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

MIR4757 (microRNA 4757)

Identity

Alias_symbol (synonym)hsa-mir-4757
Other alias-
HGNC (Hugo) MIR4757
LocusID (NCBI) 100616307
Atlas_Id 69670
Location 2p24.1  [Link to chromosome band 2p24]
Location_base_pair Starts at 19348429 and ends at 19348505 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)MIR4757   41746
Cards
Entrez_Gene (NCBI)MIR4757  100616307  microRNA 4757
Aliases
GeneCards (Weizmann)MIR4757
Ensembl hg19 (Hinxton)ENSG00000266738 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000266738 [Gene_View]  chr2:19348429-19348505 [Contig_View]  MIR4757 [Vega]
ICGC DataPortalENSG00000266738
TCGA cBioPortalMIR4757
AceView (NCBI)MIR4757
Genatlas (Paris)MIR4757
WikiGenes100616307
SOURCE (Princeton)MIR4757
Genetics Home Reference (NIH)MIR4757
miRBaseMIR4757
dbDEMCMIR4757
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4757  -     chr2:19348429-19348505 +  2p24.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4757  -     2p24.1   [Description]    (hg19-Feb_2009)
EnsemblMIR4757 - 2p24.1 [CytoView hg19]  MIR4757 - 2p24.1 [CytoView hg38]
Mapping of homologs : NCBIMIR4757 [Mapview hg19]  MIR4757 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4757
Alternative Splicing GalleryENSG00000266738
Gene ExpressionMIR4757 [ NCBI-GEO ]   MIR4757 [ EBI - ARRAY_EXPRESS ]   MIR4757 [ SEEK ]   MIR4757 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4757 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616307
GTEX Portal (Tissue expression)MIR4757
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4757
DMDM Disease mutations100616307
Blocks (Seattle)MIR4757
Human Protein AtlasENSG00000266738
Protein Interaction databases
FunCoupENSG00000266738
BioGRIDMIR4757
STRING (EMBL)MIR4757
ZODIACMIR4757
Ontologies - Pathways
Huge Navigator MIR4757 [HugePedia]
snp3D : Map Gene to Disease100616307
BioCentury BCIQMIR4757
ClinGenMIR4757
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616307
Clinical trialMIR4757
Miscellaneous
canSAR (ICR)MIR4757 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4757
EVEXMIR4757
GoPubMedMIR4757
iHOPMIR4757
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 13:29:18 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.