Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101928443 (uncharacterized LOC101928443)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928443
Atlas_Id 67356
Location 11q13.3  [Link to chromosome band 11q13]
Location_base_pair Starts at 70056230 and ends at 70065371 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)LOC101928443  101928443  uncharacterized LOC101928443
Aliases
GeneCards (Weizmann)LOC101928443
Ensembl hg19 (Hinxton)ENSG00000248844 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000248844 [Gene_View]  chr11:70056230-70065371 [Contig_View]  LOC101928443 [Vega]
ICGC DataPortalENSG00000248844
TCGA cBioPortalLOC101928443
AceView (NCBI)LOC101928443
Genatlas (Paris)LOC101928443
WikiGenes101928443
SOURCE (Princeton)LOC101928443
Genetics Home Reference (NIH)LOC101928443
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101928443  -     chr11:70056230-70065371 -  11q13.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101928443  -     11q13.3   [Description]    (hg19-Feb_2009)
EnsemblLOC101928443 - 11q13.3 [CytoView hg19]  LOC101928443 - 11q13.3 [CytoView hg38]
Mapping of homologs : NCBILOC101928443 [Mapview hg19]  LOC101928443 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AW340489 BC039105
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101928443
Cluster EST : UnigeneHs.639242 [ NCBI ]
CGAP (NCI)Hs.639242
Alternative Splicing GalleryENSG00000248844
Gene ExpressionLOC101928443 [ NCBI-GEO ]   LOC101928443 [ EBI - ARRAY_EXPRESS ]   LOC101928443 [ SEEK ]   LOC101928443 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928443 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928443
GTEX Portal (Tissue expression)LOC101928443
Human Protein AtlasENSG00000248844-LOC101928443 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928443
DMDM Disease mutations101928443
Blocks (Seattle)LOC101928443
Human Protein Atlas [tissue]ENSG00000248844-LOC101928443 [tissue]
Protein Interaction databases
FunCoupENSG00000248844
BioGRIDLOC101928443
STRING (EMBL)LOC101928443
ZODIACLOC101928443
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928443
BioCentury BCIQLOC101928443
ClinGenLOC101928443
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928443
Clinical trialLOC101928443
Miscellaneous
canSAR (ICR)LOC101928443 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101928443
EVEXLOC101928443
GoPubMedLOC101928443
iHOPLOC101928443
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Thu Nov 9 12:04:21 CET 2017

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