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LOC101927661 (uncharacterized LOC101927661)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927661
Atlas_Id 67191
Location 2p14  [Link to chromosome band 2p14]
Location_base_pair Starts at 67213408 and ends at 67244574 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)LOC101927661  101927661  uncharacterized LOC101927661
Aliases
GeneCards (Weizmann)LOC101927661
Ensembl hg19 (Hinxton)ENSG00000235885 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000235885 [Gene_View]  chr2:67213408-67244574 [Contig_View]  LOC101927661 [Vega]
ICGC DataPortalENSG00000235885
TCGA cBioPortalLOC101927661
AceView (NCBI)LOC101927661
Genatlas (Paris)LOC101927661
WikiGenes101927661
SOURCE (Princeton)LOC101927661
Genetics Home Reference (NIH)LOC101927661
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927661  -     chr2:67213408-67244574 +  2p14   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927661  -     2p14   [Description]    (hg19-Feb_2009)
EnsemblLOC101927661 - 2p14 [CytoView hg19]  LOC101927661 - 2p14 [CytoView hg38]
Mapping of homologs : NCBILOC101927661 [Mapview hg19]  LOC101927661 [Mapview hg38]
Gene and transcription
Genbank (Entrez)DA606408
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927661
Cluster EST : UnigeneHs.580508 [ NCBI ]
CGAP (NCI)Hs.580508
Alternative Splicing GalleryENSG00000235885
Gene ExpressionLOC101927661 [ NCBI-GEO ]   LOC101927661 [ EBI - ARRAY_EXPRESS ]   LOC101927661 [ SEEK ]   LOC101927661 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927661 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927661
GTEX Portal (Tissue expression)LOC101927661
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927661
DMDM Disease mutations101927661
Blocks (Seattle)LOC101927661
Human Protein AtlasENSG00000235885
Protein Interaction databases
FunCoupENSG00000235885
BioGRIDLOC101927661
STRING (EMBL)LOC101927661
ZODIACLOC101927661
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927661
BioCentury BCIQLOC101927661
ClinGenLOC101927661
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927661
Clinical trialLOC101927661
Miscellaneous
canSAR (ICR)LOC101927661 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927661
EVEXLOC101927661
GoPubMedLOC101927661
iHOPLOC101927661
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 16:04:25 CEST 2017

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