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

MIR4768 (microRNA 4768)

Identity

Alias_symbol (synonym)hsa-mir-4768
Other alias-
HGNC (Hugo) MIR4768
LocusID (NCBI) 100616249
Atlas_Id 69681
Location Xp22.13  [Link to chromosome band Xp22]
Location_base_pair Starts at 17425881 and ends at 17425954 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)MIR4768   41592
Cards
Entrez_Gene (NCBI)MIR4768  100616249  microRNA 4768
Aliases
GeneCards (Weizmann)MIR4768
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chrX:17425881-17425954 [Contig_View]  MIR4768 [Vega]
TCGA cBioPortalMIR4768
AceView (NCBI)MIR4768
Genatlas (Paris)MIR4768
WikiGenes100616249
SOURCE (Princeton)MIR4768
Genetics Home Reference (NIH)MIR4768
miRBaseMIR4768
dbDEMCMIR4768
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4768  -     chrX:17425881-17425954 +  Xp22.13   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4768  -     Xp22.13   [Description]    (hg19-Feb_2009)
EnsemblMIR4768 - Xp22.13 [CytoView hg19]  MIR4768 - Xp22.13 [CytoView hg38]
Mapping of homologs : NCBIMIR4768 [Mapview hg19]  MIR4768 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4768
Gene ExpressionMIR4768 [ NCBI-GEO ]   MIR4768 [ EBI - ARRAY_EXPRESS ]   MIR4768 [ SEEK ]   MIR4768 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4768 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616249
GTEX Portal (Tissue expression)MIR4768
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4768
DMDM Disease mutations100616249
Blocks (Seattle)MIR4768
Protein Interaction databases
BioGRIDMIR4768
STRING (EMBL)MIR4768
ZODIACMIR4768
Ontologies - Pathways
Huge Navigator MIR4768 [HugePedia]
snp3D : Map Gene to Disease100616249
BioCentury BCIQMIR4768
ClinGenMIR4768
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616249
Clinical trialMIR4768
Miscellaneous
canSAR (ICR)MIR4768 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4768
EVEXMIR4768
GoPubMedMIR4768
iHOPMIR4768
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 : Wed May 31 15:28:49 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.