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

MIR4632 (microRNA 4632)

Identity

Alias_symbol (synonym)hsa-mir-4632
Other alias-
HGNC (Hugo) MIR4632
LocusID (NCBI) 100616438
Atlas_Id 69545
Location 1p36.22  [Link to chromosome band 1p36]
Location_base_pair Starts at 12191713 and ends at 12191773 bp from pter ( according to hg38-Dec_2013)

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)MIR4632   41593
Cards
Entrez_Gene (NCBI)MIR4632  100616438  microRNA 4632
Aliases
GeneCards (Weizmann)MIR4632
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr1:12191713-12191773 [Contig_View]  MIR4632 [Vega]
TCGA cBioPortalMIR4632
AceView (NCBI)MIR4632
Genatlas (Paris)MIR4632
WikiGenes100616438
SOURCE (Princeton)MIR4632
Genetics Home Reference (NIH)MIR4632
miRBaseMIR4632
dbDEMCMIR4632
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4632  -     chr1:12191713-12191773 +  1p36.22   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4632  -     1p36.22   [Description]    (hg19-Feb_2009)
EnsemblMIR4632 - 1p36.22 [CytoView hg19]  MIR4632 - 1p36.22 [CytoView hg38]
Mapping of homologs : NCBIMIR4632 [Mapview hg19]  MIR4632 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4632
Gene ExpressionMIR4632 [ NCBI-GEO ]   MIR4632 [ EBI - ARRAY_EXPRESS ]   MIR4632 [ SEEK ]   MIR4632 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4632 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616438
GTEX Portal (Tissue expression)MIR4632
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4632
DMDM Disease mutations100616438
Blocks (Seattle)MIR4632
Protein Interaction databases
BioGRIDMIR4632
STRING (EMBL)MIR4632
ZODIACMIR4632
Ontologies - Pathways
Huge Navigator MIR4632 [HugePedia]
snp3D : Map Gene to Disease100616438
BioCentury BCIQMIR4632
ClinGenMIR4632
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616438
Clinical trialMIR4632
Miscellaneous
canSAR (ICR)MIR4632 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4632
EVEXMIR4632
GoPubMedMIR4632
iHOPMIR4632
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 : Fri May 19 11:40:38 CEST 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.