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MIR3689C (microRNA 3689c)

Identity

Alias_symbol (synonym)hsa-mir-3689c
Other alias-
HGNC (Hugo) MIR3689C
LocusID (NCBI) 100616333
Atlas_Id 69292
Location 9q34.3  [Link to chromosome band 9q34]
Location_base_pair Starts at 134849298 and ends at 134849369 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)MIR3689C   41816
Cards
Entrez_Gene (NCBI)MIR3689C  100616333  microRNA 3689c
Aliases
GeneCards (Weizmann)MIR3689C
Ensembl hg19 (Hinxton)ENSG00000264744 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000264744 [Gene_View]  chr9:134849298-134849369 [Contig_View]  MIR3689C [Vega]
ICGC DataPortalENSG00000264744
TCGA cBioPortalMIR3689C
AceView (NCBI)MIR3689C
Genatlas (Paris)MIR3689C
WikiGenes100616333
SOURCE (Princeton)MIR3689C
Genetics Home Reference (NIH)MIR3689C
miRBaseMIR3689C
dbDEMCMIR3689C
Genomic and cartography
GoldenPath hg38 (UCSC)MIR3689C  -     chr9:134849298-134849369 -  9q34.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR3689C  -     9q34.3   [Description]    (hg19-Feb_2009)
EnsemblMIR3689C - 9q34.3 [CytoView hg19]  MIR3689C - 9q34.3 [CytoView hg38]
Mapping of homologs : NCBIMIR3689C [Mapview hg19]  MIR3689C [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR3689C
Alternative Splicing GalleryENSG00000264744
Gene ExpressionMIR3689C [ NCBI-GEO ]   MIR3689C [ EBI - ARRAY_EXPRESS ]   MIR3689C [ SEEK ]   MIR3689C [ MEM ]
Gene Expression Viewer (FireBrowse)MIR3689C [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616333
GTEX Portal (Tissue expression)MIR3689C
Human Protein AtlasENSG00000264744-MIR3689C [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR3689C
DMDM Disease mutations100616333
Blocks (Seattle)MIR3689C
Human Protein Atlas [tissue]ENSG00000264744-MIR3689C [tissue]
Protein Interaction databases
FunCoupENSG00000264744
BioGRIDMIR3689C
STRING (EMBL)MIR3689C
ZODIACMIR3689C
Ontologies - Pathways
Huge Navigator MIR3689C [HugePedia]
snp3D : Map Gene to Disease100616333
BioCentury BCIQMIR3689C
ClinGenMIR3689C
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616333
Clinical trialMIR3689C
Miscellaneous
canSAR (ICR)MIR3689C (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR3689C
EVEXMIR3689C
GoPubMedMIR3689C
iHOPMIR3689C
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 Nov 21 13:20:09 CET 2017

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