Atlas of Genetics and Cytogenetics in Oncology and Haematology


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MIR4433B (microRNA 4433b)

Identity

Alias_symbol (synonym)hsa-mir-4433b
Other alias
HGNC (Hugo) MIR4433B
LocusID (NCBI) 102465833
Atlas_Id 77461
Location 2p14  [Link to chromosome band 2p14]
Location_base_pair Starts at 64340747 and ends at 64340848 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)MIR4433B   50258
Cards
Entrez_Gene (NCBI)MIR4433B  102465833  microRNA 4433b
Aliaseshsa-mir-4433b
GeneCards (Weizmann)MIR4433B
Ensembl hg19 (Hinxton)ENSG00000264297 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000264297 [Gene_View]  chr2:64340747-64340848 [Contig_View]  MIR4433B [Vega]
ICGC DataPortalENSG00000264297
TCGA cBioPortalMIR4433B
AceView (NCBI)MIR4433B
Genatlas (Paris)MIR4433B
WikiGenes102465833
SOURCE (Princeton)MIR4433B
Genetics Home Reference (NIH)MIR4433B
miRBaseMIR4433B
dbDEMCMIR4433B
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4433B  -     chr2:64340747-64340848 -  2p14   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4433B  -     2p14   [Description]    (hg19-Feb_2009)
EnsemblMIR4433B - 2p14 [CytoView hg19]  MIR4433B - 2p14 [CytoView hg38]
Mapping of homologs : NCBIMIR4433B [Mapview hg19]  MIR4433B [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4433B
Alternative Splicing GalleryENSG00000264297
Gene ExpressionMIR4433B [ NCBI-GEO ]   MIR4433B [ EBI - ARRAY_EXPRESS ]   MIR4433B [ SEEK ]   MIR4433B [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4433B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)102465833
GTEX Portal (Tissue expression)MIR4433B
Human Protein AtlasENSG00000264297-MIR4433B [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4433B
DMDM Disease mutations102465833
Blocks (Seattle)MIR4433B
Human Protein Atlas [tissue]ENSG00000264297-MIR4433B [tissue]
Protein Interaction databases
FunCoupENSG00000264297
BioGRIDMIR4433B
STRING (EMBL)MIR4433B
ZODIACMIR4433B
Ontologies - Pathways
Huge Navigator MIR4433B [HugePedia]
snp3D : Map Gene to Disease102465833
BioCentury BCIQMIR4433B
ClinGenMIR4433B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD102465833
Clinical trialMIR4433B
Miscellaneous
canSAR (ICR)MIR4433B (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4433B
EVEXMIR4433B
GoPubMedMIR4433B
iHOPMIR4433B
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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