Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101928674 (uncharacterized LOC101928674)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928674
Atlas_Id 67405
Location 17q25.3  [Link to chromosome band 17q25]
Location_base_pair Starts at 78360448 and ends at 78364931 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)LOC101928674  101928674  uncharacterized LOC101928674
Aliases
GeneCards (Weizmann)LOC101928674
Ensembl hg19 (Hinxton)ENSG00000266970 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000266970 [Gene_View]  chr17:78360448-78364931 [Contig_View]  LOC101928674 [Vega]
ICGC DataPortalENSG00000266970
TCGA cBioPortalLOC101928674
AceView (NCBI)LOC101928674
Genatlas (Paris)LOC101928674
WikiGenes101928674
SOURCE (Princeton)LOC101928674
Genetics Home Reference (NIH)LOC101928674
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101928674  -     chr17:78360448-78364931 +  17q25.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101928674  -     17q25.3   [Description]    (hg19-Feb_2009)
EnsemblLOC101928674 - 17q25.3 [CytoView hg19]  LOC101928674 - 17q25.3 [CytoView hg38]
Mapping of homologs : NCBILOC101928674 [Mapview hg19]  LOC101928674 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BG437436 HY169606 HY173789
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101928674
Cluster EST : UnigeneHs.637297 [ NCBI ]
CGAP (NCI)Hs.637297
Alternative Splicing GalleryENSG00000266970
Gene ExpressionLOC101928674 [ NCBI-GEO ]   LOC101928674 [ EBI - ARRAY_EXPRESS ]   LOC101928674 [ SEEK ]   LOC101928674 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928674 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928674
GTEX Portal (Tissue expression)LOC101928674
Human Protein AtlasENSG00000266970-LOC101928674 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928674
DMDM Disease mutations101928674
Blocks (Seattle)LOC101928674
Human Protein Atlas [tissue]ENSG00000266970-LOC101928674 [tissue]
Protein Interaction databases
FunCoupENSG00000266970
BioGRIDLOC101928674
STRING (EMBL)LOC101928674
ZODIACLOC101928674
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928674
BioCentury BCIQLOC101928674
ClinGenLOC101928674
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928674
Clinical trialLOC101928674
Miscellaneous
canSAR (ICR)LOC101928674 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101928674
EVEXLOC101928674
GoPubMedLOC101928674
iHOPLOC101928674
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 : Tue Nov 21 13:51:25 CET 2017

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