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LOC100506928 (uncharacterized LOC100506928)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100506928
Atlas_Id 66858
Location 16p11.2  [Link to chromosome band 16p11]
Location_base_pair Starts at 30041594 and ends at 30499554 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)LOC100506928  100506928  uncharacterized LOC100506928
Aliases
GeneCards (Weizmann)LOC100506928
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr16:30041594-30499554 [Contig_View]  LOC100506928 [Vega]
TCGA cBioPortalLOC100506928
AceView (NCBI)LOC100506928
Genatlas (Paris)LOC100506928
WikiGenes100506928
SOURCE (Princeton)LOC100506928
Genetics Home Reference (NIH)LOC100506928
Genomic and cartography
GoldenPath hg38 (UCSC)LOC100506928  -     chr16:30041594-30499554 -  16p11.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC100506928  -     16p11.2   [Description]    (hg19-Feb_2009)
EnsemblLOC100506928 - 16p11.2 [CytoView hg19]  LOC100506928 - 16p11.2 [CytoView hg38]
Mapping of homologs : NCBILOC100506928 [Mapview hg19]  LOC100506928 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK123224
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC100506928
Cluster EST : UnigeneHs.587874 [ NCBI ]
CGAP (NCI)Hs.587874
Gene ExpressionLOC100506928 [ NCBI-GEO ]   LOC100506928 [ EBI - ARRAY_EXPRESS ]   LOC100506928 [ SEEK ]   LOC100506928 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100506928 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100506928
GTEX Portal (Tissue expression)LOC100506928
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100506928
DMDM Disease mutations100506928
Blocks (Seattle)LOC100506928
IPIIPI00446727   
Protein Interaction databases
BioGRIDLOC100506928
STRING (EMBL)LOC100506928
ZODIACLOC100506928
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100506928
BioCentury BCIQLOC100506928
ClinGenLOC100506928
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100506928
Clinical trialLOC100506928
Miscellaneous
canSAR (ICR)LOC100506928 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100506928
EVEXLOC100506928
GoPubMedLOC100506928
iHOPLOC100506928
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 : Thu Nov 9 12:02:06 CET 2017

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