Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumours   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

MIR4672 (microRNA 4672)

Identity

Alias_symbol (synonym)hsa-mir-4672
Other alias-
HGNC (Hugo) MIR4672
LocusID (NCBI) 100616429
Atlas_Id 69586
Location 9q34.11  [Link to chromosome band 9q34]
Location_base_pair Starts at 130631694 and ends at 130631774 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

DNA/RNA

 


External links

Nomenclature
HGNC (Hugo)MIR4672   41662
Cards
Entrez_Gene (NCBI)MIR4672  100616429  microRNA 4672
Aliases
GeneCards (Weizmann)MIR4672
Ensembl hg19 (Hinxton) [Gene_View]  chr9:130631694-130631774 [Contig_View]  MIR4672 [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr9:130631694-130631774 [Contig_View]  MIR4672 [Vega]
TCGA cBioPortalMIR4672
AceView (NCBI)MIR4672
Genatlas (Paris)MIR4672
WikiGenes100616429
SOURCE (Princeton)MIR4672
Genetics Home Reference (NIH)MIR4672
miRBaseMIR4672
dbDEMCMIR4672
Genomic and cartography
GoldenPath hg19 (UCSC)MIR4672  -     chr9:130631694-130631774 -  9q34.11   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIR4672  -     9q34.11   [Description]    (hg38-Dec_2013)
EnsemblMIR4672 - 9q34.11 [CytoView hg19]  MIR4672 - 9q34.11 [CytoView hg38]
Mapping of homologs : NCBIMIR4672 [Mapview hg19]  MIR4672 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000009 NC_018920 NT_008470 NW_004929366
Consensus coding sequences : CCDS (NCBI)MIR4672
Gene ExpressionMIR4672 [ NCBI-GEO ]   MIR4672 [ EBI - ARRAY_EXPRESS ]   MIR4672 [ SEEK ]   MIR4672 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4672 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616429
GTEX Portal (Tissue expression)MIR4672
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4672
DMDM Disease mutations100616429
Blocks (Seattle)MIR4672
Protein Interaction databases
BioGRIDMIR4672
STRING (EMBL)MIR4672
ZODIACMIR4672
Ontologies - Pathways
Huge Navigator MIR4672 [HugePedia]
snp3D : Map Gene to Disease100616429
BioCentury BCIQMIR4672
ClinGenMIR4672
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616429
Clinical trialMIR4672
Miscellaneous
canSAR (ICR)MIR4672 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4672
EVEXMIR4672
GoPubMedMIR4672
iHOPMIR4672
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 12:30:41 CET 2017

Home   Genes   Leukemias   Solid Tumours   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.