Atlas of Genetics and Cytogenetics in Oncology and Haematology


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MIR4799 (microRNA 4799)

Identity

Alias (NCBI)-
HGNC (Hugo) MIR4799
HGNC Alias symbhsa-mir-4799
LocusID (NCBI) 100616246
Atlas_Id 69713
Location 4q31.23  [Link to chromosome band 4q31]
Location_base_pair Starts at 147782595 and ends at 147782668 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)MIR4799   41584
Cards
Entrez_Gene (NCBI)MIR4799  100616246  microRNA 4799
Aliases
GeneCards (Weizmann)MIR4799
Ensembl hg19 (Hinxton)ENSG00000264274 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000264274 [Gene_View]  ENSG00000264274 [Sequence]  chr4:147782595-147782668 [Contig_View]  MIR4799 [Vega]
ICGC DataPortalENSG00000264274
TCGA cBioPortalMIR4799
AceView (NCBI)MIR4799
Genatlas (Paris)MIR4799
WikiGenes100616246
SOURCE (Princeton)MIR4799
Genetics Home Reference (NIH)MIR4799
miRBaseMIR4799
dbDEMCMIR4799
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4799  -     chr4:147782595-147782668 +  4q31.23   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4799  -     4q31.23   [Description]    (hg19-Feb_2009)
GoldenPathMIR4799 - 4q31.23 [CytoView hg19]  MIR4799 - 4q31.23 [CytoView hg38]
ImmunoBaseENSG00000264274
genome Data Viewer NCBIMIR4799 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4799
Alternative Splicing GalleryENSG00000264274
Gene ExpressionMIR4799 [ NCBI-GEO ]   MIR4799 [ EBI - ARRAY_EXPRESS ]   MIR4799 [ SEEK ]   MIR4799 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4799 [ Firebrowse - Broad ]
GenevisibleExpression of MIR4799 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100616246
GTEX Portal (Tissue expression)MIR4799
Human Protein AtlasENSG00000264274-MIR4799 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4799
DMDM Disease mutations100616246
Blocks (Seattle)MIR4799
Human Protein Atlas [tissue]ENSG00000264274-MIR4799 [tissue]
Protein Interaction databases
FunCoupENSG00000264274
BioGRIDMIR4799
STRING (EMBL)MIR4799
ZODIACMIR4799
Ontologies - Pathways
Huge Navigator MIR4799 [HugePedia]
snp3D : Map Gene to Disease100616246
BioCentury BCIQMIR4799
ClinGenMIR4799
Clinical trials, drugs, therapy
Protein Interactions : CTD100616246
Clinical trialMIR4799
Miscellaneous
canSAR (ICR)MIR4799 (select the gene name)
HarmonizomeMIR4799
DataMed IndexMIR4799
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4799
EVEXMIR4799
GoPubMedMIR4799
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 : Sat Aug 22 19:26:27 CEST 2020

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