Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101929066 (uncharacterized LOC101929066)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929066
Atlas_Id 67483
Location 8p22  [Link to chromosome band 8p22]
Location_base_pair Starts at 18084868 and ends at 18097651 bp from pter ( according to hg38-Dec_2013)

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)LOC101929066  101929066  uncharacterized LOC101929066
Aliases
GeneCards (Weizmann)LOC101929066
Ensembl hg19 (Hinxton)ENSG00000245281 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000245281 [Gene_View]  chr8:18084868-18097651 [Contig_View]  LOC101929066 [Vega]
ICGC DataPortalENSG00000245281
TCGA cBioPortalLOC101929066
AceView (NCBI)LOC101929066
Genatlas (Paris)LOC101929066
WikiGenes101929066
SOURCE (Princeton)LOC101929066
Genetics Home Reference (NIH)LOC101929066
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929066  -     chr8:18084868-18097651 +  8p22   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929066  -     8p22   [Description]    (hg19-Feb_2009)
EnsemblLOC101929066 - 8p22 [CytoView hg19]  LOC101929066 - 8p22 [CytoView hg38]
Mapping of homologs : NCBILOC101929066 [Mapview hg19]  LOC101929066 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BX402012 CA396779 DA816173 N58047
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929066
Cluster EST : UnigeneHs.648717 [ NCBI ]
CGAP (NCI)Hs.648717
Alternative Splicing GalleryENSG00000245281
Gene ExpressionLOC101929066 [ NCBI-GEO ]   LOC101929066 [ EBI - ARRAY_EXPRESS ]   LOC101929066 [ SEEK ]   LOC101929066 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929066 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929066
GTEX Portal (Tissue expression)LOC101929066
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929066
DMDM Disease mutations101929066
Blocks (Seattle)LOC101929066
Human Protein AtlasENSG00000245281
Protein Interaction databases
FunCoupENSG00000245281
BioGRIDLOC101929066
STRING (EMBL)LOC101929066
ZODIACLOC101929066
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929066
BioCentury BCIQLOC101929066
ClinGenLOC101929066
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929066
Clinical trialLOC101929066
Miscellaneous
canSAR (ICR)LOC101929066 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929066
EVEXLOC101929066
GoPubMedLOC101929066
iHOPLOC101929066
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 : Wed Jun 7 16:06:00 CEST 2017

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