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

MIR2278 (microRNA 2278)

Identity

Alias_symbol (synonym)hsa-mir-2278
Other aliasmir-2278
HGNC (Hugo) MIR2278
LocusID (NCBI) 100313780
Atlas_Id 55661
Location 9q22.32  [Link to chromosome band 9q22]
Location_base_pair Starts at 97572244 and ends at 97572339 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)MIR2278   37315
Cards
Entrez_Gene (NCBI)MIR2278  100313780  microRNA 2278
Aliasesmir-2278
GeneCards (Weizmann)MIR2278
Ensembl hg19 (Hinxton)ENSG00000252153 [Gene_View]  chr9:97572244-97572339 [Contig_View]  MIR2278 [Vega]
Ensembl hg38 (Hinxton)ENSG00000252153 [Gene_View]  chr9:97572244-97572339 [Contig_View]  MIR2278 [Vega]
ICGC DataPortalENSG00000252153
TCGA cBioPortalMIR2278
AceView (NCBI)MIR2278
Genatlas (Paris)MIR2278
WikiGenes100313780
SOURCE (Princeton)MIR2278
Genetics Home Reference (NIH)MIR2278
miRBaseMIR2278
dbDEMCMIR2278
Genomic and cartography
GoldenPath hg19 (UCSC)MIR2278  -     chr9:97572244-97572339 +  9q22.32   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIR2278  -     9q22.32   [Description]    (hg38-Dec_2013)
EnsemblMIR2278 - 9q22.32 [CytoView hg19]  MIR2278 - 9q22.32 [CytoView hg38]
Mapping of homologs : NCBIMIR2278 [Mapview hg19]  MIR2278 [Mapview hg38]
Gene and transcription
Genbank (Entrez)LM610743
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000009 NC_018920 NT_008470 NW_004929366
Consensus coding sequences : CCDS (NCBI)MIR2278
Alternative Splicing GalleryENSG00000252153
Gene ExpressionMIR2278 [ NCBI-GEO ]   MIR2278 [ EBI - ARRAY_EXPRESS ]   MIR2278 [ SEEK ]   MIR2278 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR2278 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100313780
GTEX Portal (Tissue expression)MIR2278
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR2278
DMDM Disease mutations100313780
Blocks (Seattle)MIR2278
Human Protein AtlasENSG00000252153
Protein Interaction databases
FunCoupENSG00000252153
BioGRIDMIR2278
STRING (EMBL)MIR2278
ZODIACMIR2278
Ontologies - Pathways
Huge Navigator MIR2278 [HugePedia]
snp3D : Map Gene to Disease100313780
BioCentury BCIQMIR2278
ClinGenMIR2278
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100313780
Chemical/Pharm GKB GenePA165585838
Clinical trialMIR2278
Miscellaneous
canSAR (ICR)MIR2278 (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR2278
EVEXMIR2278
GoPubMedMIR2278
iHOPMIR2278
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 Mar 30 15:09:42 CEST 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.