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MIR4432 (microRNA 4432)

Identity

Alias_symbol (synonym)hsa-mir-4432
Other alias-
HGNC (Hugo) MIR4432
LocusID (NCBI) 100616473
Atlas_Id 69446
Location 2p16.1  [Link to chromosome band 2p16]
Location_base_pair Starts at 60387362 and ends at 60387445 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)MIR4432   41649
Cards
Entrez_Gene (NCBI)MIR4432  100616473  microRNA 4432
Aliases
GeneCards (Weizmann)MIR4432
Ensembl hg19 (Hinxton)ENSG00000266078 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000266078 [Gene_View]  chr2:60387362-60387445 [Contig_View]  MIR4432 [Vega]
ICGC DataPortalENSG00000266078
TCGA cBioPortalMIR4432
AceView (NCBI)MIR4432
Genatlas (Paris)MIR4432
WikiGenes100616473
SOURCE (Princeton)MIR4432
Genetics Home Reference (NIH)MIR4432
miRBaseMIR4432
dbDEMCMIR4432
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4432  -     chr2:60387362-60387445 -  2p16.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4432  -     2p16.1   [Description]    (hg19-Feb_2009)
EnsemblMIR4432 - 2p16.1 [CytoView hg19]  MIR4432 - 2p16.1 [CytoView hg38]
Mapping of homologs : NCBIMIR4432 [Mapview hg19]  MIR4432 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4432
Alternative Splicing GalleryENSG00000266078
Gene ExpressionMIR4432 [ NCBI-GEO ]   MIR4432 [ EBI - ARRAY_EXPRESS ]   MIR4432 [ SEEK ]   MIR4432 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4432 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616473
GTEX Portal (Tissue expression)MIR4432
Human Protein AtlasENSG00000266078-MIR4432 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4432
DMDM Disease mutations100616473
Blocks (Seattle)MIR4432
Human Protein Atlas [tissue]ENSG00000266078-MIR4432 [tissue]
Protein Interaction databases
FunCoupENSG00000266078
BioGRIDMIR4432
STRING (EMBL)MIR4432
ZODIACMIR4432
Ontologies - Pathways
Huge Navigator MIR4432 [HugePedia]
snp3D : Map Gene to Disease100616473
BioCentury BCIQMIR4432
ClinGenMIR4432
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616473
Clinical trialMIR4432
Miscellaneous
canSAR (ICR)MIR4432 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4432
EVEXMIR4432
GoPubMedMIR4432
iHOPMIR4432
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Thu Nov 9 12:14:26 CET 2017

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