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LOC101929762 (uncharacterized LOC101929762)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929762
Atlas_Id 67632
Location 4q26  [Link to chromosome band 4q26]
Location_base_pair Starts at 119192773 and ends at 119212644 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

RefSeq transcript (Entrez)
Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)LOC101929762  101929762  uncharacterized LOC101929762
Aliases
GeneCards (Weizmann)LOC101929762
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr4:119192773-119212644 [Contig_View]  LOC101929762 [Vega]
TCGA cBioPortalLOC101929762
AceView (NCBI)LOC101929762
Genatlas (Paris)LOC101929762
WikiGenes101929762
SOURCE (Princeton)LOC101929762
Genetics Home Reference (NIH)LOC101929762
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929762  -     chr4:119192773-119212644 -  4q26   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929762  -     4q26   [Description]    (hg19-Feb_2009)
EnsemblLOC101929762 - 4q26 [CytoView hg19]  LOC101929762 - 4q26 [CytoView hg38]
Mapping of homologs : NCBILOC101929762 [Mapview hg19]  LOC101929762 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK098126 AK309988
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929762
Cluster EST : UnigeneHs.570735 [ NCBI ]
CGAP (NCI)Hs.570735
Gene ExpressionLOC101929762 [ NCBI-GEO ]   LOC101929762 [ EBI - ARRAY_EXPRESS ]   LOC101929762 [ SEEK ]   LOC101929762 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929762 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929762
GTEX Portal (Tissue expression)LOC101929762
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929762
DMDM Disease mutations101929762
Blocks (Seattle)LOC101929762
Protein Interaction databases
BioGRIDLOC101929762
STRING (EMBL)LOC101929762
ZODIACLOC101929762
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929762
BioCentury BCIQLOC101929762
ClinGenLOC101929762
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929762
Clinical trialLOC101929762
Miscellaneous
canSAR (ICR)LOC101929762 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929762
EVEXLOC101929762
GoPubMedLOC101929762
iHOPLOC101929762
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 13:52:28 CET 2017

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