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LOC101928132 (uncharacterized LOC101928132)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928132
Atlas_Id 77041
Location 11p15.2  [Link to chromosome band 11p15]
Location_base_pair Starts at 13921447 and ends at 13924863 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)LOC101928132  101928132  uncharacterized LOC101928132
Aliases
GeneCards (Weizmann)LOC101928132
Ensembl hg19 (Hinxton)ENSG00000254438 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000254438 [Gene_View]  chr11:13921447-13924863 [Contig_View]  LOC101928132 [Vega]
ICGC DataPortalENSG00000254438
TCGA cBioPortalLOC101928132
AceView (NCBI)LOC101928132
Genatlas (Paris)LOC101928132
WikiGenes101928132
SOURCE (Princeton)LOC101928132
Genetics Home Reference (NIH)LOC101928132
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101928132  -     chr11:13921447-13924863 -  11p15.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101928132  -     11p15.2   [Description]    (hg19-Feb_2009)
EnsemblLOC101928132 - 11p15.2 [CytoView hg19]  LOC101928132 - 11p15.2 [CytoView hg38]
Mapping of homologs : NCBILOC101928132 [Mapview hg19]  LOC101928132 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AW025135 BC015849
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101928132
Cluster EST : UnigeneHs.568970 [ NCBI ]
CGAP (NCI)Hs.568970
Alternative Splicing GalleryENSG00000254438
Gene ExpressionLOC101928132 [ NCBI-GEO ]   LOC101928132 [ EBI - ARRAY_EXPRESS ]   LOC101928132 [ SEEK ]   LOC101928132 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928132 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928132
GTEX Portal (Tissue expression)LOC101928132
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928132
DMDM Disease mutations101928132
Blocks (Seattle)LOC101928132
Human Protein AtlasENSG00000254438
Protein Interaction databases
FunCoupENSG00000254438
BioGRIDLOC101928132
STRING (EMBL)LOC101928132
ZODIACLOC101928132
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928132
BioCentury BCIQLOC101928132
ClinGenLOC101928132
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928132
Clinical trialLOC101928132
Miscellaneous
canSAR (ICR)LOC101928132 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101928132
EVEXLOC101928132
GoPubMedLOC101928132
iHOPLOC101928132
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 : Fri May 19 11:28:58 CEST 2017

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