Atlas of Genetics and Cytogenetics in Oncology and Haematology


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MIR4715 (microRNA 4715)

Identity

Alias (NCBI)-
HGNC (Hugo) MIR4715
HGNC Alias symbhsa-mir-4715
LocusID (NCBI) 100616474
Atlas_Id 69629
Location 15q12  [Link to chromosome band 15q12]
Location_base_pair Starts at 25848747 and ends at 25848825 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)MIR4715   41666
Cards
Entrez_Gene (NCBI)MIR4715  100616474  microRNA 4715
Aliases
GeneCards (Weizmann)MIR4715
Ensembl hg19 (Hinxton)ENSG00000266517 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000266517 [Gene_View]  ENSG00000266517 [Sequence]  chr15:25848747-25848825 [Contig_View]  MIR4715 [Vega]
ICGC DataPortalENSG00000266517
TCGA cBioPortalMIR4715
AceView (NCBI)MIR4715
Genatlas (Paris)MIR4715
WikiGenes100616474
SOURCE (Princeton)MIR4715
Genetics Home Reference (NIH)MIR4715
miRBaseMIR4715
dbDEMCMIR4715
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4715  -     chr15:25848747-25848825 -  15q12   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4715  -     15q12   [Description]    (hg19-Feb_2009)
GoldenPathMIR4715 - 15q12 [CytoView hg19]  MIR4715 - 15q12 [CytoView hg38]
ImmunoBaseENSG00000266517
genome Data Viewer NCBIMIR4715 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4715
Alternative Splicing GalleryENSG00000266517
Gene ExpressionMIR4715 [ NCBI-GEO ]   MIR4715 [ EBI - ARRAY_EXPRESS ]   MIR4715 [ SEEK ]   MIR4715 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4715 [ Firebrowse - Broad ]
GenevisibleExpression of MIR4715 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100616474
GTEX Portal (Tissue expression)MIR4715
Human Protein AtlasENSG00000266517-MIR4715 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4715
DMDM Disease mutations100616474
Blocks (Seattle)MIR4715
Human Protein Atlas [tissue]ENSG00000266517-MIR4715 [tissue]
Protein Interaction databases
FunCoupENSG00000266517
BioGRIDMIR4715
STRING (EMBL)MIR4715
ZODIACMIR4715
Ontologies - Pathways
Huge Navigator MIR4715 [HugePedia]
snp3D : Map Gene to Disease100616474
BioCentury BCIQMIR4715
ClinGenMIR4715
Clinical trials, drugs, therapy
Protein Interactions : CTD100616474
Clinical trialMIR4715
Miscellaneous
canSAR (ICR)MIR4715 (select the gene name)
HarmonizomeMIR4715
DataMed IndexMIR4715
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4715
EVEXMIR4715
GoPubMedMIR4715
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 : Thu Jul 16 16:15:57 CEST 2020

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