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

MIR4698 (microRNA 4698)

Identity

Alias_symbol (synonym)hsa-mir-4698
Other alias-
HGNC (Hugo) MIR4698
LocusID (NCBI) 100616486
Atlas_Id 69614
Location 12q13.11  [Link to chromosome band 12q13]
Location_base_pair Starts at 47187812 and ends at 47187891 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)MIR4698   41867
Cards
Entrez_Gene (NCBI)MIR4698  100616486  microRNA 4698
Aliases
GeneCards (Weizmann)MIR4698
Ensembl hg19 (Hinxton)ENSG00000263838 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000263838 [Gene_View]  chr12:47187812-47187891 [Contig_View]  MIR4698 [Vega]
ICGC DataPortalENSG00000263838
TCGA cBioPortalMIR4698
AceView (NCBI)MIR4698
Genatlas (Paris)MIR4698
WikiGenes100616486
SOURCE (Princeton)MIR4698
Genetics Home Reference (NIH)MIR4698
miRBaseMIR4698
dbDEMCMIR4698
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4698  -     chr12:47187812-47187891 +  12q13.11   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4698  -     12q13.11   [Description]    (hg19-Feb_2009)
EnsemblMIR4698 - 12q13.11 [CytoView hg19]  MIR4698 - 12q13.11 [CytoView hg38]
Mapping of homologs : NCBIMIR4698 [Mapview hg19]  MIR4698 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4698
Alternative Splicing GalleryENSG00000263838
Gene ExpressionMIR4698 [ NCBI-GEO ]   MIR4698 [ EBI - ARRAY_EXPRESS ]   MIR4698 [ SEEK ]   MIR4698 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4698 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616486
GTEX Portal (Tissue expression)MIR4698
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4698
DMDM Disease mutations100616486
Blocks (Seattle)MIR4698
Human Protein AtlasENSG00000263838
Protein Interaction databases
FunCoupENSG00000263838
BioGRIDMIR4698
STRING (EMBL)MIR4698
ZODIACMIR4698
Ontologies - Pathways
Huge Navigator MIR4698 [HugePedia]
snp3D : Map Gene to Disease100616486
BioCentury BCIQMIR4698
ClinGenMIR4698
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616486
Clinical trialMIR4698
Miscellaneous
canSAR (ICR)MIR4698 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4698
EVEXMIR4698
GoPubMedMIR4698
iHOPMIR4698
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 11:40:52 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.