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MIR3925 (microRNA 3925)

Identity

Alias_symbol (synonym)hsa-mir-3925
Other alias-
HGNC (Hugo) MIR3925
LocusID (NCBI) 100500885
Atlas_Id 69335
Location 6p21.2  [Link to chromosome band 6p21]
Location_base_pair Starts at 36622436 and ends at 36622512 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)MIR3925   38996
Cards
Entrez_Gene (NCBI)MIR3925  100500885  microRNA 3925
Aliases
GeneCards (Weizmann)MIR3925
Ensembl hg19 (Hinxton)ENSG00000263894 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000263894 [Gene_View]  ENSG00000263894 [Sequence]  chr6:36622436-36622512 [Contig_View]  MIR3925 [Vega]
ICGC DataPortalENSG00000263894
TCGA cBioPortalMIR3925
AceView (NCBI)MIR3925
Genatlas (Paris)MIR3925
WikiGenes100500885
SOURCE (Princeton)MIR3925
Genetics Home Reference (NIH)MIR3925
miRBaseMIR3925
dbDEMCMIR3925
Genomic and cartography
GoldenPath hg38 (UCSC)MIR3925  -     chr6:36622436-36622512 -  6p21.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR3925  -     6p21.2   [Description]    (hg19-Feb_2009)
EnsemblMIR3925 - 6p21.2 [CytoView hg19]  MIR3925 - 6p21.2 [CytoView hg38]
Mapping of homologs : NCBIMIR3925 [Mapview hg19]  MIR3925 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR3925
Alternative Splicing GalleryENSG00000263894
Gene ExpressionMIR3925 [ NCBI-GEO ]   MIR3925 [ EBI - ARRAY_EXPRESS ]   MIR3925 [ SEEK ]   MIR3925 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR3925 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100500885
GTEX Portal (Tissue expression)MIR3925
Human Protein AtlasENSG00000263894-MIR3925 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR3925
DMDM Disease mutations100500885
Blocks (Seattle)MIR3925
Human Protein Atlas [tissue]ENSG00000263894-MIR3925 [tissue]
Protein Interaction databases
FunCoupENSG00000263894
BioGRIDMIR3925
STRING (EMBL)MIR3925
ZODIACMIR3925
Ontologies - Pathways
Huge Navigator MIR3925 [HugePedia]
snp3D : Map Gene to Disease100500885
BioCentury BCIQMIR3925
ClinGenMIR3925
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100500885
Clinical trialMIR3925
Miscellaneous
canSAR (ICR)MIR3925 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR3925
EVEXMIR3925
GoPubMedMIR3925
iHOPMIR3925
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 : Mon Jul 30 14:14:11 CEST 2018

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