Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101929123 (uncharacterized LOC101929123)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929123
Atlas_Id 67495
Location 4p15.32  [Link to chromosome band 4p15]
Location_base_pair Starts at 17171757 and ends at 17186057 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)LOC101929123  101929123  uncharacterized LOC101929123
Aliases
GeneCards (Weizmann)LOC101929123
Ensembl hg19 (Hinxton)ENSG00000250819 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000250819 [Gene_View]  chr4:17171757-17186057 [Contig_View]  LOC101929123 [Vega]
ICGC DataPortalENSG00000250819
TCGA cBioPortalLOC101929123
AceView (NCBI)LOC101929123
Genatlas (Paris)LOC101929123
WikiGenes101929123
SOURCE (Princeton)LOC101929123
Genetics Home Reference (NIH)LOC101929123
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929123  -     chr4:17171757-17186057 -  4p15.32   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929123  -     4p15.32   [Description]    (hg19-Feb_2009)
EnsemblLOC101929123 - 4p15.32 [CytoView hg19]  LOC101929123 - 4p15.32 [CytoView hg38]
Mapping of homologs : NCBILOC101929123 [Mapview hg19]  LOC101929123 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC029598
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929123
Cluster EST : UnigeneHs.638913 [ NCBI ]
CGAP (NCI)Hs.638913
Alternative Splicing GalleryENSG00000250819
Gene ExpressionLOC101929123 [ NCBI-GEO ]   LOC101929123 [ EBI - ARRAY_EXPRESS ]   LOC101929123 [ SEEK ]   LOC101929123 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929123 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929123
GTEX Portal (Tissue expression)LOC101929123
Human Protein AtlasENSG00000250819-LOC101929123 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929123
DMDM Disease mutations101929123
Blocks (Seattle)LOC101929123
Human Protein Atlas [tissue]ENSG00000250819-LOC101929123 [tissue]
Protein Interaction databases
FunCoupENSG00000250819
BioGRIDLOC101929123
STRING (EMBL)LOC101929123
ZODIACLOC101929123
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929123
BioCentury BCIQLOC101929123
ClinGenLOC101929123
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929123
Clinical trialLOC101929123
Miscellaneous
canSAR (ICR)LOC101929123 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929123
EVEXLOC101929123
GoPubMedLOC101929123
iHOPLOC101929123
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 : Thu Nov 9 12:05:00 CET 2017

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