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MIR614 (microRNA 614)

Identity

Alias_namesMIRN614
Alias_symbol (synonym)hsa-mir-614
Other alias
HGNC (Hugo) MIR614
LocusID (NCBI) 693199
Atlas_Id 55206
Location 12p13.1  [Link to chromosome band 12p13]
Location_base_pair Starts at 12915829 and ends at 12915918 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)

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)MIR614   32870
Cards
Entrez_Gene (NCBI)MIR614  693199  microRNA 614
AliasesMIRN614; hsa-mir-614
GeneCards (Weizmann)MIR614
Ensembl hg19 (Hinxton)ENSG00000283759 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000283759 [Gene_View]  ENSG00000283759 [Sequence]  chr12:12915829-12915918 [Contig_View]  MIR614 [Vega]
ICGC DataPortalENSG00000283759
TCGA cBioPortalMIR614
AceView (NCBI)MIR614
Genatlas (Paris)MIR614
WikiGenes693199
SOURCE (Princeton)MIR614
Genetics Home Reference (NIH)MIR614
miRBaseMIR614
dbDEMCMIR614
Genomic and cartography
GoldenPath hg38 (UCSC)MIR614  -     chr12:12915829-12915918 +  12p13.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR614  -     12p13.1   [Description]    (hg19-Feb_2009)
EnsemblMIR614 - 12p13.1 [CytoView hg19]  MIR614 - 12p13.1 [CytoView hg38]
Mapping of homologs : NCBIMIR614 [Mapview hg19]  MIR614 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR614
Alternative Splicing GalleryENSG00000283759
Gene ExpressionMIR614 [ NCBI-GEO ]   MIR614 [ EBI - ARRAY_EXPRESS ]   MIR614 [ SEEK ]   MIR614 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR614 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)693199
GTEX Portal (Tissue expression)MIR614
Human Protein AtlasENSG00000283759-MIR614 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR614
DMDM Disease mutations693199
Blocks (Seattle)MIR614
Human Protein Atlas [tissue]ENSG00000283759-MIR614 [tissue]
Protein Interaction databases
FunCoupENSG00000283759
BioGRIDMIR614
STRING (EMBL)MIR614
ZODIACMIR614
Ontologies - Pathways
Huge Navigator MIR614 [HugePedia]
snp3D : Map Gene to Disease693199
BioCentury BCIQMIR614
ClinGenMIR614
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD693199
Chemical/Pharm GKB GenePA164722910
Clinical trialMIR614
Miscellaneous
canSAR (ICR)MIR614 (select the gene name)
Probes
Litterature
PubMed5 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR614
EVEXMIR614
GoPubMedMIR614
iHOPMIR614
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Tue Nov 6 11:22:37 CET 2018

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