Atlas of Genetics and Cytogenetics in Oncology and Haematology


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MIR3179-1 (microRNA 3179-1)

Identity

Alias_symbol (synonym)hsa-mir-3179-1
Other alias-
HGNC (Hugo) MIR3179-1
LocusID (NCBI) 100422960
Atlas_Id 69194
Location 16p13.11  [Link to chromosome band 16p13]
Location_base_pair Starts at 14995365 and ends at 14995448 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)MIR3179-1   38353
Cards
Entrez_Gene (NCBI)MIR3179-1  100422960  microRNA 3179-1
Aliases
GeneCards (Weizmann)MIR3179-1
Ensembl hg19 (Hinxton)ENSG00000274301 [Gene_View]  chr16:14995365-14995448 [Contig_View]  MIR3179-1 [Vega]
Ensembl hg38 (Hinxton)ENSG00000274301 [Gene_View]  chr16:14995365-14995448 [Contig_View]  MIR3179-1 [Vega]
ICGC DataPortalENSG00000274301
TCGA cBioPortalMIR3179-1
AceView (NCBI)MIR3179-1
Genatlas (Paris)MIR3179-1
WikiGenes100422960
SOURCE (Princeton)MIR3179-1
Genetics Home Reference (NIH)MIR3179-1
miRBaseMIR3179-1
dbDEMCMIR3179-1
Genomic and cartography
GoldenPath hg19 (UCSC)MIR3179-1  -     chr16:14995365-14995448 +  16p13.11   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIR3179-1  -     16p13.11   [Description]    (hg38-Dec_2013)
EnsemblMIR3179-1 - 16p13.11 [CytoView hg19]  MIR3179-1 - 16p13.11 [CytoView hg38]
Mapping of homologs : NCBIMIR3179-1 [Mapview hg19]  MIR3179-1 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000016 NC_018927 NT_010393 NT_187607 NW_004929400
Consensus coding sequences : CCDS (NCBI)MIR3179-1
Alternative Splicing GalleryENSG00000274301
Gene ExpressionMIR3179-1 [ NCBI-GEO ]   MIR3179-1 [ EBI - ARRAY_EXPRESS ]   MIR3179-1 [ SEEK ]   MIR3179-1 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR3179-1 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100422960
GTEX Portal (Tissue expression)MIR3179-1
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR3179-1
DMDM Disease mutations100422960
Blocks (Seattle)MIR3179-1
Human Protein AtlasENSG00000274301
Protein Interaction databases
FunCoupENSG00000274301
BioGRIDMIR3179-1
STRING (EMBL)MIR3179-1
ZODIACMIR3179-1
Ontologies - Pathways
Huge Navigator MIR3179-1 [HugePedia]
snp3D : Map Gene to Disease100422960
BioCentury BCIQMIR3179-1
ClinGenMIR3179-1
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100422960
Chemical/Pharm GKB GenePA165450173
Clinical trialMIR3179-1
Miscellaneous
canSAR (ICR)MIR3179-1 (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR3179-1
EVEXMIR3179-1
GoPubMedMIR3179-1
iHOPMIR3179-1
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Mar 14 12:29:08 CET 2017

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