Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumours   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

MIR4474 (microRNA 4474)

Identity

Alias_symbol (synonym)hsa-mir-4474
Other alias-
HGNC (Hugo) MIR4474
LocusID (NCBI) 100616441
Atlas_Id 69486
Location 9p21.3  [Link to chromosome band 9p21]
Location_base_pair Starts at 20502263 and ends at 20502340 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)MIR4474   41821
Cards
Entrez_Gene (NCBI)MIR4474  100616441  microRNA 4474
Aliases
GeneCards (Weizmann)MIR4474
Ensembl hg19 (Hinxton) [Gene_View]  chr9:20502263-20502340 [Contig_View]  MIR4474 [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr9:20502263-20502340 [Contig_View]  MIR4474 [Vega]
TCGA cBioPortalMIR4474
AceView (NCBI)MIR4474
Genatlas (Paris)MIR4474
WikiGenes100616441
SOURCE (Princeton)MIR4474
Genetics Home Reference (NIH)MIR4474
miRBaseMIR4474
dbDEMCMIR4474
Genomic and cartography
GoldenPath hg19 (UCSC)MIR4474  -     chr9:20502263-20502340 -  9p21.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIR4474  -     9p21.3   [Description]    (hg38-Dec_2013)
EnsemblMIR4474 - 9p21.3 [CytoView hg19]  MIR4474 - 9p21.3 [CytoView hg38]
Mapping of homologs : NCBIMIR4474 [Mapview hg19]  MIR4474 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000009 NC_018920 NT_008413 NW_004929342
Consensus coding sequences : CCDS (NCBI)MIR4474
Gene ExpressionMIR4474 [ NCBI-GEO ]   MIR4474 [ EBI - ARRAY_EXPRESS ]   MIR4474 [ SEEK ]   MIR4474 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4474 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616441
GTEX Portal (Tissue expression)MIR4474
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4474
DMDM Disease mutations100616441
Blocks (Seattle)MIR4474
Protein Interaction databases
BioGRIDMIR4474
STRING (EMBL)MIR4474
ZODIACMIR4474
Ontologies - Pathways
Huge Navigator MIR4474 [HugePedia]
snp3D : Map Gene to Disease100616441
BioCentury BCIQMIR4474
ClinGenMIR4474
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616441
Clinical trialMIR4474
Miscellaneous
canSAR (ICR)MIR4474 (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4474
EVEXMIR4474
GoPubMedMIR4474
iHOPMIR4474
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 12:30:16 CET 2017

Home   Genes   Leukemias   Solid Tumours   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.