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MIR4448 (microRNA 4448)

Identity

Alias_symbol (synonym)hsa-mir-4448
Other alias-
HGNC (Hugo) MIR4448
LocusID (NCBI) 100616127
Atlas_Id 79843
Location 3q27.1  [Link to chromosome band 3q27]
Location_base_pair Starts at 183886800 and ends at 183886885 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)MIR4448   41604
Cards
Entrez_Gene (NCBI)MIR4448  100616127  microRNA 4448
Aliases
GeneCards (Weizmann)MIR4448
Ensembl hg19 (Hinxton)ENSG00000263932 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000263932 [Gene_View]  ENSG00000263932 [Sequence]  chr3:183886800-183886885 [Contig_View]  MIR4448 [Vega]
ICGC DataPortalENSG00000263932
TCGA cBioPortalMIR4448
AceView (NCBI)MIR4448
Genatlas (Paris)MIR4448
WikiGenes100616127
SOURCE (Princeton)MIR4448
Genetics Home Reference (NIH)MIR4448
miRBaseMIR4448
dbDEMCMIR4448
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4448  -     chr3:183886800-183886885 +  3q27.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4448  -     3q27.1   [Description]    (hg19-Feb_2009)
EnsemblMIR4448 - 3q27.1 [CytoView hg19]  MIR4448 - 3q27.1 [CytoView hg38]
Mapping of homologs : NCBIMIR4448 [Mapview hg19]  MIR4448 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4448
Alternative Splicing GalleryENSG00000263932
Gene ExpressionMIR4448 [ NCBI-GEO ]   MIR4448 [ EBI - ARRAY_EXPRESS ]   MIR4448 [ SEEK ]   MIR4448 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4448 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616127
GTEX Portal (Tissue expression)MIR4448
Human Protein AtlasENSG00000263932-MIR4448 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4448
DMDM Disease mutations100616127
Blocks (Seattle)MIR4448
Human Protein Atlas [tissue]ENSG00000263932-MIR4448 [tissue]
Protein Interaction databases
FunCoupENSG00000263932
BioGRIDMIR4448
STRING (EMBL)MIR4448
ZODIACMIR4448
Ontologies - Pathways
Huge Navigator MIR4448 [HugePedia]
snp3D : Map Gene to Disease100616127
BioCentury BCIQMIR4448
ClinGenMIR4448
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616127
Clinical trialMIR4448
Miscellaneous
canSAR (ICR)MIR4448 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4448
EVEXMIR4448
GoPubMedMIR4448
iHOPMIR4448
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 : Mon Jul 30 14:14:42 CEST 2018

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