Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101929315 (uncharacterized LOC101929315)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929315
Atlas_Id 67534
Location 8p21.2  [Link to chromosome band 8p21]
Location_base_pair Starts at 24490312 and ends at 24514868 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)LOC101929315  101929315  uncharacterized LOC101929315
Aliases
GeneCards (Weizmann)LOC101929315
Ensembl hg19 (Hinxton)ENSG00000253643 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000253643 [Gene_View]  chr8:24490312-24514868 [Contig_View]  LOC101929315 [Vega]
ICGC DataPortalENSG00000253643
TCGA cBioPortalLOC101929315
AceView (NCBI)LOC101929315
Genatlas (Paris)LOC101929315
WikiGenes101929315
SOURCE (Princeton)LOC101929315
Genetics Home Reference (NIH)LOC101929315
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929315  -     chr8:24490312-24514868 -  8p21.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929315  -     8p21.2   [Description]    (hg19-Feb_2009)
EnsemblLOC101929315 - 8p21.2 [CytoView hg19]  LOC101929315 - 8p21.2 [CytoView hg38]
Mapping of homologs : NCBILOC101929315 [Mapview hg19]  LOC101929315 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AA724983 AI125340 AI208246 AI221180 BX096372
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929315
Cluster EST : UnigeneHs.571452 [ NCBI ]
CGAP (NCI)Hs.571452
Alternative Splicing GalleryENSG00000253643
Gene ExpressionLOC101929315 [ NCBI-GEO ]   LOC101929315 [ EBI - ARRAY_EXPRESS ]   LOC101929315 [ SEEK ]   LOC101929315 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929315 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929315
GTEX Portal (Tissue expression)LOC101929315
Human Protein AtlasENSG00000253643-LOC101929315 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929315
DMDM Disease mutations101929315
Blocks (Seattle)LOC101929315
Human Protein Atlas [tissue]ENSG00000253643-LOC101929315 [tissue]
Protein Interaction databases
FunCoupENSG00000253643
BioGRIDLOC101929315
STRING (EMBL)LOC101929315
ZODIACLOC101929315
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929315
BioCentury BCIQLOC101929315
ClinGenLOC101929315
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929315
Clinical trialLOC101929315
Miscellaneous
canSAR (ICR)LOC101929315 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929315
EVEXLOC101929315
GoPubMedLOC101929315
iHOPLOC101929315
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 : Thu Nov 9 12:05:12 CET 2017

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