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Category   Symbol Source: HGNC EntrezGene Ensembl GeneCards RNA genes CroW21
GIFtS

MIR132 Gene

RNA gene   GIFtS: 22
GCID: GC17M001953

microRNA 132


(Previous symbol: MIRN132)
 Explore 9 diseases affiliated with
MIR132 via our new
 Human Malady Compendium 
Biological research products
for MIR132
    

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, and/or 10fRNAdb)
About This Section

Subcategory (RNA class): miRNA

Quality score for this RNA gene is 13

Aliases
MicroRNA 1321 2
MIRN1321 2 5
Hsa-Mir-1321
MiRNA1321
Mir-1321

External Ids:    HGNC: 315161   Entrez Gene: 4069212   Ensembl: ENSG000002077247   OMIM: 6100165   
ORGUL members:    fRNAdb10:FR153883      
miRBase: MI0000449    

Export aliases for MIR132 gene to outside databases

Previous GC identifers: GC17M001927 GC17M001930


(According to Entrez Gene, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
About This Section

Entrez Gene summary for MIR132:
microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene
expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed
by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either
protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an
approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer
ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated
into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the
miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq
represents the predicted microRNA stem-loop. (provided by RefSeq, Sep 2009)




(According to GeneLoc and/or HGNC, and/or
Entrez Gene (NCBI build 37),
and/or miRBase,
Genomic Views according to UCSC (hg19) and Ensembl (release 69), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
Regulatory elements:
   Search SABiosciences Regulatory transcription factor binding sites for MIR132
         Other transcription factors

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Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat MIR132


Genomic Location:
Genomic View: UCSC Golden Path with GeneCards custom track

Entrez Gene cytogenetic band: 17p13.3   Ensembl cytogenetic band:  17p13.3   HGNC cytogenetic band: 17p13.3

MIR132 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
MIR132 gene location

GeneLoc information about chromosome 17         GeneLoc Exon Structure

GeneLoc location for GC17M001953:  view genomic region (via miRBase)     (about GC identifiers)

Start:
1,953,202 bp from pter      End:
1,953,302 bp from pter
Size:
101 bases      Orientation:
minus strand

(According to 1UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to 2PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE MOPED and PaxDb, RefSeq according to NCBI, PDB rendering according to OCA and/or Proteopedia, Recombinant Proteins from EMD Millipore, R&D Systems, GenScript, Enzo Life Sciences, OriGene, Novus Biologicals, Sino Biological, ProSpec, and/or Uscn,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Uscn, Ontologies according to Gene Ontology Consortium 01 Mar 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, Abcam, and/or Uscn)
About This Section

UniProtKB: --


(According to InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
About This Section
  --

(According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013,
bound targets from SABiosciences, miRNA Gene Targets from miRTarBase shRNA from OriGene, RNAi from EMD Millipore, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, and Vector BioLabs, Cell Lines from GenScript, LifeMap BioReagents, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene.)
About This Section

miRNA
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miRTarBase genes targeted by MIR132:
SIRT1(MIRT000333), CDKN1A(MIRT000601), ARHGAP32(MIRT003926)

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(Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Reactome, Tocris Bioscience, GeneGo (Thomson Reuters), QIAGEN, and/or UniProtKB, Sets of similar genes according to GeneDecks, Interaction Networks according to SABiosciences, and/or STRING, Interactions according to 1UniProtKB, 2MINT, 3I2D, and/or 4STRING, with links to IntAct and Ensembl, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene).
About This Section



Interactions:

    Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for MIR132

(Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB, with drugs/clinical trials/news search links to CenterWatch)
About This Section
Browse Small Molecules at EMD Millipore
Browse drugs & compounds from Enzo Life Sciences

Browse Tocris compounds for MIR132
Search CenterWatch for drugs/clinical trials and news about MIR132 

(Secondary structures according to fRNAdb,
GenBank/EMBL/DDBJ Accessions according to
Unigene (Build 235 Homo sapiens; Mar 10 2013) or GenBank,
RefSeq according to Entrez Gene,
DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
exon structure from GeneLoc, alternative splicing isoforms according to ASD and/or ECgene,
RNAi Products from EMD Millipore,
siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN,
Tagged/untagged cDNA clones from OriGene, SwitchGear Genomics, GenScript, DNA2.0, Vector BioLabs, Primers from OriGene, SABiosciences, and/or QIAGEN )
About This Section

1 Ensembl transcript including schematic representation, and UCSC links where relevant:
ENST00000384991(miRNA)

miRNA
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GeneLoc Exon Structure


(RNA expression data according to H-InvDB, NONCODE, miRBase, and RNAdb, Expression images according to data from BioGPS, Illumina Human BodyMap, and CGAP SAGE, Sets of similar genes according to GeneDecks, in vivo and in vitro expression data from LifeMap Discovery™, plus additional links to Genevestigator, and/or SOURCE, and/or BioGPS, and/or UniProtKB,
PCR Arrays from SABiosciences, Primers from OriGene, SABiosciences, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
About This Section

Expression evidence for MIR132:none

MIR132 expression in normal human tissues (normalized intensities)
See probesets specificity/sensitivity at GeneAnnot
About this imageBioGPS
CGAP TAG: --

Microarray
RNAseq (Illumina Body Map)
(100×FPKM)½
SAGE (Serial Analysis of Gene Expression)

About this image    SABiosciences Custom PCR Arrays for MIR132
Primer
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In Situ
Assay Products:
 

 
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(Orthologs according to 1,2HomoloGene (2older version, for species not in 1newer version), 3euGenes, 4SGD , 5MGI Mar 06 2013, with possible further links to Flybase and/or WormBase, and/or 6Ensembl pan taxonomic compara , Gene Trees according to Ensembl and TreeFam)
About This Section
  --

ENSEMBL Gene Tree for MIR132 (if available)
TreeFam Gene Tree for MIR132 (if available) 

(Paralogs according to 1HomoloGene,
2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
About This Section
Paralogs for MIR132 gene
MIR2122  

MIR132 for paralogs           About GeneDecksing



(SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, UniProtKB, and DNA2.0, Linkage Disequilibrium by HapMap, Structural Variations(CNVs/InDels/Inversions) from the Database of Genomic Variants, Mutations from the Human Gene Mutation Database (HGMD) and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers from QIAGEN, Cancer Mutation PCR Arrays and Assays and Copy Number PCR Arrays from SABiosciences)
About This Section

10/18 NCBI SNPs in MIR132 are shown (see all 18    About this table
Genomic DataTranscription Related DataAllele Frequencies
SNP IDValidClinical
significance
Chr 17 posSequence#AA
Chg
TypeMore#Allele
freq
PopTotal
sample
More
----------
rs38038071,2
C,H,--1952728(+) GGGGAC/GCCTTC 1 -- ds50014Minor allele frequency- G:0.00NS EA 416
rs1832744471,2
--1952858(+) ACTGTC/TTTCAG 1 -- ds50010--------
rs38038081,2
C,F,--1952977(+) GGCTGG/AGATAC 1 -- ds50012Minor allele frequency- A:0.28NA EA 240
rs29579241,2
C,--1953037(-) GCGCGG/TCCTGC 1 -- ds50018Minor allele frequency- T:0.07NA WA EA 368
rs2016669201,2
--1953831(+) GGCGT-/GGGGGG 2 -- us2k10--------
rs1494433751,2
C,--1953851(+) CCTGG-/CGAGGC 2 -- us2k10--------
rs1174276531,2
F,--1954155(+) CCCAAA/GAAAGC 2 -- us2k11Minor allele frequency- G:0.38EA 120
rs1446170701,2
C,--1954162(+) AAGCC-/GGGGGG 2 -- us2k10--------
rs1865448341,2
--1954522(+) CATGCA/GGCCGC 2 -- us2k10--------
rs1913683641,2
--1954553(+) CTGCCC/GACGTC 2 -- us2k10--------

HapMap Linkage Disequilibrium report for MIR132 (1953202 - 1953302 bp)
Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
Database of Genomic Variants (DGV): 1 variation for MIR132
     1 Indel: 11123

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(in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
About This Section

MIR132 for disorders           About GeneDecksing

OMIM gene information: 610016    OMIM disorders: --

9 diseases for MIR132:    About MalaCards
supranuclear palsy    progressive supranuclear palsy    rheumatoid arthritis    cervical cancer
cervicitis    arthritis    retinoblastoma    pancreatic cancer
pancreatitis

Human Genome Epidemiology (HuGE) Navigator: MIR132 (1 document)

Export disorders for MIR132 gene to outside databases

(in PubMed. Associations of this gene to articles via 1Entrez Gene, 2UniProtKB/Swiss-Prot, 3HGNC, 4GAD, 5PharmGKB, 6HMDB, 7DrugBank, 8UniProtKB/TrEMBL, 9 Novoseek, and/or 10fRNAdb)
About This Section

PubMed articles for MIR132 gene, integrated from 9 sources (see all 17):
(articles sorted by number of sources associating them with MIR132)
    Utopia: connect your pdf to the dynamic
world of online information

  1. MicroRNA-132 dysregulation in schizophrenia has implic ations for both neurodevelopment and adult brain function. (PubMed id 22315408)1 Miller B.H....Wahlestedt C. (2012)
  2. MicroRNA-132 targets HB-EGF upon IgE-mediated activati on in murine and human mast cells. (PubMed id 21853268)1 Molnar V....Falus A. (2012)
  3. MicroRNA regulation of STAT4 protein expression: rapid and sensitive modulation of IL-12 signaling in human natural killer cells. (PubMed id 22077060)1 Huang Y....Dayton A.I. (2011)
  4. MicroRNA-132 loss is associated with tau exon 10 incl usion in progressive supranuclear palsy. (PubMed id 21807765)1 Smith P.Y....HAcbert S.S. (2011)
  5. miR-132 and miR-212 are increased in pancreatic cance r and target the retinoblastoma tumor suppressor. (PubMed id 21329664)1 Park J.K....Schmittgen T.D. (2011)
  6. Downregulation of miR-132 by promoter methylation con tributes to pancreatic cancer development. (PubMed id 21665894)1 Zhang S....Shao C. (2011)
  7. MicroRNA-132-mediated loss of p120RasGAP activates th e endothelium to facilitate pathological angiogenesis. (PubMed id 20676106)1 Anand S....Cheresh D.A. (2010)
  8. miR-132 regulates antiviral innate immunity through s uppression of the p300 transcriptional co-activator. (PubMed id 20418869)1 Lagos D....Boshoff C. (2010)
  9. Novel genetic variants in miR-191 gene and familial o varian cancer. (PubMed id 20167074)1 Shen J....Zhao H. (2010)
  10. MicroRNA 132 regulates nutritional stress-induced che mokine production through repression of SirT1. (PubMed id 19819989)1 Strum J.C....Waters K.M. (2009)

(in PubMed, OMIM, and NCBI Bookshelf)
About This Section
 ANDOR
Aliases
Free Text  

  Query String
PubMed
OMIM
NCBI Bookshelf
  (Note: In FireFox, select the above section and copy using Ctrl-C)

(According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
About This Section
Entrez Gene: 406921 HGNC: 31516 Ensembl:ENSG00000207724 miRBase: hsa-mir-132 euGenes: HUgn406921
ECgene: MIR132 H-InvDB: MIR132

(According to HUGE)
About This Section
  --

(According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL,
Wikipedia and/or GeneReviews via UniProtKB/Swiss-Prot)
About This Section
NameDescription
PharmGKB entry for MIR132 Pharmacogenomics, SNPs, Pathways

(Patent information from GeneIP,
Licensable technologies from WIS Yeda, Salk, Tufts,
IP news from LifeMap Sciences, Inc.)
About This Section
Patent Information for MIR132 gene:
Search GeneIP for patents involving MIR132

GeneCards and IP:
Japan Patent Office Licenses GeneCards     European Patent Office Licenses GeneCards     Improving the IP Search



(Antibodies, recombinant proteins, and assays from EMD Millipore, R&D Systems, OriGene, QIAGEN, GenScript, Cell Signaling Technology, SABiosciences, Novus Biologicals, Sino Biological, Enzo Life Sciences, Abcam, ProSpec, Uscn, Thermo Fisher Scientific, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Cell lines from GenScript and LifeMap BioReagents, PCR Arrays from SABiosciences, Drugs and/or compounds from EMD Millipore, Tocris Bioscience, and/or Enzo Life Sciences),
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