Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101927402 (uncharacterized LOC101927402)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927402
Atlas_Id 78529
Location 2p14  [Link to chromosome band 2p14]
Location_base_pair Starts at 64522189 and ends at 64524155 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)LOC101927402  101927402  uncharacterized LOC101927402
Aliases
GeneCards (Weizmann)LOC101927402
Ensembl hg19 (Hinxton)ENSG00000260101 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000260101 [Gene_View]  chr2:64522189-64524155 [Contig_View]  LOC101927402 [Vega]
ICGC DataPortalENSG00000260101
TCGA cBioPortalLOC101927402
AceView (NCBI)LOC101927402
Genatlas (Paris)LOC101927402
WikiGenes101927402
SOURCE (Princeton)LOC101927402
Genetics Home Reference (NIH)LOC101927402
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927402  -     chr2:64522189-64524155 -  2p14   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927402  -     2p14   [Description]    (hg19-Feb_2009)
EnsemblLOC101927402 - 2p14 [CytoView hg19]  LOC101927402 - 2p14 [CytoView hg38]
Mapping of homologs : NCBILOC101927402 [Mapview hg19]  LOC101927402 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC035180
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927402
Cluster EST : UnigeneHs.187018 [ NCBI ]
CGAP (NCI)Hs.187018
Alternative Splicing GalleryENSG00000260101
Gene ExpressionLOC101927402 [ NCBI-GEO ]   LOC101927402 [ EBI - ARRAY_EXPRESS ]   LOC101927402 [ SEEK ]   LOC101927402 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927402 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927402
GTEX Portal (Tissue expression)LOC101927402
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927402
DMDM Disease mutations101927402
Blocks (Seattle)LOC101927402
Human Protein AtlasENSG00000260101
Protein Interaction databases
FunCoupENSG00000260101
BioGRIDLOC101927402
STRING (EMBL)LOC101927402
ZODIACLOC101927402
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927402
BioCentury BCIQLOC101927402
ClinGenLOC101927402
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927402
Clinical trialLOC101927402
Miscellaneous
canSAR (ICR)LOC101927402 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927402
EVEXLOC101927402
GoPubMedLOC101927402
iHOPLOC101927402
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 16:04:05 CEST 2017

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