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

MIR891A (microRNA 891a)

Identity

Alias_namesMIRN891A
Alias_symbol (synonym)hsa-mir-891a
Other alias
HGNC (Hugo) MIR891A
LocusID (NCBI) 100126341
Atlas_Id 70298
Location Xq27.3  [Link to chromosome band Xq27]
Location_base_pair Starts at 146027794 and ends at 146027872 bp from pter ( according to hg38-Dec_2013)

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)MIR891A   33635
Cards
Entrez_Gene (NCBI)MIR891A  100126341  microRNA 891a
AliasesMIRN891A
GeneCards (Weizmann)MIR891A
Ensembl hg19 (Hinxton)ENSG00000216056 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000216056 [Gene_View]  chrX:146027794-146027872 [Contig_View]  MIR891A [Vega]
ICGC DataPortalENSG00000216056
TCGA cBioPortalMIR891A
AceView (NCBI)MIR891A
Genatlas (Paris)MIR891A
WikiGenes100126341
SOURCE (Princeton)MIR891A
Genetics Home Reference (NIH)MIR891A
miRBaseMIR891A
dbDEMCMIR891A
Genomic and cartography
GoldenPath hg38 (UCSC)MIR891A  -     chrX:146027794-146027872 -  Xq27.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR891A  -     Xq27.3   [Description]    (hg19-Feb_2009)
EnsemblMIR891A - Xq27.3 [CytoView hg19]  MIR891A - Xq27.3 [CytoView hg38]
Mapping of homologs : NCBIMIR891A [Mapview hg19]  MIR891A [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR891A
Alternative Splicing GalleryENSG00000216056
Gene ExpressionMIR891A [ NCBI-GEO ]   MIR891A [ EBI - ARRAY_EXPRESS ]   MIR891A [ SEEK ]   MIR891A [ MEM ]
Gene Expression Viewer (FireBrowse)MIR891A [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100126341
GTEX Portal (Tissue expression)MIR891A
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR891A
DMDM Disease mutations100126341
Blocks (Seattle)MIR891A
Human Protein AtlasENSG00000216056
Protein Interaction databases
FunCoupENSG00000216056
BioGRIDMIR891A
STRING (EMBL)MIR891A
ZODIACMIR891A
Ontologies - Pathways
Huge Navigator MIR891A [HugePedia]
snp3D : Map Gene to Disease100126341
BioCentury BCIQMIR891A
ClinGenMIR891A
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100126341
Chemical/Pharm GKB GenePA164722991
Clinical trialMIR891A
Miscellaneous
canSAR (ICR)MIR891A (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR891A
EVEXMIR891A
GoPubMedMIR891A
iHOPMIR891A
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 : Fri May 19 11:43:16 CEST 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.