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MIR4790 (microRNA 4790)

Identity

Alias_symbol (synonym)hsa-mir-4790
Other alias-
HGNC (Hugo) MIR4790
LocusID (NCBI) 100616334
Atlas_Id 69704
Location 3p26.1  [Link to chromosome band 3p26]
Location_base_pair Starts at 5250177 and ends at 5250255 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)MIR4790   41820
Cards
Entrez_Gene (NCBI)MIR4790  100616334  microRNA 4790
Aliases
GeneCards (Weizmann)MIR4790
Ensembl hg19 (Hinxton)ENSG00000265180 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000265180 [Gene_View]  chr3:5250177-5250255 [Contig_View]  MIR4790 [Vega]
ICGC DataPortalENSG00000265180
TCGA cBioPortalMIR4790
AceView (NCBI)MIR4790
Genatlas (Paris)MIR4790
WikiGenes100616334
SOURCE (Princeton)MIR4790
Genetics Home Reference (NIH)MIR4790
miRBaseMIR4790
dbDEMCMIR4790
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4790  -     chr3:5250177-5250255 -  3p26.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4790  -     3p26.1   [Description]    (hg19-Feb_2009)
EnsemblMIR4790 - 3p26.1 [CytoView hg19]  MIR4790 - 3p26.1 [CytoView hg38]
Mapping of homologs : NCBIMIR4790 [Mapview hg19]  MIR4790 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4790
Alternative Splicing GalleryENSG00000265180
Gene ExpressionMIR4790 [ NCBI-GEO ]   MIR4790 [ EBI - ARRAY_EXPRESS ]   MIR4790 [ SEEK ]   MIR4790 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4790 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616334
GTEX Portal (Tissue expression)MIR4790
Human Protein AtlasENSG00000265180-MIR4790 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4790
DMDM Disease mutations100616334
Blocks (Seattle)MIR4790
Human Protein Atlas [tissue]ENSG00000265180-MIR4790 [tissue]
Protein Interaction databases
FunCoupENSG00000265180
BioGRIDMIR4790
STRING (EMBL)MIR4790
ZODIACMIR4790
Ontologies - Pathways
Huge Navigator MIR4790 [HugePedia]
snp3D : Map Gene to Disease100616334
BioCentury BCIQMIR4790
ClinGenMIR4790
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616334
Clinical trialMIR4790
Miscellaneous
canSAR (ICR)MIR4790 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4790
EVEXMIR4790
GoPubMedMIR4790
iHOPMIR4790
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 Nov 9 12:15:22 CET 2017

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