502-62836371 [Contig_View]  LOC101927877 [Vega]
ICGC DataPortalENSG00000265000
TCGA cBioPortalLOC101927877
AceView (NCBI)LOC101927877
Genatlas (Paris)LOC101927877
WikiGenes101927877
SOURCE (Princeton)LOC101927877
Genetics Home Reference (NIH)LOC101927877
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927877  -     chr17:62808502-62836371 +  17q23.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927877  -     17q23.2   [Description]    (hg19-Feb_2009)
EnsemblLOC101927877 - 17q23.2 [CytoView hg19]  LOC101927877 - 17q23.2 [CytoView hg38]
Mapping of homologs : NCBILOC101927877 [Mapview hg19]  LOC101927877 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC040294
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927877
Cluster EST : UnigeneHs.434615 [ NCBI ]
CGAP (NCI)Hs.434615
Alternative Splicing GalleryENSG00000265000
Gene ExpressionLOC101927877 [ NCBI-GEO ]   LOC101927877 [ EBI - ARRAY_EXPRESS ]   LOC101927877 [ SEEK ]   LOC101927877 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927877 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927877
GTEX Portal (Tissue expression)LOC101927877
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927877
DMDM Disease mutations101927877
Blocks (Seattle)LOC101927877
Human Protein AtlasENSG00000265000
Protein Interaction databases
FunCoupENSG00000265000
BioGRIDLOC101927877
STRING (EMBL)LOC101927877
ZODIACLOC101927877
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927877
BioCentury BCIQLOC101927877
ClinGenLOC101927877
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927877
Clinical trialLOC101927877
Miscellaneous
canSAR (ICR)LOC101927877 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927877
EVEXLOC101927877
GoPubMedLOC101927877
iHOPLOC101927877
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 16:04:39 CEST 2017

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