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Mir132 Gene Detail
Summary
  • Symbol
    Mir132
  • Name
    microRNA 132
  • Synonyms
    Mirn132, mmu-mir-132
Location &
Maps
more
  • Sequence Map
    Chr11:75064508-75064573 bp, + strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 11, 45.76 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    60 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_2676817
miRNA gene Chr11:75064508-75064573 (+)
129S1/SvImJ MGP_129S1SvImJ_G0007840
miRNA gene Chr11:75905293-75905358 (+)
A/J MGP_AJ_G0007835
miRNA gene Chr11:73086238-73086303 (+)
AKR/J MGP_AKRJ_G0007810
miRNA gene Chr11:75301138-75301203 (+)
BALB/cJ MGP_BALBcJ_G0007813
miRNA gene Chr11:73456925-73456990 (+)
C3H/HeJ MGP_C3HHeJ_G0007760
miRNA gene Chr11:75314250-75314315 (+)
C57BL/6NJ MGP_C57BL6NJ_G0007991
miRNA gene Chr11:78280137-78280202 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0007135
miRNA gene Chr11:70102758-70102823 (+)
CAST/EiJ MGP_CASTEiJ_G0007653
miRNA gene Chr11:75702550-75702615 (+)
CBA/J MGP_CBAJ_G0007731
miRNA gene Chr11:81717314-81717379 (+)
DBA/2J MGP_DBA2J_G0007766
miRNA gene Chr11:72692210-72692275 (+)
FVB/NJ MGP_FVBNJ_G0007784
miRNA gene Chr11:72253520-72253585 (+)
LP/J MGP_LPJ_G0007844
miRNA gene Chr11:76498094-76498159 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0007754
miRNA gene Chr11:82303576-82303641 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0007988
miRNA gene Chr11:75486824-75486889 (+)
PWK/PhJ MGP_PWKPhJ_G0007581
miRNA gene Chr11:73388533-73388598 (+)
SPRET/EiJ MGP_SPRETEiJ_G0007476
miRNA gene Chr11:75057896-75057961 (+)
WSB/EiJ MGP_WSBEiJ_G0007721
miRNA gene Chr11:75305808-75305873 (+)



Homology
more
  • Human Ortholog
    MIR132, microRNA 132
  • Vertebrate Orthologs
    2
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    MIR132, microRNA 132
  • Synonyms
    mir-132, MIRN132, miRNA132
  • Links
    NCBI Gene ID: 406921

  • Chr Location
    chr17:2049908-2050008 (-)  GRCh38

Human Diseases
more
  • Diseases
    1 with human MIR132 associations

Human Disease Mouse Models
      
IDs
Click on a disease name to see all genes associated with that disease.

Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    9 phenotype references
Mice homozygous for an allele lacking both Mir212 and Mir132 exhibit disrupted cortical synaptic transmission and plasticity. Mice homozygous for another knock-out allele exhibit abnormal mammary gland development (see Mirc19).
Gene Ontology
(GO)
Classifications
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  • All GO Annotations
  • GO References
Molecular Function

carbohydrate derivative binding
cytoskeletal protein binding
DNA binding
enzyme regulator
hydrolase
ligase
lipid binding
oxidoreductase
RNA binding
signaling receptor activity
signaling receptor binding
transcription
transferase
transporter
Biological Process

carbohydrate derivative metabolism
cell differentiation
cell population proliferation
cellular component organization
DNA-templated transcription
establishment of localization
homeostatic process
immune system process
lipid metabolic process
programmed cell death
protein metabolic process
response to stimulus
signaling
system development
Cellular Component

cell projection
cytoplasmic vesicle
cytoskeleton
cytosol
endoplasmic reticulum
endosome
extracellular region
Golgi apparatus
mitochondrion
membraneless organelle
nucleus
organelle envelope
organelle lumen
plasma membrane
protein-containing complex
synapse
vacuole
Click cells to view annotations.
Expression
less
Expression Overview

early conceptus
embryo ectoderm
embryo endoderm
embryo mesoderm
embryo mesenchyme
extraembryonic component
alimentary system
auditory system
branchial arches
cardiovascular system
connective tissue
endocrine system
exocrine system
hemolymphoid system
integumental system
limbs
liver and biliary system
musculoskeletal system
nervous system
olfactory system
reproductive system
respiratory system
urinary system
visual system
Click cells to view annotations.


  • Assay Results
  • Tissues
  • Literature Summary
Sequences &
Gene Models
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  • All Sequences
  • RefSeq
Representative SequencesLengthStrain/SpeciesFlank
genomic 387150 NCBI Gene Model | MGI Sequence Detail 66 C57BL/6J ±  kb
transcript NR_029546 RefSeq | MGI Sequence Detail 66 C57BL/6  
For the selected sequence
Molecular
Reagents
less
  • All nucleic 4
    Primer pair 2
    Other 2
Other Database
Links
less
miRBase MI0000158
References
more
  • Summaries
    All 86
    Developmental Gene Expression 10
    Gene Ontology 6
    Phenotypes 9
  • Earliest
    J:137335 Roderick TH, Chromosomal inversions in studies of mammalian mutagenesis. Genetics. 1979 May;92(1 Pt 1 Suppl):s121-6
  • Latest
    J:344338 Subramanian M, et al., Growth-suppressor microRNAs mediate synaptic overgrowth and behavioral deficits in Fragile X mental retardation protein deficiency. iScience. 2024 Jan 19;27(1):108676

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory