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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Maobtm1Shih
targeted mutation 1, Jean C Shih
MGI:2180752
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Maobtm1Shih/Maobtm1Shih either: (involves: 129S/SvEv) or (involves: 129S4/SvJae) MGI:3042587
cx2
MaoaK284stopMaobtm1Shih/Y either: (involves: 129S/SvEv * 129S6/SvEvTac) or (involves: 129S4/SvJae * 129S6/SvEvTac) MGI:3511894


Genotype
MGI:3042587
hm1
Allelic
Composition
Maobtm1Shih/Maobtm1Shih
Genetic
Background
either: (involves: 129S/SvEv) or (involves: 129S4/SvJae)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Maobtm1Shih mutation (2 available); any Maob mutation (11 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
N
• mutant mice displayed normal working memory in a Y maize test, and exhibited no significant alteration in the open-field test or the elevated plus maize test relative to wild-type
• mutants exhibited significantly increased mobility in the forced swim test, suggesting a state of hyperactivity and increased vigilance to stress
• mutants showed no adaptation to inescapable stress, indicating a sustained stress-induced hyperactivity
• notably, mutants did not display increased locomotion in the open field test

homeostasis/metabolism
N
• mutant mice displayed normal concentrations of 5-HT, 5-hydroxy-3-indole-acetic acid (5-HIAA), dopamine (DA), dihydroxyphenylacetic acid (DOPAC), homovanillic acid (HVA), 3-methoxytyramine (3-MT), norepinephrine (NE) and 3-methoxy-4-hydroxy-phenylglycol (MHPG) in various brain regions relative to wild-type
• MPTP neurotoxicity resulted in the depletion of DA, DOPAC and possibly HVA in wild-type mice; in contrast, mutants suffered no apparent MPTP toxicity of dopaminergic terminals in the striatum
• urinary beta-phenylethylamine (PEA) excretion showed an 8-fold increase in mutant mice relative to wild-type; notably, brain levels of PEA were also increased ~8-fold

renal/urinary system
• urinary beta-phenylethylamine (PEA) excretion showed an 8-fold increase in mutant mice relative to wild-type; notably, brain levels of PEA were also increased ~8-fold

nervous system
• MPTP neurotoxicity resulted in the depletion of DA, DOPAC and possibly HVA in wild-type mice; in contrast, mutants suffered no apparent MPTP toxicity of dopaminergic terminals in the striatum

cellular
• MPTP neurotoxicity resulted in the depletion of DA, DOPAC and possibly HVA in wild-type mice; in contrast, mutants suffered no apparent MPTP toxicity of dopaminergic terminals in the striatum




Genotype
MGI:3511894
cx2
Allelic
Composition
MaoaK284stopMaobtm1Shih/Y
Genetic
Background
either: (involves: 129S/SvEv * 129S6/SvEvTac) or (involves: 129S4/SvJae * 129S6/SvEvTac)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
MaoaK284stop mutation (2 available); any Maoa mutation (10 available)
Maobtm1Shih mutation (2 available); any Maob mutation (11 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• exploratory activity is reduced as is time spent in the center of the field
• in the resident-intruder test mutants display a significant increase in anti-social behavior with a decrease in latency to attack and increased time spent chasing the intruder, as well as a decrease in investigative behavior
• in an elevated Plus-maze, mutants exhibit more freezing or crouching postures, fewer entries into either the open or closed arms, proportionally more entries into the closed arms, and fewer rearing events

homeostasis/metabolism
• dopamine levels are increased 1.7-fold
• brain levels of norepinephrine and phenylethylamine are increased 2.2-, and 15.7-fold, respectively
• brain levels of serotonin are increased 8.5-fold





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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory