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

MIR4666B (microRNA 4666b)

Identity

Alias_symbol (synonym)hsa-mir-4666b
Other alias-
HGNC (Hugo) MIR4666B
LocusID (NCBI) 100847047
Atlas_Id 76535
Location Xp21.2  [Link to chromosome band Xp21]
Location_base_pair Starts at 29574278 and ends at 29574358 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)MIR4666B   43486
Cards
Entrez_Gene (NCBI)MIR4666B  100847047  microRNA 4666b
Aliases
GeneCards (Weizmann)MIR4666B
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chrX:29574278-29574358 [Contig_View]  MIR4666B [Vega]
TCGA cBioPortalMIR4666B
AceView (NCBI)MIR4666B
Genatlas (Paris)MIR4666B
WikiGenes100847047
SOURCE (Princeton)MIR4666B
Genetics Home Reference (NIH)MIR4666B
miRBaseMIR4666B
dbDEMCMIR4666B
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4666B  -     chrX:29574278-29574358 +  Xp21.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4666B  -     Xp21.2   [Description]    (hg19-Feb_2009)
EnsemblMIR4666B - Xp21.2 [CytoView hg19]  MIR4666B - Xp21.2 [CytoView hg38]
Mapping of homologs : NCBIMIR4666B [Mapview hg19]  MIR4666B [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4666B
Gene ExpressionMIR4666B [ NCBI-GEO ]   MIR4666B [ EBI - ARRAY_EXPRESS ]   MIR4666B [ SEEK ]   MIR4666B [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4666B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100847047
GTEX Portal (Tissue expression)MIR4666B
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4666B
DMDM Disease mutations100847047
Blocks (Seattle)MIR4666B
Protein Interaction databases
BioGRIDMIR4666B
STRING (EMBL)MIR4666B
ZODIACMIR4666B
Ontologies - Pathways
Huge Navigator MIR4666B [HugePedia]
snp3D : Map Gene to Disease100847047
BioCentury BCIQMIR4666B
ClinGenMIR4666B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100847047
Clinical trialMIR4666B
Miscellaneous
canSAR (ICR)MIR4666B (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4666B
EVEXMIR4666B
GoPubMedMIR4666B
iHOPMIR4666B
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 14:00:05 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.