Atlas of Genetics and Cytogenetics in Oncology and Haematology


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MIR1469 (microRNA 1469)

Identity

Alias (NCBI)MIRN1469
hsa-mir-1469
HGNC (Hugo) MIR1469
HGNC Alias symbhsa-mir-1469
HGNC Previous nameMIRN1469
LocusID (NCBI) 100302258
Atlas_Id 69081
Location 15q26.2  [Link to chromosome band 15q26]
Location_base_pair Starts at 96333261 and ends at 96333307 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)MIR1469   35378
Cards
Entrez_Gene (NCBI)MIR1469  100302258  microRNA 1469
AliasesMIRN1469; hsa-mir-1469
GeneCards (Weizmann)MIR1469
Ensembl hg19 (Hinxton)ENSG00000283888 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000283888 [Gene_View]  ENSG00000283888 [Sequence]  chr15:96333261-96333307 [Contig_View]  MIR1469 [Vega]
ICGC DataPortalENSG00000283888
TCGA cBioPortalMIR1469
AceView (NCBI)MIR1469
Genatlas (Paris)MIR1469
WikiGenes100302258
SOURCE (Princeton)MIR1469
Genetics Home Reference (NIH)MIR1469
miRBaseMIR1469
dbDEMCMIR1469
Genomic and cartography
GoldenPath hg38 (UCSC)MIR1469  -     chr15:96333261-96333307 +  15q26.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR1469  -     15q26.2   [Description]    (hg19-Feb_2009)
GoldenPathMIR1469 - 15q26.2 [CytoView hg19]  MIR1469 - 15q26.2 [CytoView hg38]
ImmunoBaseENSG00000283888
genome Data Viewer NCBIMIR1469 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR1469
Alternative Splicing GalleryENSG00000283888
Gene ExpressionMIR1469 [ NCBI-GEO ]   MIR1469 [ EBI - ARRAY_EXPRESS ]   MIR1469 [ SEEK ]   MIR1469 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR1469 [ Firebrowse - Broad ]
GenevisibleExpression of MIR1469 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100302258
GTEX Portal (Tissue expression)MIR1469
Human Protein AtlasENSG00000283888-MIR1469 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR1469
DMDM Disease mutations100302258
Blocks (Seattle)MIR1469
Human Protein Atlas [tissue]ENSG00000283888-MIR1469 [tissue]
Protein Interaction databases
FunCoupENSG00000283888
BioGRIDMIR1469
STRING (EMBL)MIR1469
ZODIACMIR1469
Ontologies - Pathways
Huge Navigator MIR1469 [HugePedia]
snp3D : Map Gene to Disease100302258
BioCentury BCIQMIR1469
ClinGenMIR1469
Clinical trials, drugs, therapy
Protein Interactions : CTD100302258
Pharm GKB GenePA164722496
Clinical trialMIR1469
Miscellaneous
canSAR (ICR)MIR1469 (select the gene name)
HarmonizomeMIR1469
DataMed IndexMIR1469
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR1469
EVEXMIR1469
GoPubMedMIR1469
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Thu Jul 16 16:14:04 CEST 2020

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