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MIR4490 (microRNA 4490)

Identity

Alias_symbol (synonym)hsa-mir-4490
Other alias-
HGNC (Hugo) MIR4490
LocusID (NCBI) 100616186
Atlas_Id 69499
Location 11q14.3  [Link to chromosome band 11q14]
Location_base_pair Starts at 90288942 and ends at 90289025 bp from pter ( according to hg19-Feb_2009)

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)MIR4490   41871
Cards
Entrez_Gene (NCBI)MIR4490  100616186  microRNA 4490
Aliases
GeneCards (Weizmann)MIR4490
Ensembl hg19 (Hinxton)ENSG00000266703 [Gene_View]  chr11:90288942-90289025 [Contig_View]  MIR4490 [Vega]
Ensembl hg38 (Hinxton)ENSG00000266703 [Gene_View]  chr11:90288942-90289025 [Contig_View]  MIR4490 [Vega]
ICGC DataPortalENSG00000266703
TCGA cBioPortalMIR4490
AceView (NCBI)MIR4490
Genatlas (Paris)MIR4490
WikiGenes100616186
SOURCE (Princeton)MIR4490
Genetics Home Reference (NIH)MIR4490
miRBaseMIR4490
dbDEMCMIR4490
Genomic and cartography
GoldenPath hg19 (UCSC)MIR4490  -     chr11:90288942-90289025 -  11q14.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIR4490  -     11q14.3   [Description]    (hg38-Dec_2013)
EnsemblMIR4490 - 11q14.3 [CytoView hg19]  MIR4490 - 11q14.3 [CytoView hg38]
Mapping of homologs : NCBIMIR4490 [Mapview hg19]  MIR4490 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000011 NC_018922 NT_033899 NW_004929380
Consensus coding sequences : CCDS (NCBI)MIR4490
Alternative Splicing GalleryENSG00000266703
Gene ExpressionMIR4490 [ NCBI-GEO ]   MIR4490 [ EBI - ARRAY_EXPRESS ]   MIR4490 [ SEEK ]   MIR4490 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4490 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616186
GTEX Portal (Tissue expression)MIR4490
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4490
DMDM Disease mutations100616186
Blocks (Seattle)MIR4490
Human Protein AtlasENSG00000266703
Protein Interaction databases
FunCoupENSG00000266703
BioGRIDMIR4490
STRING (EMBL)MIR4490
ZODIACMIR4490
Ontologies - Pathways
Huge Navigator MIR4490 [HugePedia]
snp3D : Map Gene to Disease100616186
BioCentury BCIQMIR4490
ClinGenMIR4490
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616186
Clinical trialMIR4490
Miscellaneous
canSAR (ICR)MIR4490 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4490
EVEXMIR4490
GoPubMedMIR4490
iHOPMIR4490
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 : Tue Mar 14 12:30:19 CET 2017

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