Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101927780 (uncharacterized LOC101927780)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927780
Atlas_Id 67213
Location 14q23.1  [Link to chromosome band 14q23]
Location_base_pair Starts at 61556272 and ends at 61570653 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)

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)LOC101927780  101927780  uncharacterized LOC101927780
Aliases
GeneCards (Weizmann)LOC101927780
Ensembl hg19 (Hinxton)ENSG00000250548 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000250548 [Gene_View]  chr14:61556272-61570653 [Contig_View]  LOC101927780 [Vega]
ICGC DataPortalENSG00000250548
TCGA cBioPortalLOC101927780
AceView (NCBI)LOC101927780
Genatlas (Paris)LOC101927780
WikiGenes101927780
SOURCE (Princeton)LOC101927780
Genetics Home Reference (NIH)LOC101927780
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927780  -     chr14:61556272-61570653 -  14q23.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927780  -     14q23.1   [Description]    (hg19-Feb_2009)
EnsemblLOC101927780 - 14q23.1 [CytoView hg19]  LOC101927780 - 14q23.1 [CytoView hg38]
Mapping of homologs : NCBILOC101927780 [Mapview hg19]  LOC101927780 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AW275370 BX648502 HY039622
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927780
Cluster EST : UnigeneHs.254789 [ NCBI ]
CGAP (NCI)Hs.254789
Alternative Splicing GalleryENSG00000250548
Gene ExpressionLOC101927780 [ NCBI-GEO ]   LOC101927780 [ EBI - ARRAY_EXPRESS ]   LOC101927780 [ SEEK ]   LOC101927780 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927780 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927780
GTEX Portal (Tissue expression)LOC101927780
Human Protein AtlasENSG00000250548-LOC101927780 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927780
DMDM Disease mutations101927780
Blocks (Seattle)LOC101927780
Human Protein Atlas [tissue]ENSG00000250548-LOC101927780 [tissue]
Protein Interaction databases
FunCoupENSG00000250548
BioGRIDLOC101927780
STRING (EMBL)LOC101927780
ZODIACLOC101927780
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927780
BioCentury BCIQLOC101927780
ClinGenLOC101927780
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927780
Clinical trialLOC101927780
Miscellaneous
canSAR (ICR)LOC101927780 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927780
EVEXLOC101927780
GoPubMedLOC101927780
iHOPLOC101927780
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 : Tue Nov 21 13:50:27 CET 2017

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