Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumors   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

MIR3152 (microRNA 3152)

Identity

Alias_symbol (synonym)hsa-mir-3152
Other alias-
HGNC (Hugo) MIR3152
LocusID (NCBI) 100422869
Atlas_Id 69171
Location 9p22.1  [Link to chromosome band 9p22]
Location_base_pair Starts at 18573306 and ends at 18573379 bp from pter ( according to hg38-Dec_2013)

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)MIR3152   38379
Cards
Entrez_Gene (NCBI)MIR3152  100422869  microRNA 3152
Aliases
GeneCards (Weizmann)MIR3152
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr9:18573306-18573379 [Contig_View]  MIR3152 [Vega]
TCGA cBioPortalMIR3152
AceView (NCBI)MIR3152
Genatlas (Paris)MIR3152
WikiGenes100422869
SOURCE (Princeton)MIR3152
Genetics Home Reference (NIH)MIR3152
miRBaseMIR3152
dbDEMCMIR3152
Genomic and cartography
GoldenPath hg38 (UCSC)MIR3152  -     chr9:18573306-18573379 +  9p22.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR3152  -     9p22.1   [Description]    (hg19-Feb_2009)
EnsemblMIR3152 - 9p22.1 [CytoView hg19]  MIR3152 - 9p22.1 [CytoView hg38]
Mapping of homologs : NCBIMIR3152 [Mapview hg19]  MIR3152 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR3152
Gene ExpressionMIR3152 [ NCBI-GEO ]   MIR3152 [ EBI - ARRAY_EXPRESS ]   MIR3152 [ SEEK ]   MIR3152 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR3152 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100422869
GTEX Portal (Tissue expression)MIR3152
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR3152
DMDM Disease mutations100422869
Blocks (Seattle)MIR3152
Protein Interaction databases
BioGRIDMIR3152
STRING (EMBL)MIR3152
ZODIACMIR3152
Ontologies - Pathways
Huge Navigator MIR3152 [HugePedia]
snp3D : Map Gene to Disease100422869
BioCentury BCIQMIR3152
ClinGenMIR3152
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100422869
Chemical/Pharm GKB GenePA165585855
Clinical trialMIR3152
Miscellaneous
canSAR (ICR)MIR3152 (select the gene name)
Probes
Litterature
PubMed5 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR3152
EVEXMIR3152
GoPubMedMIR3152
iHOPMIR3152
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 : Mon Sep 18 13:27:54 CEST 2017

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

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.