Atlas of Genetics and Cytogenetics in Oncology and Haematology


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MIR4419B (microRNA 4419b)

Identity

Alias_symbol (synonym)hsa-mir-4419b
Other alias-
HGNC (Hugo) MIR4419B
LocusID (NCBI) 100616298
Atlas_Id 76884
Location 12q24.32  [Link to chromosome band 12q24]
Location_base_pair Starts at 128244506 and ends at 128244573 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)MIR4419B   41724
Cards
Entrez_Gene (NCBI)MIR4419B  100616298  microRNA 4419b
Aliases
GeneCards (Weizmann)MIR4419B
Ensembl hg19 (Hinxton)ENSG00000265061 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000265061 [Gene_View]  chr12:128244506-128244573 [Contig_View]  MIR4419B [Vega]
ICGC DataPortalENSG00000265061
TCGA cBioPortalMIR4419B
AceView (NCBI)MIR4419B
Genatlas (Paris)MIR4419B
WikiGenes100616298
SOURCE (Princeton)MIR4419B
Genetics Home Reference (NIH)MIR4419B
miRBaseMIR4419B
dbDEMCMIR4419B
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4419B  -     chr12:128244506-128244573 +  12q24.32   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4419B  -     12q24.32   [Description]    (hg19-Feb_2009)
EnsemblMIR4419B - 12q24.32 [CytoView hg19]  MIR4419B - 12q24.32 [CytoView hg38]
Mapping of homologs : NCBIMIR4419B [Mapview hg19]  MIR4419B [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4419B
Alternative Splicing GalleryENSG00000265061
Gene ExpressionMIR4419B [ NCBI-GEO ]   MIR4419B [ EBI - ARRAY_EXPRESS ]   MIR4419B [ SEEK ]   MIR4419B [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4419B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616298
GTEX Portal (Tissue expression)MIR4419B
Human Protein AtlasENSG00000265061-MIR4419B [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4419B
DMDM Disease mutations100616298
Blocks (Seattle)MIR4419B
Human Protein Atlas [tissue]ENSG00000265061-MIR4419B [tissue]
Protein Interaction databases
FunCoupENSG00000265061
BioGRIDMIR4419B
STRING (EMBL)MIR4419B
ZODIACMIR4419B
Ontologies - Pathways
Huge Navigator MIR4419B [HugePedia]
snp3D : Map Gene to Disease100616298
BioCentury BCIQMIR4419B
ClinGenMIR4419B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616298
Clinical trialMIR4419B
Miscellaneous
canSAR (ICR)MIR4419B (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4419B
EVEXMIR4419B
GoPubMedMIR4419B
iHOPMIR4419B
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Thu Nov 9 12:14:23 CET 2017

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