Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101927666 (uncharacterized LOC101927666)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927666
Atlas_Id 67192
Location 17q22  [Link to chromosome band 17q22]
Location_base_pair Starts at 58076891 and ends at 58083204 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)LOC101927666  101927666  uncharacterized LOC101927666
Aliases
GeneCards (Weizmann)LOC101927666
Ensembl hg19 (Hinxton)ENSG00000266290 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000266290 [Gene_View]  chr17:58076891-58083204 [Contig_View]  LOC101927666 [Vega]
ICGC DataPortalENSG00000266290
TCGA cBioPortalLOC101927666
AceView (NCBI)LOC101927666
Genatlas (Paris)LOC101927666
WikiGenes101927666
SOURCE (Princeton)LOC101927666
Genetics Home Reference (NIH)LOC101927666
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927666  -     chr17:58076891-58083204 -  17q22   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927666  -     17q22   [Description]    (hg19-Feb_2009)
EnsemblLOC101927666 - 17q22 [CytoView hg19]  LOC101927666 - 17q22 [CytoView hg38]
Mapping of homologs : NCBILOC101927666 [Mapview hg19]  LOC101927666 [Mapview hg38]
Gene and transcription
Genbank (Entrez)CR936603
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927666
Cluster EST : UnigeneHs.552237 [ NCBI ]
CGAP (NCI)Hs.552237
Alternative Splicing GalleryENSG00000266290
Gene ExpressionLOC101927666 [ NCBI-GEO ]   LOC101927666 [ EBI - ARRAY_EXPRESS ]   LOC101927666 [ SEEK ]   LOC101927666 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927666 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927666
GTEX Portal (Tissue expression)LOC101927666
Human Protein AtlasENSG00000266290-LOC101927666 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927666
DMDM Disease mutations101927666
Blocks (Seattle)LOC101927666
Human Protein Atlas [tissue]ENSG00000266290-LOC101927666 [tissue]
Protein Interaction databases
FunCoupENSG00000266290
BioGRIDLOC101927666
STRING (EMBL)LOC101927666
ZODIACLOC101927666
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927666
BioCentury BCIQLOC101927666
ClinGenLOC101927666
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927666
Clinical trialLOC101927666
Miscellaneous
canSAR (ICR)LOC101927666 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927666
EVEXLOC101927666
GoPubMedLOC101927666
iHOPLOC101927666
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 12:03:31 CET 2017

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