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LOC101927987 (uncharacterized LOC101927987)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927987
Atlas_Id 67260
Location 2p12  [Link to chromosome band 2p12]
Location_base_pair Starts at 79493716 and ends at 79500844 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)LOC101927987  101927987  uncharacterized LOC101927987
Aliases
GeneCards (Weizmann)LOC101927987
Ensembl hg19 (Hinxton)ENSG00000229385 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000229385 [Gene_View]  chr2:79493716-79500844 [Contig_View]  LOC101927987 [Vega]
ICGC DataPortalENSG00000229385
TCGA cBioPortalLOC101927987
AceView (NCBI)LOC101927987
Genatlas (Paris)LOC101927987
WikiGenes101927987
SOURCE (Princeton)LOC101927987
Genetics Home Reference (NIH)LOC101927987
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927987  -     chr2:79493716-79500844 -  2p12   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927987  -     2p12   [Description]    (hg19-Feb_2009)
EnsemblLOC101927987 - 2p12 [CytoView hg19]  LOC101927987 - 2p12 [CytoView hg38]
Mapping of homologs : NCBILOC101927987 [Mapview hg19]  LOC101927987 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AL709875
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927987
Cluster EST : UnigeneHs.574704 [ NCBI ]
CGAP (NCI)Hs.574704
Alternative Splicing GalleryENSG00000229385
Gene ExpressionLOC101927987 [ NCBI-GEO ]   LOC101927987 [ EBI - ARRAY_EXPRESS ]   LOC101927987 [ SEEK ]   LOC101927987 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927987 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927987
GTEX Portal (Tissue expression)LOC101927987
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927987
DMDM Disease mutations101927987
Blocks (Seattle)LOC101927987
Human Protein AtlasENSG00000229385
Protein Interaction databases
FunCoupENSG00000229385
BioGRIDLOC101927987
STRING (EMBL)LOC101927987
ZODIACLOC101927987
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927987
BioCentury BCIQLOC101927987
ClinGenLOC101927987
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927987
Clinical trialLOC101927987
Miscellaneous
canSAR (ICR)LOC101927987 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927987
EVEXLOC101927987
GoPubMedLOC101927987
iHOPLOC101927987
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 16:04:47 CEST 2017

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