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

MIR769 (microRNA 769)

Identity

Alias_namesMIRN769
Alias_symbol (synonym)hsa-mir-769
Other aliasmir-769
HGNC (Hugo) MIR769
LocusID (NCBI) 768217
Atlas_Id 70232
Location 19q13.32  [Link to chromosome band 19q13]
Location_base_pair Starts at 46522190 and ends at 46522307 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)MIR769   33138
Cards
Entrez_Gene (NCBI)MIR769  768217  microRNA 769
AliasesMIRN769; hsa-mir-769; mir-769
GeneCards (Weizmann)MIR769
Ensembl hg19 (Hinxton)ENSG00000211580 [Gene_View]  chr19:46522190-46522307 [Contig_View]  MIR769 [Vega]
Ensembl hg38 (Hinxton)ENSG00000211580 [Gene_View]  chr19:46522190-46522307 [Contig_View]  MIR769 [Vega]
ICGC DataPortalENSG00000211580
TCGA cBioPortalMIR769
AceView (NCBI)MIR769
Genatlas (Paris)MIR769
WikiGenes768217
SOURCE (Princeton)MIR769
Genetics Home Reference (NIH)MIR769
miRBaseMIR769
dbDEMCMIR769
Genomic and cartography
GoldenPath hg19 (UCSC)MIR769  -     chr19:46522190-46522307 +  19q13.32   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIR769  -     19q13.32   [Description]    (hg38-Dec_2013)
EnsemblMIR769 - 19q13.32 [CytoView hg19]  MIR769 - 19q13.32 [CytoView hg38]
Mapping of homologs : NCBIMIR769 [Mapview hg19]  MIR769 [Mapview hg38]
Gene and transcription
Genbank (Entrez)LM609635
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000019 NC_018930 NT_011109 NW_004929415
Consensus coding sequences : CCDS (NCBI)MIR769
Alternative Splicing GalleryENSG00000211580
Gene ExpressionMIR769 [ NCBI-GEO ]   MIR769 [ EBI - ARRAY_EXPRESS ]   MIR769 [ SEEK ]   MIR769 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR769 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)768217
GTEX Portal (Tissue expression)MIR769
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR769
DMDM Disease mutations768217
Blocks (Seattle)MIR769
Human Protein AtlasENSG00000211580
Protein Interaction databases
FunCoupENSG00000211580
BioGRIDMIR769
STRING (EMBL)MIR769
ZODIACMIR769
Ontologies - Pathways
Huge Navigator MIR769 [HugePedia]
snp3D : Map Gene to Disease768217
BioCentury BCIQMIR769
ClinGenMIR769
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD768217
Chemical/Pharm GKB GenePA164722977
Clinical trialMIR769
Miscellaneous
canSAR (ICR)MIR769 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR769
EVEXMIR769
GoPubMedMIR769
iHOPMIR769
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 12:32:56 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.