Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC100505716 (uncharacterized LOC100505716)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100505716
Atlas_Id 66749
Location 2p23.2  [Link to chromosome band 2p23]
Location_base_pair Starts at 28530558 and ends at 28533326 bp from pter ( according to hg19-Feb_2009)

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)LOC100505716  100505716  uncharacterized LOC100505716
Aliases
GeneCards (Weizmann)LOC100505716
Ensembl hg19 (Hinxton)ENSG00000223522 [Gene_View]  chr2:28530558-28533326 [Contig_View]  LOC100505716 [Vega]
Ensembl hg38 (Hinxton)ENSG00000223522 [Gene_View]  chr2:28530558-28533326 [Contig_View]  LOC100505716 [Vega]
ICGC DataPortalENSG00000223522
TCGA cBioPortalLOC100505716
AceView (NCBI)LOC100505716
Genatlas (Paris)LOC100505716
WikiGenes100505716
SOURCE (Princeton)LOC100505716
Genetics Home Reference (NIH)LOC100505716
Genomic and cartography
GoldenPath hg19 (UCSC)LOC100505716  -     chr2:28530558-28533326 -  2p23.2   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC100505716  -     2p23.2   [Description]    (hg38-Dec_2013)
EnsemblLOC100505716 - 2p23.2 [CytoView hg19]  LOC100505716 - 2p23.2 [CytoView hg38]
Mapping of homologs : NCBILOC100505716 [Mapview hg19]  LOC100505716 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC041993 HG493790
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000002 NC_018913 NT_022184 NW_004929300
Consensus coding sequences : CCDS (NCBI)LOC100505716
Cluster EST : UnigeneHs.679092 [ NCBI ]
CGAP (NCI)Hs.679092
Alternative Splicing GalleryENSG00000223522
Gene ExpressionLOC100505716 [ NCBI-GEO ]   LOC100505716 [ EBI - ARRAY_EXPRESS ]   LOC100505716 [ SEEK ]   LOC100505716 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100505716 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100505716
GTEX Portal (Tissue expression)LOC100505716
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100505716
DMDM Disease mutations100505716
Blocks (Seattle)LOC100505716
Human Protein AtlasENSG00000223522
Protein Interaction databases
FunCoupENSG00000223522
BioGRIDLOC100505716
STRING (EMBL)LOC100505716
ZODIACLOC100505716
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100505716
BioCentury BCIQLOC100505716
ClinGenLOC100505716
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100505716
Clinical trialLOC100505716
Miscellaneous
canSAR (ICR)LOC100505716 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100505716
EVEXLOC100505716
GoPubMedLOC100505716
iHOPLOC100505716
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 Mar 14 12:16:52 CET 2017

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