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MIR4462 (microRNA 4462)

Identity

Alias_symbol (synonym)hsa-mir-4462
Other alias-
HGNC (Hugo) MIR4462
LocusID (NCBI) 100616413
Atlas_Id 69474
Location 6p21.2  [Link to chromosome band 6p21]
Location_base_pair Starts at 37555366 and ends at 37555422 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)MIR4462   41549
Cards
Entrez_Gene (NCBI)MIR4462  100616413  microRNA 4462
Aliases
GeneCards (Weizmann)MIR4462
Ensembl hg19 (Hinxton)ENSG00000263926 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000263926 [Gene_View]  ENSG00000263926 [Sequence]  chr6:37555366-37555422 [Contig_View]  MIR4462 [Vega]
ICGC DataPortalENSG00000263926
TCGA cBioPortalMIR4462
AceView (NCBI)MIR4462
Genatlas (Paris)MIR4462
WikiGenes100616413
SOURCE (Princeton)MIR4462
Genetics Home Reference (NIH)MIR4462
miRBaseMIR4462
dbDEMCMIR4462
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4462  -     chr6:37555366-37555422 -  6p21.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4462  -     6p21.2   [Description]    (hg19-Feb_2009)
EnsemblMIR4462 - 6p21.2 [CytoView hg19]  MIR4462 - 6p21.2 [CytoView hg38]
Mapping of homologs : NCBIMIR4462 [Mapview hg19]  MIR4462 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4462
Alternative Splicing GalleryENSG00000263926
Gene ExpressionMIR4462 [ NCBI-GEO ]   MIR4462 [ EBI - ARRAY_EXPRESS ]   MIR4462 [ SEEK ]   MIR4462 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4462 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616413
GTEX Portal (Tissue expression)MIR4462
Human Protein AtlasENSG00000263926-MIR4462 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4462
DMDM Disease mutations100616413
Blocks (Seattle)MIR4462
Human Protein Atlas [tissue]ENSG00000263926-MIR4462 [tissue]
Protein Interaction databases
FunCoupENSG00000263926
BioGRIDMIR4462
STRING (EMBL)MIR4462
ZODIACMIR4462
Ontologies - Pathways
Huge Navigator MIR4462 [HugePedia]
snp3D : Map Gene to Disease100616413
BioCentury BCIQMIR4462
ClinGenMIR4462
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616413
Clinical trialMIR4462
Miscellaneous
canSAR (ICR)MIR4462 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4462
EVEXMIR4462
GoPubMedMIR4462
iHOPMIR4462
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 : Mon Jul 30 14:14:46 CEST 2018

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