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LOC101929709 (uncharacterized LOC101929709)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929709
Atlas_Id 76879
Location 8q21.3  [Link to chromosome band 8q21]
Location_base_pair Starts at 90729627 and ends at 90769939 bp from pter ( according to hg19-Feb_2009)
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


External links

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)LOC101929709  101929709  uncharacterized LOC101929709
Aliases
GeneCards (Weizmann)LOC101929709
Ensembl hg19 (Hinxton)ENSG00000251136 [Gene_View]  chr8:90729627-90769939 [Contig_View]  LOC101929709 [Vega]
Ensembl hg38 (Hinxton)ENSG00000251136 [Gene_View]  chr8:90729627-90769939 [Contig_View]  LOC101929709 [Vega]
ICGC DataPortalENSG00000251136
TCGA cBioPortalLOC101929709
AceView (NCBI)LOC101929709
Genatlas (Paris)LOC101929709
WikiGenes101929709
SOURCE (Princeton)LOC101929709
Genetics Home Reference (NIH)LOC101929709
Genomic and cartography
GoldenPath hg19 (UCSC)LOC101929709  -     chr8:90729627-90769939 -  8q21.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC101929709  -     8q21.3   [Description]    (hg38-Dec_2013)
EnsemblLOC101929709 - 8q21.3 [CytoView hg19]  LOC101929709 - 8q21.3 [CytoView hg38]
Mapping of homologs : NCBILOC101929709 [Mapview hg19]  LOC101929709 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BG497825 BQ007151 BQ652687 BX384738 BX538329
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000008 NC_018919 NT_008046 NW_004929340
Consensus coding sequences : CCDS (NCBI)LOC101929709
Cluster EST : UnigeneHs.729413 [ NCBI ]
CGAP (NCI)Hs.729413
Alternative Splicing GalleryENSG00000251136
Gene ExpressionLOC101929709 [ NCBI-GEO ]   LOC101929709 [ EBI - ARRAY_EXPRESS ]   LOC101929709 [ SEEK ]   LOC101929709 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929709 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929709
GTEX Portal (Tissue expression)LOC101929709
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929709
DMDM Disease mutations101929709
Blocks (Seattle)LOC101929709
Human Protein AtlasENSG00000251136
Protein Interaction databases
FunCoupENSG00000251136
BioGRIDLOC101929709
STRING (EMBL)LOC101929709
ZODIACLOC101929709
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929709
BioCentury BCIQLOC101929709
ClinGenLOC101929709
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929709
Clinical trialLOC101929709
Miscellaneous
canSAR (ICR)LOC101929709 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929709
EVEXLOC101929709
GoPubMedLOC101929709
iHOPLOC101929709
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 Mar 14 12:20:56 CET 2017

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