Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101929413 (uncharacterized LOC101929413)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929413
Atlas_Id 67550
Location 20p12.2  [Link to chromosome band 20p12]
Location_base_pair Starts at 10875333 and ends at 10909272 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)LOC101929413  101929413  uncharacterized LOC101929413
Aliases
GeneCards (Weizmann)LOC101929413
Ensembl hg19 (Hinxton)ENSG00000232900 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000232900 [Gene_View]  chr20:10875333-10909272 [Contig_View]  LOC101929413 [Vega]
ICGC DataPortalENSG00000232900
TCGA cBioPortalLOC101929413
AceView (NCBI)LOC101929413
Genatlas (Paris)LOC101929413
WikiGenes101929413
SOURCE (Princeton)LOC101929413
Genetics Home Reference (NIH)LOC101929413
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929413  -     chr20:10875333-10909272 -  20p12.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929413  -     20p12.2   [Description]    (hg19-Feb_2009)
EnsemblLOC101929413 - 20p12.2 [CytoView hg19]  LOC101929413 - 20p12.2 [CytoView hg38]
Mapping of homologs : NCBILOC101929413 [Mapview hg19]  LOC101929413 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC033557
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929413
Cluster EST : UnigeneHs.385604 [ NCBI ]
CGAP (NCI)Hs.385604
Alternative Splicing GalleryENSG00000232900
Gene ExpressionLOC101929413 [ NCBI-GEO ]   LOC101929413 [ EBI - ARRAY_EXPRESS ]   LOC101929413 [ SEEK ]   LOC101929413 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929413 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929413
GTEX Portal (Tissue expression)LOC101929413
Human Protein AtlasENSG00000232900-LOC101929413 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929413
DMDM Disease mutations101929413
Blocks (Seattle)LOC101929413
Human Protein Atlas [tissue]ENSG00000232900-LOC101929413 [tissue]
Protein Interaction databases
FunCoupENSG00000232900
BioGRIDLOC101929413
STRING (EMBL)LOC101929413
ZODIACLOC101929413
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929413
BioCentury BCIQLOC101929413
ClinGenLOC101929413
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929413
Clinical trialLOC101929413
Miscellaneous
canSAR (ICR)LOC101929413 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929413
EVEXLOC101929413
GoPubMedLOC101929413
iHOPLOC101929413
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 : Tue Nov 21 13:52:07 CET 2017

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