Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101928887 (uncharacterized LOC101928887)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928887
Atlas_Id 76803
Location 10q21.3  [Link to chromosome band 10q21]
Location_base_pair Starts at 64901136 and ends at 64924518 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)LOC101928887  101928887  uncharacterized LOC101928887
Aliases
GeneCards (Weizmann)LOC101928887
Ensembl hg19 (Hinxton)ENSG00000224714 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000224714 [Gene_View]  chr10:64901136-64924518 [Contig_View]  LOC101928887 [Vega]
ICGC DataPortalENSG00000224714
TCGA cBioPortalLOC101928887
AceView (NCBI)LOC101928887
Genatlas (Paris)LOC101928887
WikiGenes101928887
SOURCE (Princeton)LOC101928887
Genetics Home Reference (NIH)LOC101928887
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101928887  -     chr10:64901136-64924518 -  10q21.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101928887  -     10q21.3   [Description]    (hg19-Feb_2009)
EnsemblLOC101928887 - 10q21.3 [CytoView hg19]  LOC101928887 - 10q21.3 [CytoView hg38]
Mapping of homologs : NCBILOC101928887 [Mapview hg19]  LOC101928887 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC050028
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101928887
Cluster EST : UnigeneHs.463900 [ NCBI ]
CGAP (NCI)Hs.463900
Alternative Splicing GalleryENSG00000224714
Gene ExpressionLOC101928887 [ NCBI-GEO ]   LOC101928887 [ EBI - ARRAY_EXPRESS ]   LOC101928887 [ SEEK ]   LOC101928887 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928887 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928887
GTEX Portal (Tissue expression)LOC101928887
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928887
DMDM Disease mutations101928887
Blocks (Seattle)LOC101928887
Human Protein AtlasENSG00000224714
Protein Interaction databases
FunCoupENSG00000224714
BioGRIDLOC101928887
STRING (EMBL)LOC101928887
ZODIACLOC101928887
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928887
BioCentury BCIQLOC101928887
ClinGenLOC101928887
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928887
Clinical trialLOC101928887
Miscellaneous
canSAR (ICR)LOC101928887 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101928887
EVEXLOC101928887
GoPubMedLOC101928887
iHOPLOC101928887
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 : Wed Jun 7 16:05:49 CEST 2017

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