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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Minar2tm1b(KOMP)Wtsi
targeted mutation 1b, Wellcome Trust Sanger Institute
MGI:5637144
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Minar2tm1b(KOMP)Wtsi/Minar2tm1b(KOMP)Wtsi C57BL/6N-Minar2tm1b(KOMP)Wtsi/Wtsi MGI:5756630


Genotype
MGI:5756630
hm1
Allelic
Composition
Minar2tm1b(KOMP)Wtsi/Minar2tm1b(KOMP)Wtsi
Genetic
Background
C57BL/6N-Minar2tm1b(KOMP)Wtsi/Wtsi
Cell Lines EPD0770_5_F06
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Minar2tm1b(KOMP)Wtsi mutation (1 available); any Minar2 mutation (18 available)
Data Sources
phenotype observed in females
phenotype observed in males
N normal phenotype
adipose tissue

behavior/neurological
• mice are slower to engage in exploratory behavior in a new environment
• mice show delayed hind-limb reflex
• mice are unable to display hind-limb clasping
• mice take longer to turn and descend the pole than wild-type mice in the pole test, with mice showing difficulty in orienting downwards completely
• mice show more foot slips than wild-type mice in traversing the balance beam
• mice struggle to maintain grip and frequently fail to remain on the bar on a horizontal bar and show reduced grip strength
• mice exhibit abnormal gait, meandering from side to side through the walkway mice have a greater average distance between ipsilateral fore and hind paw prints and greater variation in stride width, indicating that mice walk with more irregular, less uniform step alterations compared to wild-type mice
• mice show less rearing in a new environment; mice attempt to rear by standing in hind limbs but misjudge the distance by standing too far away from the wall or only rest one forelimb on the wall indicating impaired rearing ability
• some mice present with bradykinesia-like symptoms which is more prominent in older mice

growth/size/body

hearing/vestibular/ear

homeostasis/metabolism

nervous system
• loss of TH+ cells in the substantia nigra pars compacta

skeleton

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Parkinson's disease DOID:14330 OMIM:PS168600
J:298983





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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory