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LOC100506368 (uncharacterized LOC100506368)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100506368
Atlas_Id 66807
Location 11q14.2  [Link to chromosome band 11q14]
Location_base_pair Starts at 86955621 and ends at 87000947 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)LOC100506368  100506368  uncharacterized LOC100506368
Aliases
GeneCards (Weizmann)LOC100506368
Ensembl hg19 (Hinxton)ENSG00000246523 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000246523 [Gene_View]  chr11:86955621-87000947 [Contig_View]  LOC100506368 [Vega]
ICGC DataPortalENSG00000246523
TCGA cBioPortalLOC100506368
AceView (NCBI)LOC100506368
Genatlas (Paris)LOC100506368
WikiGenes100506368
SOURCE (Princeton)LOC100506368
Genetics Home Reference (NIH)LOC100506368
Genomic and cartography
GoldenPath hg38 (UCSC)LOC100506368  -     chr11:86955621-87000947 +  11q14.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC100506368  -     11q14.2   [Description]    (hg19-Feb_2009)
EnsemblLOC100506368 - 11q14.2 [CytoView hg19]  LOC100506368 - 11q14.2 [CytoView hg38]
Mapping of homologs : NCBILOC100506368 [Mapview hg19]  LOC100506368 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC041984
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC100506368
Cluster EST : UnigeneHs.559920 [ NCBI ]
CGAP (NCI)Hs.559920
Alternative Splicing GalleryENSG00000246523
Gene ExpressionLOC100506368 [ NCBI-GEO ]   LOC100506368 [ EBI - ARRAY_EXPRESS ]   LOC100506368 [ SEEK ]   LOC100506368 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100506368 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100506368
GTEX Portal (Tissue expression)LOC100506368
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100506368
DMDM Disease mutations100506368
Blocks (Seattle)LOC100506368
Human Protein AtlasENSG00000246523
Protein Interaction databases
FunCoupENSG00000246523
BioGRIDLOC100506368
STRING (EMBL)LOC100506368
ZODIACLOC100506368
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100506368
BioCentury BCIQLOC100506368
ClinGenLOC100506368
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100506368
Clinical trialLOC100506368
Miscellaneous
canSAR (ICR)LOC100506368 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100506368
EVEXLOC100506368
GoPubMedLOC100506368
iHOPLOC100506368
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 16:02:38 CEST 2017

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