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LOC101929657 (uncharacterized LOC101929657)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929657
Atlas_Id 67608
Location 13q14.3  [Link to chromosome band 13q14]
Location_base_pair Starts at 52128895 and ends at 52132723 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)LOC101929657  101929657  uncharacterized LOC101929657
Aliases
GeneCards (Weizmann)LOC101929657
Ensembl hg19 (Hinxton)ENSG00000273523 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000273523 [Gene_View]  chr13:52128895-52132723 [Contig_View]  LOC101929657 [Vega]
ICGC DataPortalENSG00000273523
TCGA cBioPortalLOC101929657
AceView (NCBI)LOC101929657
Genatlas (Paris)LOC101929657
WikiGenes101929657
SOURCE (Princeton)LOC101929657
Genetics Home Reference (NIH)LOC101929657
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929657  -     chr13:52128895-52132723 +  13q14.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929657  -     13q14.3   [Description]    (hg19-Feb_2009)
EnsemblLOC101929657 - 13q14.3 [CytoView hg19]  LOC101929657 - 13q14.3 [CytoView hg38]
Mapping of homologs : NCBILOC101929657 [Mapview hg19]  LOC101929657 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC036321
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929657
Cluster EST : UnigeneHs.637461 [ NCBI ]
CGAP (NCI)Hs.637461
Alternative Splicing GalleryENSG00000273523
Gene ExpressionLOC101929657 [ NCBI-GEO ]   LOC101929657 [ EBI - ARRAY_EXPRESS ]   LOC101929657 [ SEEK ]   LOC101929657 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929657 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929657
GTEX Portal (Tissue expression)LOC101929657
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929657
DMDM Disease mutations101929657
Blocks (Seattle)LOC101929657
Human Protein AtlasENSG00000273523
Protein Interaction databases
FunCoupENSG00000273523
BioGRIDLOC101929657
STRING (EMBL)LOC101929657
ZODIACLOC101929657
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929657
BioCentury BCIQLOC101929657
ClinGenLOC101929657
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929657
Clinical trialLOC101929657
Miscellaneous
canSAR (ICR)LOC101929657 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929657
EVEXLOC101929657
GoPubMedLOC101929657
iHOPLOC101929657
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 13:21:52 CEST 2017

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