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MIR3649 (microRNA 3649)

Identity

Alias_symbol (synonym)hsa-mir-3649
Other alias-
HGNC (Hugo) MIR3649
LocusID (NCBI) 100500816
Atlas_Id 69258
Location 12p13.33  [Link to chromosome band 12p13]
Location_base_pair Starts at 1769481 and ends at 1769546 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)MIR3649   38948
Cards
Entrez_Gene (NCBI)MIR3649  100500816  microRNA 3649
Aliases
GeneCards (Weizmann)MIR3649
Ensembl hg19 (Hinxton)ENSG00000266043 [Gene_View]  chr12:1769481-1769546 [Contig_View]  MIR3649 [Vega]
Ensembl hg38 (Hinxton)ENSG00000266043 [Gene_View]  chr12:1769481-1769546 [Contig_View]  MIR3649 [Vega]
ICGC DataPortalENSG00000266043
TCGA cBioPortalMIR3649
AceView (NCBI)MIR3649
Genatlas (Paris)MIR3649
WikiGenes100500816
SOURCE (Princeton)MIR3649
Genetics Home Reference (NIH)MIR3649
miRBaseMIR3649
dbDEMCMIR3649
Genomic and cartography
GoldenPath hg19 (UCSC)MIR3649  -     chr12:1769481-1769546 -  12p13.33   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIR3649  -     12p13.33   [Description]    (hg38-Dec_2013)
EnsemblMIR3649 - 12p13.33 [CytoView hg19]  MIR3649 - 12p13.33 [CytoView hg38]
Mapping of homologs : NCBIMIR3649 [Mapview hg19]  MIR3649 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000012 NC_018923 NT_009759 NW_004929382
Consensus coding sequences : CCDS (NCBI)MIR3649
Alternative Splicing GalleryENSG00000266043
Gene ExpressionMIR3649 [ NCBI-GEO ]   MIR3649 [ EBI - ARRAY_EXPRESS ]   MIR3649 [ SEEK ]   MIR3649 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR3649 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100500816
GTEX Portal (Tissue expression)MIR3649
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR3649
DMDM Disease mutations100500816
Blocks (Seattle)MIR3649
Human Protein AtlasENSG00000266043
Protein Interaction databases
FunCoupENSG00000266043
BioGRIDMIR3649
STRING (EMBL)MIR3649
ZODIACMIR3649
Ontologies - Pathways
Huge Navigator MIR3649 [HugePedia]
snp3D : Map Gene to Disease100500816
BioCentury BCIQMIR3649
ClinGenMIR3649
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100500816
Clinical trialMIR3649
Miscellaneous
canSAR (ICR)MIR3649 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR3649
EVEXMIR3649
GoPubMedMIR3649
iHOPMIR3649
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 : Tue Mar 14 12:29:20 CET 2017

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