Atlas of Genetics and Cytogenetics in Oncology and Haematology


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MIR3622B (microRNA 3622b)

Identity

Alias_symbol (synonym)hsa-mir-3622b
Other alias-
HGNC (Hugo) MIR3622B
LocusID (NCBI) 100500871
Atlas_Id 69255
Location 8p21.1  [Link to chromosome band 8p21]
Location_base_pair Starts at 27701673 and ends at 27701767 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)MIR3622B   38961
Cards
Entrez_Gene (NCBI)MIR3622B  100500871  microRNA 3622b
Aliases
GeneCards (Weizmann)MIR3622B
Ensembl hg19 (Hinxton)ENSG00000265075 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000265075 [Gene_View]  chr8:27701673-27701767 [Contig_View]  MIR3622B [Vega]
ICGC DataPortalENSG00000265075
TCGA cBioPortalMIR3622B
AceView (NCBI)MIR3622B
Genatlas (Paris)MIR3622B
WikiGenes100500871
SOURCE (Princeton)MIR3622B
Genetics Home Reference (NIH)MIR3622B
miRBaseMIR3622B
dbDEMCMIR3622B
Genomic and cartography
GoldenPath hg38 (UCSC)MIR3622B  -     chr8:27701673-27701767 -  8p21.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR3622B  -     8p21.1   [Description]    (hg19-Feb_2009)
EnsemblMIR3622B - 8p21.1 [CytoView hg19]  MIR3622B - 8p21.1 [CytoView hg38]
Mapping of homologs : NCBIMIR3622B [Mapview hg19]  MIR3622B [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR3622B
Alternative Splicing GalleryENSG00000265075
Gene ExpressionMIR3622B [ NCBI-GEO ]   MIR3622B [ EBI - ARRAY_EXPRESS ]   MIR3622B [ SEEK ]   MIR3622B [ MEM ]
Gene Expression Viewer (FireBrowse)MIR3622B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100500871
GTEX Portal (Tissue expression)MIR3622B
Human Protein AtlasENSG00000265075-MIR3622B [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR3622B
DMDM Disease mutations100500871
Blocks (Seattle)MIR3622B
Human Protein Atlas [tissue]ENSG00000265075-MIR3622B [tissue]
Protein Interaction databases
FunCoupENSG00000265075
BioGRIDMIR3622B
STRING (EMBL)MIR3622B
ZODIACMIR3622B
Ontologies - Pathways
Huge Navigator MIR3622B [HugePedia]
snp3D : Map Gene to Disease100500871
BioCentury BCIQMIR3622B
ClinGenMIR3622B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100500871
Clinical trialMIR3622B
Miscellaneous
canSAR (ICR)MIR3622B (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR3622B
EVEXMIR3622B
GoPubMedMIR3622B
iHOPMIR3622B
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 13:18:33 CET 2017

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