Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumours   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

MIR522 (microRNA 522)

Identity

Alias_namesMIRN522
Alias_symbol (synonym)hsa-mir-522
Other aliasmir-522
HGNC (Hugo) MIR522
LocusID (NCBI) 574495
Atlas_Id 55614
Location 19q13.42  [Link to chromosome band 19q13]
Location_base_pair Starts at 54254465 and ends at 54254551 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)MIR522   32127
Cards
Entrez_Gene (NCBI)MIR522  574495  microRNA 522
AliasesMIRN522; hsa-mir-522; mir-522
GeneCards (Weizmann)MIR522
Ensembl hg19 (Hinxton)ENSG00000281751 [Gene_View]  chr19:54254465-54254551 [Contig_View]  MIR522 [Vega]
Ensembl hg38 (Hinxton)ENSG00000281751 [Gene_View]  chr19:54254465-54254551 [Contig_View]  MIR522 [Vega]
ICGC DataPortalENSG00000281751
TCGA cBioPortalMIR522
AceView (NCBI)MIR522
Genatlas (Paris)MIR522
WikiGenes574495
SOURCE (Princeton)MIR522
Genetics Home Reference (NIH)MIR522
miRBaseMIR522
dbDEMCMIR522
Genomic and cartography
GoldenPath hg19 (UCSC)MIR522  -     chr19:54254465-54254551 +  19q13.42   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIR522  -     19q13.42   [Description]    (hg38-Dec_2013)
EnsemblMIR522 - 19q13.42 [CytoView hg19]  MIR522 - 19q13.42 [CytoView hg38]
Mapping of homologs : NCBIMIR522 [Mapview hg19]  MIR522 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AY785936 LM609492
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000019 NC_018930 NT_011109 NW_004929415
Consensus coding sequences : CCDS (NCBI)MIR522
Alternative Splicing GalleryENSG00000281751
Gene ExpressionMIR522 [ NCBI-GEO ]   MIR522 [ EBI - ARRAY_EXPRESS ]   MIR522 [ SEEK ]   MIR522 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR522 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)574495
GTEX Portal (Tissue expression)MIR522
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR522
DMDM Disease mutations574495
Blocks (Seattle)MIR522
Human Protein AtlasENSG00000281751
Protein Interaction databases
FunCoupENSG00000281751
BioGRIDMIR522
STRING (EMBL)MIR522
ZODIACMIR522
Ontologies - Pathways
Huge Navigator MIR522 [HugePedia]
snp3D : Map Gene to Disease574495
BioCentury BCIQMIR522
ClinGenMIR522
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD574495
Chemical/Pharm GKB GenePA164722802
Clinical trialMIR522
Miscellaneous
canSAR (ICR)MIR522 (select the gene name)
Probes
Litterature
PubMed8 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR522
EVEXMIR522
GoPubMedMIR522
iHOPMIR522
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 13:16:30 CET 2017

Home   Genes   Leukemias   Solid Tumours   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.