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LOC100506289 (uncharacterized LOC100506289)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100506289
Atlas_Id 77292
Location 7p15.2  [Link to chromosome band 7p15]
Location_base_pair Starts at 26551822 and ends at 26557200 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


External links

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)LOC100506289  100506289  uncharacterized LOC100506289
Aliases
GeneCards (Weizmann)LOC100506289
Ensembl hg19 (Hinxton)ENSG00000233760 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000233760 [Gene_View]  chr7:26551822-26557200 [Contig_View]  LOC100506289 [Vega]
ICGC DataPortalENSG00000233760
TCGA cBioPortalLOC100506289
AceView (NCBI)LOC100506289
Genatlas (Paris)LOC100506289
WikiGenes100506289
SOURCE (Princeton)LOC100506289
Genetics Home Reference (NIH)LOC100506289
Genomic and cartography
GoldenPath hg38 (UCSC)LOC100506289  -     chr7:26551822-26557200 +  7p15.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC100506289  -     7p15.2   [Description]    (hg19-Feb_2009)
EnsemblLOC100506289 - 7p15.2 [CytoView hg19]  LOC100506289 - 7p15.2 [CytoView hg38]
Mapping of homologs : NCBILOC100506289 [Mapview hg19]  LOC100506289 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BX537871
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC100506289
Cluster EST : UnigeneHs.114761 [ NCBI ]
CGAP (NCI)Hs.114761
Alternative Splicing GalleryENSG00000233760
Gene ExpressionLOC100506289 [ NCBI-GEO ]   LOC100506289 [ EBI - ARRAY_EXPRESS ]   LOC100506289 [ SEEK ]   LOC100506289 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100506289 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100506289
GTEX Portal (Tissue expression)LOC100506289
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100506289
DMDM Disease mutations100506289
Blocks (Seattle)LOC100506289
Human Protein AtlasENSG00000233760
Protein Interaction databases
FunCoupENSG00000233760
BioGRIDLOC100506289
STRING (EMBL)LOC100506289
ZODIACLOC100506289
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100506289
BioCentury BCIQLOC100506289
ClinGenLOC100506289
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100506289
Clinical trialLOC100506289
Miscellaneous
canSAR (ICR)LOC100506289 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100506289
EVEXLOC100506289
GoPubMedLOC100506289
iHOPLOC100506289
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 16:02:36 CEST 2017

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