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MIR4662B (microRNA 4662b)

Identity

Alias_symbol (synonym)hsa-mir-4662b
Other alias-
HGNC (Hugo) MIR4662B
LocusID (NCBI) 100616255
Atlas_Id 77018
Location 8q24.13  [Link to chromosome band 8q24]
Location_base_pair Starts at 125834220 and ends at 125834300 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


External links

Nomenclature
HGNC (Hugo)MIR4662B   41607
Cards
Entrez_Gene (NCBI)MIR4662B  100616255  microRNA 4662b
Aliases
GeneCards (Weizmann)MIR4662B
Ensembl hg19 (Hinxton)ENSG00000263735 [Gene_View]  chr8:125834220-125834300 [Contig_View]  MIR4662B [Vega]
Ensembl hg38 (Hinxton)ENSG00000263735 [Gene_View]  chr8:125834220-125834300 [Contig_View]  MIR4662B [Vega]
ICGC DataPortalENSG00000263735
TCGA cBioPortalMIR4662B
AceView (NCBI)MIR4662B
Genatlas (Paris)MIR4662B
WikiGenes100616255
SOURCE (Princeton)MIR4662B
Genetics Home Reference (NIH)MIR4662B
miRBaseMIR4662B
dbDEMCMIR4662B
Genomic and cartography
GoldenPath hg19 (UCSC)MIR4662B  -     chr8:125834220-125834300 -  8q24.13   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIR4662B  -     8q24.13   [Description]    (hg38-Dec_2013)
EnsemblMIR4662B - 8q24.13 [CytoView hg19]  MIR4662B - 8q24.13 [CytoView hg38]
Mapping of homologs : NCBIMIR4662B [Mapview hg19]  MIR4662B [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000008 NC_018919 NT_008046 NW_004929340
Consensus coding sequences : CCDS (NCBI)MIR4662B
Alternative Splicing GalleryENSG00000263735
Gene ExpressionMIR4662B [ NCBI-GEO ]   MIR4662B [ EBI - ARRAY_EXPRESS ]   MIR4662B [ SEEK ]   MIR4662B [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4662B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616255
GTEX Portal (Tissue expression)MIR4662B
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4662B
DMDM Disease mutations100616255
Blocks (Seattle)MIR4662B
Human Protein AtlasENSG00000263735
Protein Interaction databases
FunCoupENSG00000263735
BioGRIDMIR4662B
STRING (EMBL)MIR4662B
ZODIACMIR4662B
Ontologies - Pathways
Huge Navigator MIR4662B [HugePedia]
snp3D : Map Gene to Disease100616255
BioCentury BCIQMIR4662B
ClinGenMIR4662B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616255
Clinical trialMIR4662B
Miscellaneous
canSAR (ICR)MIR4662B (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4662B
EVEXMIR4662B
GoPubMedMIR4662B
iHOPMIR4662B
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

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indexed on : Tue Mar 14 12:30:39 CET 2017

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