Atlas of Genetics and Cytogenetics in Oncology and Haematology


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MIR4771-1 (microRNA 4771-1)

Identity

Alias_symbol (synonym)hsa-mir-4771-1
Other alias-
HGNC (Hugo) MIR4771-1
LocusID (NCBI) 100616370
Atlas_Id 77653
Location 2p11.2  [Link to chromosome band 2p11]
Location_base_pair Starts at 87421909 and ends at 87421982 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


External links

Nomenclature
HGNC (Hugo)MIR4771-1   41901
Cards
Entrez_Gene (NCBI)MIR4771-1  100616370  microRNA 4771-1
Aliases
GeneCards (Weizmann)MIR4771-1
Ensembl hg19 (Hinxton)ENSG00000264793 [Gene_View]  chr2:87421909-87421982 [Contig_View]  MIR4771-1 [Vega]
Ensembl hg38 (Hinxton)ENSG00000264793 [Gene_View]  chr2:87421909-87421982 [Contig_View]  MIR4771-1 [Vega]
ICGC DataPortalENSG00000264793
TCGA cBioPortalMIR4771-1
AceView (NCBI)MIR4771-1
Genatlas (Paris)MIR4771-1
WikiGenes100616370
SOURCE (Princeton)MIR4771-1
Genetics Home Reference (NIH)MIR4771-1
miRBaseMIR4771-1
dbDEMCMIR4771-1
Genomic and cartography
GoldenPath hg19 (UCSC)MIR4771-1  -     chr2:87421909-87421982 +  2p11.2   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIR4771-1  -     2p11.2   [Description]    (hg38-Dec_2013)
EnsemblMIR4771-1 - 2p11.2 [CytoView hg19]  MIR4771-1 - 2p11.2 [CytoView hg38]
Mapping of homologs : NCBIMIR4771-1 [Mapview hg19]  MIR4771-1 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000002 NC_018913 NT_022184 NW_004929300
Consensus coding sequences : CCDS (NCBI)MIR4771-1
Alternative Splicing GalleryENSG00000264793
Gene ExpressionMIR4771-1 [ NCBI-GEO ]   MIR4771-1 [ EBI - ARRAY_EXPRESS ]   MIR4771-1 [ SEEK ]   MIR4771-1 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4771-1 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616370
GTEX Portal (Tissue expression)MIR4771-1
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4771-1
DMDM Disease mutations100616370
Blocks (Seattle)MIR4771-1
Human Protein AtlasENSG00000264793
Protein Interaction databases
FunCoupENSG00000264793
BioGRIDMIR4771-1
STRING (EMBL)MIR4771-1
ZODIACMIR4771-1
Ontologies - Pathways
Huge Navigator MIR4771-1 [HugePedia]
snp3D : Map Gene to Disease100616370
BioCentury BCIQMIR4771-1
ClinGenMIR4771-1
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616370
Clinical trialMIR4771-1
Miscellaneous
canSAR (ICR)MIR4771-1 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4771-1
EVEXMIR4771-1
GoPubMedMIR4771-1
iHOPMIR4771-1
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Mar 14 12:31:02 CET 2017

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