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LOC101060553 (uncharacterized LOC101060553)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101060553
Atlas_Id 66996
Location 13q34  [Link to chromosome band 13q34]
Location_base_pair Starts at 111148197 and ends at 111153577 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)LOC101060553  101060553  uncharacterized LOC101060553
Aliases
GeneCards (Weizmann)LOC101060553
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr13:111148197-111153577 [Contig_View]  LOC101060553 [Vega]
TCGA cBioPortalLOC101060553
AceView (NCBI)LOC101060553
Genatlas (Paris)LOC101060553
WikiGenes101060553
SOURCE (Princeton)LOC101060553
Genetics Home Reference (NIH)LOC101060553
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101060553  -     chr13:111148197-111153577 -  13q34   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101060553  -     13q34   [Description]    (hg19-Feb_2009)
EnsemblLOC101060553 - 13q34 [CytoView hg19]  LOC101060553 - 13q34 [CytoView hg38]
Mapping of homologs : NCBILOC101060553 [Mapview hg19]  LOC101060553 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC041861
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101060553
Cluster EST : UnigeneHs.662213 [ NCBI ]
CGAP (NCI)Hs.662213
Gene ExpressionLOC101060553 [ NCBI-GEO ]   LOC101060553 [ EBI - ARRAY_EXPRESS ]   LOC101060553 [ SEEK ]   LOC101060553 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101060553 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101060553
GTEX Portal (Tissue expression)LOC101060553
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101060553
DMDM Disease mutations101060553
Blocks (Seattle)LOC101060553
Protein Interaction databases
BioGRIDLOC101060553
STRING (EMBL)LOC101060553
ZODIACLOC101060553
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101060553
BioCentury BCIQLOC101060553
ClinGenLOC101060553
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101060553
Clinical trialLOC101060553
Miscellaneous
canSAR (ICR)LOC101060553 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101060553
EVEXLOC101060553
GoPubMedLOC101060553
iHOPLOC101060553
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 13:49:28 CET 2017

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