Atlas of Genetics and Cytogenetics in Oncology and Haematology


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MIR4422HG (MIR4422 host gene)

Identity

Alias_symbol (synonym)RP11-101C11.1
Other alias-
HGNC (Hugo) MIR4422HG
LocusID (NCBI) 109729135
Atlas_Id 80081
Location 1p32.3  [Link to chromosome band 1p32]
Location_base_pair Starts at 55217861 and ends at 55234177 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)MIR4422HG   53113
Cards
Entrez_Gene (NCBI)MIR4422HG  109729135  MIR4422 host gene
Aliases
GeneCards (Weizmann)MIR4422HG
Ensembl hg19 (Hinxton)ENSG00000231090 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000231090 [Gene_View]  chr1:55217861-55234177 [Contig_View]  MIR4422HG [Vega]
ICGC DataPortalENSG00000231090
TCGA cBioPortalMIR4422HG
AceView (NCBI)MIR4422HG
Genatlas (Paris)MIR4422HG
WikiGenes109729135
SOURCE (Princeton)MIR4422HG
Genetics Home Reference (NIH)MIR4422HG
miRBaseMIR4422HG
dbDEMCMIR4422HG
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4422HG  -     chr1:55217861-55234177 +  1p32.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4422HG  -     1p32.3   [Description]    (hg19-Feb_2009)
EnsemblMIR4422HG - 1p32.3 [CytoView hg19]  MIR4422HG - 1p32.3 [CytoView hg38]
Mapping of homologs : NCBIMIR4422HG [Mapview hg19]  MIR4422HG [Mapview hg38]
Gene and transcription
Genbank (Entrez)AW083067 BX112869
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4422HG
Cluster EST : UnigeneHs.738147 [ NCBI ]
CGAP (NCI)Hs.738147
Alternative Splicing GalleryENSG00000231090
Gene ExpressionMIR4422HG [ NCBI-GEO ]   MIR4422HG [ EBI - ARRAY_EXPRESS ]   MIR4422HG [ SEEK ]   MIR4422HG [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4422HG [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)109729135
GTEX Portal (Tissue expression)MIR4422HG
Human Protein AtlasENSG00000231090-MIR4422HG [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4422HG
DMDM Disease mutations109729135
Blocks (Seattle)MIR4422HG
Human Protein Atlas [tissue]ENSG00000231090-MIR4422HG [tissue]
Protein Interaction databases
FunCoupENSG00000231090
BioGRIDMIR4422HG
STRING (EMBL)MIR4422HG
ZODIACMIR4422HG
Ontologies - Pathways
Huge Navigator MIR4422HG [HugePedia]
snp3D : Map Gene to Disease109729135
BioCentury BCIQMIR4422HG
ClinGenMIR4422HG
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD109729135
Clinical trialMIR4422HG
Miscellaneous
canSAR (ICR)MIR4422HG (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4422HG
EVEXMIR4422HG
GoPubMedMIR4422HG
iHOPMIR4422HG
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 13:01:36 CET 2017

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