Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101927708 (uncharacterized LOC101927708)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927708
Atlas_Id 77047
Location 11p15.4  [Link to chromosome band 11p15]
Location_base_pair Starts at 3507980 and ends at 3571987 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)LOC101927708  101927708  uncharacterized LOC101927708
Aliases
GeneCards (Weizmann)LOC101927708
Ensembl hg19 (Hinxton)ENSG00000255367 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000255367 [Gene_View]  chr11:3507980-3571987 [Contig_View]  LOC101927708 [Vega]
ICGC DataPortalENSG00000255367
TCGA cBioPortalLOC101927708
AceView (NCBI)LOC101927708
Genatlas (Paris)LOC101927708
WikiGenes101927708
SOURCE (Princeton)LOC101927708
Genetics Home Reference (NIH)LOC101927708
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927708  -     chr11:3507980-3571987 -  11p15.4   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927708  -     11p15.4   [Description]    (hg19-Feb_2009)
EnsemblLOC101927708 - 11p15.4 [CytoView hg19]  LOC101927708 - 11p15.4 [CytoView hg38]
Mapping of homologs : NCBILOC101927708 [Mapview hg19]  LOC101927708 [Mapview hg38]
Gene and transcription
Genbank (Entrez)DB199773
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927708
Cluster EST : UnigeneHs.577316 [ NCBI ]
CGAP (NCI)Hs.577316
Alternative Splicing GalleryENSG00000255367
Gene ExpressionLOC101927708 [ NCBI-GEO ]   LOC101927708 [ EBI - ARRAY_EXPRESS ]   LOC101927708 [ SEEK ]   LOC101927708 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927708 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927708
GTEX Portal (Tissue expression)LOC101927708
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927708
DMDM Disease mutations101927708
Blocks (Seattle)LOC101927708
Human Protein AtlasENSG00000255367
Protein Interaction databases
FunCoupENSG00000255367
BioGRIDLOC101927708
STRING (EMBL)LOC101927708
ZODIACLOC101927708
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927708
BioCentury BCIQLOC101927708
ClinGenLOC101927708
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927708
Clinical trialLOC101927708
Miscellaneous
canSAR (ICR)LOC101927708 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927708
EVEXLOC101927708
GoPubMedLOC101927708
iHOPLOC101927708
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 16:04:28 CEST 2017

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