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MIR3916 (microRNA 3916)

Identity

Alias_symbol (synonym)hsa-mir-3916
Other aliasmir-3916
HGNC (Hugo) MIR3916
LocusID (NCBI) 100500849
Atlas_Id 69327
Location 1q44  [Link to chromosome band 1q44]
Location_base_pair Starts at 247201967 and ends at 247202060 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)MIR3916   38912
Cards
Entrez_Gene (NCBI)MIR3916  100500849  microRNA 3916
Aliasesmir-3916
GeneCards (Weizmann)MIR3916
Ensembl hg19 (Hinxton)ENSG00000263568 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000263568 [Gene_View]  chr1:247201967-247202060 [Contig_View]  MIR3916 [Vega]
ICGC DataPortalENSG00000263568
TCGA cBioPortalMIR3916
AceView (NCBI)MIR3916
Genatlas (Paris)MIR3916
WikiGenes100500849
SOURCE (Princeton)MIR3916
Genetics Home Reference (NIH)MIR3916
miRBaseMIR3916
dbDEMCMIR3916
Genomic and cartography
GoldenPath hg38 (UCSC)MIR3916  -     chr1:247201967-247202060 -  1q44   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR3916  -     1q44   [Description]    (hg19-Feb_2009)
EnsemblMIR3916 - 1q44 [CytoView hg19]  MIR3916 - 1q44 [CytoView hg38]
Mapping of homologs : NCBIMIR3916 [Mapview hg19]  MIR3916 [Mapview hg38]
Gene and transcription
Genbank (Entrez)LM611252
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR3916
Alternative Splicing GalleryENSG00000263568
Gene ExpressionMIR3916 [ NCBI-GEO ]   MIR3916 [ EBI - ARRAY_EXPRESS ]   MIR3916 [ SEEK ]   MIR3916 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR3916 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100500849
GTEX Portal (Tissue expression)MIR3916
Human Protein AtlasENSG00000263568-MIR3916 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR3916
DMDM Disease mutations100500849
Blocks (Seattle)MIR3916
Human Protein Atlas [tissue]ENSG00000263568-MIR3916 [tissue]
Protein Interaction databases
FunCoupENSG00000263568
BioGRIDMIR3916
STRING (EMBL)MIR3916
ZODIACMIR3916
Ontologies - Pathways
Huge Navigator MIR3916 [HugePedia]
snp3D : Map Gene to Disease100500849
BioCentury BCIQMIR3916
ClinGenMIR3916
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100500849
Clinical trialMIR3916
Miscellaneous
canSAR (ICR)MIR3916 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR3916
EVEXMIR3916
GoPubMedMIR3916
iHOPMIR3916
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 : Thu Nov 9 12:13:59 CET 2017

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