Atlas of Genetics and Cytogenetics in Oncology and Haematology


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MIR4422 (microRNA 4422)

Identity

Alias_symbol (synonym)hsa-mir-4422
Other aliasmir-4422
HGNC (Hugo) MIR4422
LocusID (NCBI) 100616272
Atlas_Id 69440
Location 1p32.3  [Link to chromosome band 1p32]
Location_base_pair Starts at 55691314 and ends at 55691396 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)MIR4422   41654
Cards
Entrez_Gene (NCBI)MIR4422  100616272  microRNA 4422
Aliasesmir-4422
GeneCards (Weizmann)MIR4422
Ensembl hg19 (Hinxton)ENSG00000265822 [Gene_View]  chr1:55691314-55691396 [Contig_View]  MIR4422 [Vega]
Ensembl hg38 (Hinxton)ENSG00000265822 [Gene_View]  chr1:55691314-55691396 [Contig_View]  MIR4422 [Vega]
ICGC DataPortalENSG00000265822
TCGA cBioPortalMIR4422
AceView (NCBI)MIR4422
Genatlas (Paris)MIR4422
WikiGenes100616272
SOURCE (Princeton)MIR4422
Genetics Home Reference (NIH)MIR4422
miRBaseMIR4422
dbDEMCMIR4422
Genomic and cartography
GoldenPath hg19 (UCSC)MIR4422  -     chr1:55691314-55691396 +  1p32.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIR4422  -     1p32.3   [Description]    (hg38-Dec_2013)
EnsemblMIR4422 - 1p32.3 [CytoView hg19]  MIR4422 - 1p32.3 [CytoView hg38]
Mapping of homologs : NCBIMIR4422 [Mapview hg19]  MIR4422 [Mapview hg38]
Gene and transcription
Genbank (Entrez)LM611283
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000001 NC_018912 NT_032977 NW_004929290
Consensus coding sequences : CCDS (NCBI)MIR4422
Alternative Splicing GalleryENSG00000265822
Gene ExpressionMIR4422 [ NCBI-GEO ]   MIR4422 [ EBI - ARRAY_EXPRESS ]   MIR4422 [ SEEK ]   MIR4422 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4422 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616272
GTEX Portal (Tissue expression)MIR4422
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4422
DMDM Disease mutations100616272
Blocks (Seattle)MIR4422
Human Protein AtlasENSG00000265822
Protein Interaction databases
FunCoupENSG00000265822
BioGRIDMIR4422
STRING (EMBL)MIR4422
ZODIACMIR4422
Ontologies - Pathways
Huge Navigator MIR4422 [HugePedia]
snp3D : Map Gene to Disease100616272
BioCentury BCIQMIR4422
ClinGenMIR4422
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616272
Clinical trialMIR4422
Miscellaneous
canSAR (ICR)MIR4422 (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4422
EVEXMIR4422
GoPubMedMIR4422
iHOPMIR4422
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 12:30:03 CET 2017

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