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MIR4752 (microRNA 4752)

Identity

Alias_symbol (synonym)hsa-mir-4752
Other alias-
HGNC (Hugo) MIR4752
LocusID (NCBI) 100616171
Atlas_Id 69665
Location 19q13.42  [Link to chromosome band 19q13]
Location_base_pair Starts at 54785964 and ends at 54786035 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)MIR4752   41803
Cards
Entrez_Gene (NCBI)MIR4752  100616171  microRNA 4752
Aliases
GeneCards (Weizmann)MIR4752
Ensembl hg19 (Hinxton)ENSG00000264703 [Gene_View]  chr19:54785964-54786035 [Contig_View]  MIR4752 [Vega]
Ensembl hg38 (Hinxton)ENSG00000264703 [Gene_View]  chr19:54785964-54786035 [Contig_View]  MIR4752 [Vega]
ICGC DataPortalENSG00000264703
TCGA cBioPortalMIR4752
AceView (NCBI)MIR4752
Genatlas (Paris)MIR4752
WikiGenes100616171
SOURCE (Princeton)MIR4752
Genetics Home Reference (NIH)MIR4752
miRBaseMIR4752
dbDEMCMIR4752
Genomic and cartography
GoldenPath hg19 (UCSC)MIR4752  -     chr19:54785964-54786035 +  19q13.42   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIR4752  -     19q13.42   [Description]    (hg38-Dec_2013)
EnsemblMIR4752 - 19q13.42 [CytoView hg19]  MIR4752 - 19q13.42 [CytoView hg38]
Mapping of homologs : NCBIMIR4752 [Mapview hg19]  MIR4752 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000019 NC_018930 NT_011109 NT_187693 NW_003571054 NW_003571055 NW_003571061 NW_004929415
Consensus coding sequences : CCDS (NCBI)MIR4752
Alternative Splicing GalleryENSG00000264703
Gene ExpressionMIR4752 [ NCBI-GEO ]   MIR4752 [ EBI - ARRAY_EXPRESS ]   MIR4752 [ SEEK ]   MIR4752 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4752 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616171
GTEX Portal (Tissue expression)MIR4752
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4752
DMDM Disease mutations100616171
Blocks (Seattle)MIR4752
Human Protein AtlasENSG00000264703
Protein Interaction databases
FunCoupENSG00000264703
BioGRIDMIR4752
STRING (EMBL)MIR4752
ZODIACMIR4752
Ontologies - Pathways
Huge Navigator MIR4752 [HugePedia]
snp3D : Map Gene to Disease100616171
BioCentury BCIQMIR4752
ClinGenMIR4752
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616171
Clinical trialMIR4752
Miscellaneous
canSAR (ICR)MIR4752 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4752
EVEXMIR4752
GoPubMedMIR4752
iHOPMIR4752
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 12:30:58 CET 2017

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