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MIR3912 (microRNA 3912)

Identity

Alias_symbol (synonym)hsa-mir-3912
Other aliasmir-3912
HGNC (Hugo) MIR3912
LocusID (NCBI) 100500831
Atlas_Id 69322
Location 5q35.1  [Link to chromosome band 5q35]
Location_base_pair Starts at 171386656 and ends at 171386760 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)MIR3912   38923
Cards
Entrez_Gene (NCBI)MIR3912  100500831  microRNA 3912
Aliasesmir-3912
GeneCards (Weizmann)MIR3912
Ensembl hg19 (Hinxton)ENSG00000264249 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000264249 [Gene_View]  chr5:171386656-171386760 [Contig_View]  MIR3912 [Vega]
ICGC DataPortalENSG00000264249
TCGA cBioPortalMIR3912
AceView (NCBI)MIR3912
Genatlas (Paris)MIR3912
WikiGenes100500831
SOURCE (Princeton)MIR3912
Genetics Home Reference (NIH)MIR3912
miRBaseMIR3912
dbDEMCMIR3912
Genomic and cartography
GoldenPath hg38 (UCSC)MIR3912  -     chr5:171386656-171386760 -  5q35.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR3912  -     5q35.1   [Description]    (hg19-Feb_2009)
EnsemblMIR3912 - 5q35.1 [CytoView hg19]  MIR3912 - 5q35.1 [CytoView hg38]
Mapping of homologs : NCBIMIR3912 [Mapview hg19]  MIR3912 [Mapview hg38]
Gene and transcription
Genbank (Entrez)LM611248
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR3912
Alternative Splicing GalleryENSG00000264249
Gene ExpressionMIR3912 [ NCBI-GEO ]   MIR3912 [ EBI - ARRAY_EXPRESS ]   MIR3912 [ SEEK ]   MIR3912 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR3912 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100500831
GTEX Portal (Tissue expression)MIR3912
Human Protein AtlasENSG00000264249-MIR3912 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR3912
DMDM Disease mutations100500831
Blocks (Seattle)MIR3912
Human Protein Atlas [tissue]ENSG00000264249-MIR3912 [tissue]
Protein Interaction databases
FunCoupENSG00000264249
BioGRIDMIR3912
STRING (EMBL)MIR3912
ZODIACMIR3912
Ontologies - Pathways
Huge Navigator MIR3912 [HugePedia]
snp3D : Map Gene to Disease100500831
BioCentury BCIQMIR3912
ClinGenMIR3912
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100500831
Clinical trialMIR3912
Miscellaneous
canSAR (ICR)MIR3912 (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR3912
EVEXMIR3912
GoPubMedMIR3912
iHOPMIR3912
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Tue Nov 21 13:12:23 CET 2017

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