Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

MIR4732 (microRNA 4732)

Identity

Alias_symbol (synonym)hsa-mir-4732
Other aliasmir-4732
HGNC (Hugo) MIR4732
LocusID (NCBI) 100616385
Atlas_Id 69645
Location 17q11.2  [Link to chromosome band 17q11]
Location_base_pair Starts at 28861655 and ends at 28861730 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)MIR4732   41639
Cards
Entrez_Gene (NCBI)MIR4732  100616385  microRNA 4732
Aliasesmir-4732
GeneCards (Weizmann)MIR4732
Ensembl hg19 (Hinxton)ENSG00000278521 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000278521 [Gene_View]  chr17:28861655-28861730 [Contig_View]  MIR4732 [Vega]
ICGC DataPortalENSG00000278521
TCGA cBioPortalMIR4732
AceView (NCBI)MIR4732
Genatlas (Paris)MIR4732
WikiGenes100616385
SOURCE (Princeton)MIR4732
Genetics Home Reference (NIH)MIR4732
miRBaseMIR4732
dbDEMCMIR4732
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4732  -     chr17:28861655-28861730 -  17q11.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4732  -     17q11.2   [Description]    (hg19-Feb_2009)
EnsemblMIR4732 - 17q11.2 [CytoView hg19]  MIR4732 - 17q11.2 [CytoView hg38]
Mapping of homologs : NCBIMIR4732 [Mapview hg19]  MIR4732 [Mapview hg38]
Gene and transcription
Genbank (Entrez)LM611398
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4732
Alternative Splicing GalleryENSG00000278521
Gene ExpressionMIR4732 [ NCBI-GEO ]   MIR4732 [ EBI - ARRAY_EXPRESS ]   MIR4732 [ SEEK ]   MIR4732 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4732 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616385
GTEX Portal (Tissue expression)MIR4732
Human Protein AtlasENSG00000278521-MIR4732 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4732
DMDM Disease mutations100616385
Blocks (Seattle)MIR4732
Human Protein Atlas [tissue]ENSG00000278521-MIR4732 [tissue]
Protein Interaction databases
FunCoupENSG00000278521
BioGRIDMIR4732
STRING (EMBL)MIR4732
ZODIACMIR4732
Ontologies - Pathways
Huge Navigator MIR4732 [HugePedia]
snp3D : Map Gene to Disease100616385
BioCentury BCIQMIR4732
ClinGenMIR4732
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616385
Clinical trialMIR4732
Miscellaneous
canSAR (ICR)MIR4732 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4732
EVEXMIR4732
GoPubMedMIR4732
iHOPMIR4732
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 : Thu Nov 9 12:15:11 CET 2017

Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.