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LOC101929552 (uncharacterized LOC101929552)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929552
Atlas_Id 78369
Location 17q25.3  [Link to chromosome band 17q25]
Location_base_pair Starts at 82713908 and ends at 82716253 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)LOC101929552  101929552  uncharacterized LOC101929552
Aliases
GeneCards (Weizmann)LOC101929552
Ensembl hg19 (Hinxton)ENSG00000263063 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000263063 [Gene_View]  chr17:82713908-82716253 [Contig_View]  LOC101929552 [Vega]
ICGC DataPortalENSG00000263063
TCGA cBioPortalLOC101929552
AceView (NCBI)LOC101929552
Genatlas (Paris)LOC101929552
WikiGenes101929552
SOURCE (Princeton)LOC101929552
Genetics Home Reference (NIH)LOC101929552
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929552  -     chr17:82713908-82716253 -  17q25.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929552  -     17q25.3   [Description]    (hg19-Feb_2009)
EnsemblLOC101929552 - 17q25.3 [CytoView hg19]  LOC101929552 - 17q25.3 [CytoView hg38]
Mapping of homologs : NCBILOC101929552 [Mapview hg19]  LOC101929552 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC033940
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929552
Cluster EST : UnigeneHs.375081 [ NCBI ]
CGAP (NCI)Hs.375081
Alternative Splicing GalleryENSG00000263063
Gene ExpressionLOC101929552 [ NCBI-GEO ]   LOC101929552 [ EBI - ARRAY_EXPRESS ]   LOC101929552 [ SEEK ]   LOC101929552 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929552 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929552
GTEX Portal (Tissue expression)LOC101929552
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929552
DMDM Disease mutations101929552
Blocks (Seattle)LOC101929552
Human Protein AtlasENSG00000263063
Protein Interaction databases
FunCoupENSG00000263063
BioGRIDLOC101929552
STRING (EMBL)LOC101929552
ZODIACLOC101929552
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929552
BioCentury BCIQLOC101929552
ClinGenLOC101929552
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929552
Clinical trialLOC101929552
Miscellaneous
canSAR (ICR)LOC101929552 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929552
EVEXLOC101929552
GoPubMedLOC101929552
iHOPLOC101929552
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 : Mon Sep 18 13:21:47 CEST 2017

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