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MIR4322 (microRNA 4322)

Identity

Alias_symbol (synonym)hsa-mir-4322
Other alias-
HGNC (Hugo) MIR4322
LocusID (NCBI) 100422925
Atlas_Id 69429
Location 19p13.2  [Link to chromosome band 19p13]
Location_base_pair Starts at 10230413 and ends at 10230485 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)

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)MIR4322   38261
Cards
Entrez_Gene (NCBI)MIR4322  100422925  microRNA 4322
Aliases
GeneCards (Weizmann)MIR4322
Ensembl hg19 (Hinxton)ENSG00000264266 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000264266 [Gene_View]  chr19:10230413-10230485 [Contig_View]  MIR4322 [Vega]
ICGC DataPortalENSG00000264266
TCGA cBioPortalMIR4322
AceView (NCBI)MIR4322
Genatlas (Paris)MIR4322
WikiGenes100422925
SOURCE (Princeton)MIR4322
Genetics Home Reference (NIH)MIR4322
miRBaseMIR4322
dbDEMCMIR4322
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4322  -     chr19:10230413-10230485 +  19p13.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4322  -     19p13.2   [Description]    (hg19-Feb_2009)
EnsemblMIR4322 - 19p13.2 [CytoView hg19]  MIR4322 - 19p13.2 [CytoView hg38]
Mapping of homologs : NCBIMIR4322 [Mapview hg19]  MIR4322 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4322
Alternative Splicing GalleryENSG00000264266
Gene ExpressionMIR4322 [ NCBI-GEO ]   MIR4322 [ EBI - ARRAY_EXPRESS ]   MIR4322 [ SEEK ]   MIR4322 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4322 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100422925
GTEX Portal (Tissue expression)MIR4322
Human Protein AtlasENSG00000264266-MIR4322 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4322
DMDM Disease mutations100422925
Blocks (Seattle)MIR4322
Human Protein Atlas [tissue]ENSG00000264266-MIR4322 [tissue]
Protein Interaction databases
FunCoupENSG00000264266
BioGRIDMIR4322
STRING (EMBL)MIR4322
ZODIACMIR4322
Ontologies - Pathways
Huge Navigator MIR4322 [HugePedia]
snp3D : Map Gene to Disease100422925
BioCentury BCIQMIR4322
ClinGenMIR4322
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100422925
Chemical/Pharm GKB GenePA165393805
Clinical trialMIR4322
Miscellaneous
canSAR (ICR)MIR4322 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4322
EVEXMIR4322
GoPubMedMIR4322
iHOPMIR4322
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Tue Nov 21 13:39:07 CET 2017

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