Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC100506282 (uncharacterized LOC100506282)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100506282
Atlas_Id 66802
Location 11q14.1  [Link to chromosome band 11q14]
Location_base_pair Starts at 83192137 and ends at 83193639 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)
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)LOC100506282  100506282  uncharacterized LOC100506282
Aliases
GeneCards (Weizmann)LOC100506282
Ensembl hg19 (Hinxton)ENSG00000247137 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000247137 [Gene_View]  chr11:83192137-83193639 [Contig_View]  LOC100506282 [Vega]
ICGC DataPortalENSG00000247137
TCGA cBioPortalLOC100506282
AceView (NCBI)LOC100506282
Genatlas (Paris)LOC100506282
WikiGenes100506282
SOURCE (Princeton)LOC100506282
Genetics Home Reference (NIH)LOC100506282
Genomic and cartography
GoldenPath hg38 (UCSC)LOC100506282  -     chr11:83192137-83193639 -  11q14.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC100506282  -     11q14.1   [Description]    (hg19-Feb_2009)
EnsemblLOC100506282 - 11q14.1 [CytoView hg19]  LOC100506282 - 11q14.1 [CytoView hg38]
Mapping of homologs : NCBILOC100506282 [Mapview hg19]  LOC100506282 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK311356 AL359570
RefSeq transcript (Entrez)NM_018705
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC100506282
Cluster EST : UnigeneHs.585502 [ NCBI ]
CGAP (NCI)Hs.585502
Alternative Splicing GalleryENSG00000247137
Gene ExpressionLOC100506282 [ NCBI-GEO ]   LOC100506282 [ EBI - ARRAY_EXPRESS ]   LOC100506282 [ SEEK ]   LOC100506282 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100506282 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100506282
GTEX Portal (Tissue expression)LOC100506282
Human Protein AtlasENSG00000247137-LOC100506282 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100506282
DMDM Disease mutations100506282
Blocks (Seattle)LOC100506282
Human Protein Atlas [tissue]ENSG00000247137-LOC100506282 [tissue]
Protein Interaction databases
FunCoupENSG00000247137
BioGRIDLOC100506282
STRING (EMBL)LOC100506282
ZODIACLOC100506282
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100506282
BioCentury BCIQLOC100506282
ClinGenLOC100506282
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100506282
Clinical trialLOC100506282
Miscellaneous
canSAR (ICR)LOC100506282 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100506282
EVEXLOC100506282
GoPubMedLOC100506282
iHOPLOC100506282
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 Nov 21 13:48:39 CET 2017

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