Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC100506937 (uncharacterized LOC100506937)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100506937
Atlas_Id 78152
Location 7q32.3  [Link to chromosome band 7q32]
Location_base_pair Starts at 132758970 and ends at 132760632 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)LOC100506937  100506937  uncharacterized LOC100506937
Aliases
GeneCards (Weizmann)LOC100506937
Ensembl hg19 (Hinxton)ENSG00000225881 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000225881 [Gene_View]  chr7:132758970-132760632 [Contig_View]  LOC100506937 [Vega]
ICGC DataPortalENSG00000225881
TCGA cBioPortalLOC100506937
AceView (NCBI)LOC100506937
Genatlas (Paris)LOC100506937
WikiGenes100506937
SOURCE (Princeton)LOC100506937
Genetics Home Reference (NIH)LOC100506937
Genomic and cartography
GoldenPath hg38 (UCSC)LOC100506937  -     chr7:132758970-132760632 +  7q32.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC100506937  -     7q32.3   [Description]    (hg19-Feb_2009)
EnsemblLOC100506937 - 7q32.3 [CytoView hg19]  LOC100506937 - 7q32.3 [CytoView hg38]
Mapping of homologs : NCBILOC100506937 [Mapview hg19]  LOC100506937 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BX103078
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC100506937
Cluster EST : UnigeneHs.98247 [ NCBI ]
CGAP (NCI)Hs.98247
Alternative Splicing GalleryENSG00000225881
Gene ExpressionLOC100506937 [ NCBI-GEO ]   LOC100506937 [ EBI - ARRAY_EXPRESS ]   LOC100506937 [ SEEK ]   LOC100506937 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100506937 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100506937
GTEX Portal (Tissue expression)LOC100506937
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100506937
DMDM Disease mutations100506937
Blocks (Seattle)LOC100506937
Human Protein AtlasENSG00000225881
Protein Interaction databases
FunCoupENSG00000225881
BioGRIDLOC100506937
STRING (EMBL)LOC100506937
ZODIACLOC100506937
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100506937
BioCentury BCIQLOC100506937
ClinGenLOC100506937
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100506937
Clinical trialLOC100506937
Miscellaneous
canSAR (ICR)LOC100506937 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100506937
EVEXLOC100506937
GoPubMedLOC100506937
iHOPLOC100506937
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 16:02:51 CEST 2017

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