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MIR3665 (microRNA 3665)

Identity

Alias_symbol (synonym)hsa-mir-3665
Other alias-
HGNC (Hugo) MIR3665
LocusID (NCBI) 100500861
Atlas_Id 69274
Location 13q22.3  [Link to chromosome band 13q22]
Location_base_pair Starts at 78272147 and ends at 78272251 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)MIR3665   38939
Cards
Entrez_Gene (NCBI)MIR3665  100500861  microRNA 3665
Aliases
GeneCards (Weizmann)MIR3665
Ensembl hg19 (Hinxton)ENSG00000266325 [Gene_View]  chr13:78272147-78272251 [Contig_View]  MIR3665 [Vega]
Ensembl hg38 (Hinxton)ENSG00000266325 [Gene_View]  chr13:78272147-78272251 [Contig_View]  MIR3665 [Vega]
ICGC DataPortalENSG00000266325
TCGA cBioPortalMIR3665
AceView (NCBI)MIR3665
Genatlas (Paris)MIR3665
WikiGenes100500861
SOURCE (Princeton)MIR3665
Genetics Home Reference (NIH)MIR3665
miRBaseMIR3665
dbDEMCMIR3665
Genomic and cartography
GoldenPath hg19 (UCSC)MIR3665  -     chr13:78272147-78272251 -  13q22.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIR3665  -     13q22.3   [Description]    (hg38-Dec_2013)
EnsemblMIR3665 - 13q22.3 [CytoView hg19]  MIR3665 - 13q22.3 [CytoView hg38]
Mapping of homologs : NCBIMIR3665 [Mapview hg19]  MIR3665 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000013 NC_018924 NT_024524 NW_004929388
Consensus coding sequences : CCDS (NCBI)MIR3665
Alternative Splicing GalleryENSG00000266325
Gene ExpressionMIR3665 [ NCBI-GEO ]   MIR3665 [ EBI - ARRAY_EXPRESS ]   MIR3665 [ SEEK ]   MIR3665 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR3665 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100500861
GTEX Portal (Tissue expression)MIR3665
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR3665
DMDM Disease mutations100500861
Blocks (Seattle)MIR3665
Human Protein AtlasENSG00000266325
Protein Interaction databases
FunCoupENSG00000266325
BioGRIDMIR3665
STRING (EMBL)MIR3665
ZODIACMIR3665
Ontologies - Pathways
Huge Navigator MIR3665 [HugePedia]
snp3D : Map Gene to Disease100500861
BioCentury BCIQMIR3665
ClinGenMIR3665
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100500861
Clinical trialMIR3665
Miscellaneous
canSAR (ICR)MIR3665 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR3665
EVEXMIR3665
GoPubMedMIR3665
iHOPMIR3665
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

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indexed on : Tue Mar 14 12:29:23 CET 2017

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