Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumors   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

MIR4291 (microRNA 4291)

Identity

Alias_symbol (synonym)hsa-mir-4291
Other alias-
HGNC (Hugo) MIR4291
LocusID (NCBI) 100422927
Atlas_Id 69397
Location 9q22.31  [Link to chromosome band 9q22]
Location_base_pair Starts at 93819357 and ends at 93819421 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)MIR4291   38267
Cards
Entrez_Gene (NCBI)MIR4291  100422927  microRNA 4291
Aliases
GeneCards (Weizmann)MIR4291
Ensembl hg19 (Hinxton)ENSG00000265347 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000265347 [Gene_View]  chr9:93819357-93819421 [Contig_View]  MIR4291 [Vega]
ICGC DataPortalENSG00000265347
TCGA cBioPortalMIR4291
AceView (NCBI)MIR4291
Genatlas (Paris)MIR4291
WikiGenes100422927
SOURCE (Princeton)MIR4291
Genetics Home Reference (NIH)MIR4291
miRBaseMIR4291
dbDEMCMIR4291
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4291  -     chr9:93819357-93819421 +  9q22.31   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4291  -     9q22.31   [Description]    (hg19-Feb_2009)
EnsemblMIR4291 - 9q22.31 [CytoView hg19]  MIR4291 - 9q22.31 [CytoView hg38]
Mapping of homologs : NCBIMIR4291 [Mapview hg19]  MIR4291 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4291
Alternative Splicing GalleryENSG00000265347
Gene ExpressionMIR4291 [ NCBI-GEO ]   MIR4291 [ EBI - ARRAY_EXPRESS ]   MIR4291 [ SEEK ]   MIR4291 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4291 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100422927
GTEX Portal (Tissue expression)MIR4291
Human Protein AtlasENSG00000265347-MIR4291 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4291
DMDM Disease mutations100422927
Blocks (Seattle)MIR4291
Human Protein Atlas [tissue]ENSG00000265347-MIR4291 [tissue]
Protein Interaction databases
FunCoupENSG00000265347
BioGRIDMIR4291
STRING (EMBL)MIR4291
ZODIACMIR4291
Ontologies - Pathways
Huge Navigator MIR4291 [HugePedia]
snp3D : Map Gene to Disease100422927
BioCentury BCIQMIR4291
ClinGenMIR4291
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100422927
Chemical/Pharm GKB GenePA165585862
Clinical trialMIR4291
Miscellaneous
canSAR (ICR)MIR4291 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4291
EVEXMIR4291
GoPubMedMIR4291
iHOPMIR4291
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 : Thu Nov 9 12:14:15 CET 2017

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

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.