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

MIR4708 (microRNA 4708)

Identity

Alias_symbol (synonym)hsa-mir-4708
Other aliasmir-4708
HGNC (Hugo) MIR4708
LocusID (NCBI) 100616176
Atlas_Id 69622
Location 14q23.3  [Link to chromosome band 14q23]
Location_base_pair Starts at 65801836 and ends at 65801901 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)MIR4708   41824
Cards
Entrez_Gene (NCBI)MIR4708  100616176  microRNA 4708
Aliasesmir-4708
GeneCards (Weizmann)MIR4708
Ensembl hg19 (Hinxton)ENSG00000266740 [Gene_View]  chr14:65801836-65801901 [Contig_View]  MIR4708 [Vega]
Ensembl hg38 (Hinxton)ENSG00000266740 [Gene_View]  chr14:65801836-65801901 [Contig_View]  MIR4708 [Vega]
ICGC DataPortalENSG00000266740
TCGA cBioPortalMIR4708
AceView (NCBI)MIR4708
Genatlas (Paris)MIR4708
WikiGenes100616176
SOURCE (Princeton)MIR4708
Genetics Home Reference (NIH)MIR4708
miRBaseMIR4708
dbDEMCMIR4708
Genomic and cartography
GoldenPath hg19 (UCSC)MIR4708  -     chr14:65801836-65801901 -  14q23.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIR4708  -     14q23.3   [Description]    (hg38-Dec_2013)
EnsemblMIR4708 - 14q23.3 [CytoView hg19]  MIR4708 - 14q23.3 [CytoView hg38]
Mapping of homologs : NCBIMIR4708 [Mapview hg19]  MIR4708 [Mapview hg38]
Gene and transcription
Genbank (Entrez)LM611388
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000014 NC_018925 NT_026437 NW_004929393
Consensus coding sequences : CCDS (NCBI)MIR4708
Alternative Splicing GalleryENSG00000266740
Gene ExpressionMIR4708 [ NCBI-GEO ]   MIR4708 [ EBI - ARRAY_EXPRESS ]   MIR4708 [ SEEK ]   MIR4708 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4708 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616176
GTEX Portal (Tissue expression)MIR4708
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4708
DMDM Disease mutations100616176
Blocks (Seattle)MIR4708
Human Protein AtlasENSG00000266740
Protein Interaction databases
FunCoupENSG00000266740
BioGRIDMIR4708
STRING (EMBL)MIR4708
ZODIACMIR4708
Ontologies - Pathways
Huge Navigator MIR4708 [HugePedia]
snp3D : Map Gene to Disease100616176
BioCentury BCIQMIR4708
ClinGenMIR4708
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616176
Clinical trialMIR4708
Miscellaneous
canSAR (ICR)MIR4708 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4708
EVEXMIR4708
GoPubMedMIR4708
iHOPMIR4708
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 12:30:49 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.