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LOC101927131 (uncharacterized LOC101927131)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927131
Atlas_Id 67060
Location 16p13.13  [Link to chromosome band 16p13]
Location_base_pair Starts at 11465260 and ends at 11473174 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)LOC101927131  101927131  uncharacterized LOC101927131
Aliases
GeneCards (Weizmann)LOC101927131
Ensembl hg19 (Hinxton)ENSG00000262999 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000262999 [Gene_View]  chr16:11465260-11473174 [Contig_View]  LOC101927131 [Vega]
ICGC DataPortalENSG00000262999
TCGA cBioPortalLOC101927131
AceView (NCBI)LOC101927131
Genatlas (Paris)LOC101927131
WikiGenes101927131
SOURCE (Princeton)LOC101927131
Genetics Home Reference (NIH)LOC101927131
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927131  -     chr16:11465260-11473174 +  16p13.13   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927131  -     16p13.13   [Description]    (hg19-Feb_2009)
EnsemblLOC101927131 - 16p13.13 [CytoView hg19]  LOC101927131 - 16p13.13 [CytoView hg38]
Mapping of homologs : NCBILOC101927131 [Mapview hg19]  LOC101927131 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC035158
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927131
Cluster EST : UnigeneHs.569654 [ NCBI ]
CGAP (NCI)Hs.569654
Alternative Splicing GalleryENSG00000262999
Gene ExpressionLOC101927131 [ NCBI-GEO ]   LOC101927131 [ EBI - ARRAY_EXPRESS ]   LOC101927131 [ SEEK ]   LOC101927131 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927131 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927131
GTEX Portal (Tissue expression)LOC101927131
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927131
DMDM Disease mutations101927131
Blocks (Seattle)LOC101927131
Human Protein AtlasENSG00000262999
Protein Interaction databases
FunCoupENSG00000262999
BioGRIDLOC101927131
STRING (EMBL)LOC101927131
ZODIACLOC101927131
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927131
BioCentury BCIQLOC101927131
ClinGenLOC101927131
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927131
Clinical trialLOC101927131
Miscellaneous
canSAR (ICR)LOC101927131 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927131
EVEXLOC101927131
GoPubMedLOC101927131
iHOPLOC101927131
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Fri May 19 11:27:47 CEST 2017

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