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

MIR3187 (microRNA 3187)

Identity

Alias_symbol (synonym)hsa-mir-3187
Other aliasmir-3187
HGNC (Hugo) MIR3187
LocusID (NCBI) 100422854
Atlas_Id 69207
Location 19p13.3  [Link to chromosome band 19p13]
Location_base_pair Starts at 813584 and ends at 813653 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)MIR3187   38319
Cards
Entrez_Gene (NCBI)MIR3187  100422854  microRNA 3187
Aliasesmir-3187
GeneCards (Weizmann)MIR3187
Ensembl hg19 (Hinxton)ENSG00000263414 [Gene_View]  chr19:813584-813653 [Contig_View]  MIR3187 [Vega]
Ensembl hg38 (Hinxton)ENSG00000263414 [Gene_View]  chr19:813584-813653 [Contig_View]  MIR3187 [Vega]
ICGC DataPortalENSG00000263414
TCGA cBioPortalMIR3187
AceView (NCBI)MIR3187
Genatlas (Paris)MIR3187
WikiGenes100422854
SOURCE (Princeton)MIR3187
Genetics Home Reference (NIH)MIR3187
miRBaseMIR3187
dbDEMCMIR3187
Genomic and cartography
GoldenPath hg19 (UCSC)MIR3187  -     chr19:813584-813653 +  19p13.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIR3187  -     19p13.3   [Description]    (hg38-Dec_2013)
EnsemblMIR3187 - 19p13.3 [CytoView hg19]  MIR3187 - 19p13.3 [CytoView hg38]
Mapping of homologs : NCBIMIR3187 [Mapview hg19]  MIR3187 [Mapview hg38]
Gene and transcription
Genbank (Entrez)LM611044
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000019 NC_018930 NT_011295 NW_004929412
Consensus coding sequences : CCDS (NCBI)MIR3187
Alternative Splicing GalleryENSG00000263414
Gene ExpressionMIR3187 [ NCBI-GEO ]   MIR3187 [ EBI - ARRAY_EXPRESS ]   MIR3187 [ SEEK ]   MIR3187 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR3187 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100422854
GTEX Portal (Tissue expression)MIR3187
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR3187
DMDM Disease mutations100422854
Blocks (Seattle)MIR3187
Human Protein AtlasENSG00000263414
Protein Interaction databases
FunCoupENSG00000263414
BioGRIDMIR3187
STRING (EMBL)MIR3187
ZODIACMIR3187
Ontologies - Pathways
Huge Navigator MIR3187 [HugePedia]
snp3D : Map Gene to Disease100422854
BioCentury BCIQMIR3187
ClinGenMIR3187
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100422854
Chemical/Pharm GKB GenePA165393756
Clinical trialMIR3187
Miscellaneous
canSAR (ICR)MIR3187 (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR3187
EVEXMIR3187
GoPubMedMIR3187
iHOPMIR3187
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 12:29:11 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.