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MIR4477B (microRNA 4477b)

Identity

Alias_symbol (synonym)hsa-mir-4477b
Other alias-
HGNC (Hugo) MIR4477B
LocusID (NCBI) 100616194
Atlas_Id 76970
Location 9q13  [Link to chromosome band 9q13]
Location_base_pair Starts at 68415308 and ends at 68415388 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)MIR4477B   41898
Cards
Entrez_Gene (NCBI)MIR4477B  100616194  microRNA 4477b
Aliases
GeneCards (Weizmann)MIR4477B
Ensembl hg19 (Hinxton)ENSG00000266017 [Gene_View]  chr9:68415308-68415388 [Contig_View]  MIR4477B [Vega]
Ensembl hg38 (Hinxton)ENSG00000266017 [Gene_View]  chr9:68415308-68415388 [Contig_View]  MIR4477B [Vega]
ICGC DataPortalENSG00000266017
TCGA cBioPortalMIR4477B
AceView (NCBI)MIR4477B
Genatlas (Paris)MIR4477B
WikiGenes100616194
SOURCE (Princeton)MIR4477B
Genetics Home Reference (NIH)MIR4477B
miRBaseMIR4477B
dbDEMCMIR4477B
Genomic and cartography
GoldenPath hg19 (UCSC)MIR4477B  -     chr9:68415308-68415388 +  9q13   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIR4477B  -     9q13   [Description]    (hg38-Dec_2013)
EnsemblMIR4477B - 9q13 [CytoView hg19]  MIR4477B - 9q13 [CytoView hg38]
Mapping of homologs : NCBIMIR4477B [Mapview hg19]  MIR4477B [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000009 NC_018920 NT_078067 NW_004929359
Consensus coding sequences : CCDS (NCBI)MIR4477B
Alternative Splicing GalleryENSG00000266017
Gene ExpressionMIR4477B [ NCBI-GEO ]   MIR4477B [ EBI - ARRAY_EXPRESS ]   MIR4477B [ SEEK ]   MIR4477B [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4477B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616194
GTEX Portal (Tissue expression)MIR4477B
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4477B
DMDM Disease mutations100616194
Blocks (Seattle)MIR4477B
Human Protein AtlasENSG00000266017
Protein Interaction databases
FunCoupENSG00000266017
BioGRIDMIR4477B
STRING (EMBL)MIR4477B
ZODIACMIR4477B
Ontologies - Pathways
Huge Navigator MIR4477B [HugePedia]
snp3D : Map Gene to Disease100616194
BioCentury BCIQMIR4477B
ClinGenMIR4477B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616194
Clinical trialMIR4477B
Miscellaneous
canSAR (ICR)MIR4477B (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4477B
EVEXMIR4477B
GoPubMedMIR4477B
iHOPMIR4477B
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 12:30:17 CET 2017

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