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MIR4465 (microRNA 4465)

Identity

Alias_symbol (synonym)hsa-mir-4465
Other alias-
HGNC (Hugo) MIR4465
LocusID (NCBI) 100616180
Atlas_Id 69476
Location 6q24.1  [Link to chromosome band 6q24]
Location_base_pair Starts at 140683814 and ends at 140683883 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)MIR4465   41842
Cards
Entrez_Gene (NCBI)MIR4465  100616180  microRNA 4465
Aliases
GeneCards (Weizmann)MIR4465
Ensembl hg19 (Hinxton)ENSG00000264390 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000264390 [Gene_View]  ENSG00000264390 [Sequence]  chr6:140683814-140683883 [Contig_View]  MIR4465 [Vega]
ICGC DataPortalENSG00000264390
TCGA cBioPortalMIR4465
AceView (NCBI)MIR4465
Genatlas (Paris)MIR4465
WikiGenes100616180
SOURCE (Princeton)MIR4465
Genetics Home Reference (NIH)MIR4465
miRBaseMIR4465
dbDEMCMIR4465
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4465  -     chr6:140683814-140683883 +  6q24.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4465  -     6q24.1   [Description]    (hg19-Feb_2009)
EnsemblMIR4465 - 6q24.1 [CytoView hg19]  MIR4465 - 6q24.1 [CytoView hg38]
Mapping of homologs : NCBIMIR4465 [Mapview hg19]  MIR4465 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4465
Alternative Splicing GalleryENSG00000264390
Gene ExpressionMIR4465 [ NCBI-GEO ]   MIR4465 [ EBI - ARRAY_EXPRESS ]   MIR4465 [ SEEK ]   MIR4465 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4465 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616180
GTEX Portal (Tissue expression)MIR4465
Human Protein AtlasENSG00000264390-MIR4465 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4465
DMDM Disease mutations100616180
Blocks (Seattle)MIR4465
Human Protein Atlas [tissue]ENSG00000264390-MIR4465 [tissue]
Protein Interaction databases
FunCoupENSG00000264390
BioGRIDMIR4465
STRING (EMBL)MIR4465
ZODIACMIR4465
Ontologies - Pathways
Huge Navigator MIR4465 [HugePedia]
snp3D : Map Gene to Disease100616180
BioCentury BCIQMIR4465
ClinGenMIR4465
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616180
Clinical trialMIR4465
Miscellaneous
canSAR (ICR)MIR4465 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4465
EVEXMIR4465
GoPubMedMIR4465
iHOPMIR4465
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 : Mon Jul 30 14:14:46 CEST 2018

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