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MIR4798 (microRNA 4798)

Identity

Alias (NCBI)-
HGNC (Hugo) MIR4798
HGNC Alias symbhsa-mir-4798
LocusID (NCBI) 100616471
Atlas_Id 69712
Location 4p16.1  [Link to chromosome band 4p16]
Location_base_pair Starts at 7310450 and ends at 7310524 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)MIR4798   41616
Cards
Entrez_Gene (NCBI)MIR4798  100616471  microRNA 4798
Aliases
GeneCards (Weizmann)MIR4798
Ensembl hg19 (Hinxton)ENSG00000264658 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000264658 [Gene_View]  ENSG00000264658 [Sequence]  chr4:7310450-7310524 [Contig_View]  MIR4798 [Vega]
ICGC DataPortalENSG00000264658
TCGA cBioPortalMIR4798
AceView (NCBI)MIR4798
Genatlas (Paris)MIR4798
WikiGenes100616471
SOURCE (Princeton)MIR4798
Genetics Home Reference (NIH)MIR4798
miRBaseMIR4798
dbDEMCMIR4798
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4798  -     chr4:7310450-7310524 +  4p16.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4798  -     4p16.1   [Description]    (hg19-Feb_2009)
GoldenPathMIR4798 - 4p16.1 [CytoView hg19]  MIR4798 - 4p16.1 [CytoView hg38]
ImmunoBaseENSG00000264658
genome Data Viewer NCBIMIR4798 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4798
Alternative Splicing GalleryENSG00000264658
Gene ExpressionMIR4798 [ NCBI-GEO ]   MIR4798 [ EBI - ARRAY_EXPRESS ]   MIR4798 [ SEEK ]   MIR4798 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4798 [ Firebrowse - Broad ]
GenevisibleExpression of MIR4798 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100616471
GTEX Portal (Tissue expression)MIR4798
Human Protein AtlasENSG00000264658-MIR4798 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4798
DMDM Disease mutations100616471
Blocks (Seattle)MIR4798
Human Protein Atlas [tissue]ENSG00000264658-MIR4798 [tissue]
Protein Interaction databases
FunCoupENSG00000264658
BioGRIDMIR4798
STRING (EMBL)MIR4798
ZODIACMIR4798
Ontologies - Pathways
Huge Navigator MIR4798 [HugePedia]
snp3D : Map Gene to Disease100616471
BioCentury BCIQMIR4798
ClinGenMIR4798
Clinical trials, drugs, therapy
Protein Interactions : CTD100616471
Clinical trialMIR4798
Miscellaneous
canSAR (ICR)MIR4798 (select the gene name)
HarmonizomeMIR4798
DataMed IndexMIR4798
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4798
EVEXMIR4798
GoPubMedMIR4798
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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