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

MIR4787 (microRNA 4787)

Identity

Alias_symbol (synonym)hsa-mir-4787
Other aliasmir-4787
HGNC (Hugo) MIR4787
LocusID (NCBI) 100616138
Atlas_Id 69701
Location 3p21.2  [Link to chromosome band 3p21]
Location_base_pair Starts at 50675080 and ends at 50675163 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)MIR4787   41653
Cards
Entrez_Gene (NCBI)MIR4787  100616138  microRNA 4787
Aliasesmir-4787
GeneCards (Weizmann)MIR4787
Ensembl hg19 (Hinxton)ENSG00000272543 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000272543 [Gene_View]  chr3:50675080-50675163 [Contig_View]  MIR4787 [Vega]
ICGC DataPortalENSG00000272543
TCGA cBioPortalMIR4787
AceView (NCBI)MIR4787
Genatlas (Paris)MIR4787
WikiGenes100616138
SOURCE (Princeton)MIR4787
Genetics Home Reference (NIH)MIR4787
miRBaseMIR4787
dbDEMCMIR4787
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4787  -     chr3:50675080-50675163 +  3p21.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4787  -     3p21.2   [Description]    (hg19-Feb_2009)
EnsemblMIR4787 - 3p21.2 [CytoView hg19]  MIR4787 - 3p21.2 [CytoView hg38]
Mapping of homologs : NCBIMIR4787 [Mapview hg19]  MIR4787 [Mapview hg38]
Gene and transcription
Genbank (Entrez)LM611422
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4787
Alternative Splicing GalleryENSG00000272543
Gene ExpressionMIR4787 [ NCBI-GEO ]   MIR4787 [ EBI - ARRAY_EXPRESS ]   MIR4787 [ SEEK ]   MIR4787 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4787 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616138
GTEX Portal (Tissue expression)MIR4787
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4787
DMDM Disease mutations100616138
Blocks (Seattle)MIR4787
Human Protein AtlasENSG00000272543
Protein Interaction databases
FunCoupENSG00000272543
BioGRIDMIR4787
STRING (EMBL)MIR4787
ZODIACMIR4787
Ontologies - Pathways
Huge Navigator MIR4787 [HugePedia]
snp3D : Map Gene to Disease100616138
BioCentury BCIQMIR4787
ClinGenMIR4787
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616138
Clinical trialMIR4787
Miscellaneous
canSAR (ICR)MIR4787 (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4787
EVEXMIR4787
GoPubMedMIR4787
iHOPMIR4787
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 : Mon Sep 18 13:29:22 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.