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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Fmc1em1Aitn
endonuclease-mediated mutation 1, Ayako Isotani
MGI:6392175
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Fmc1em1Aitn/Fmc1em1Aitn C57BL/6JJmsSlc-Fmc1em1Aitn MGI:6392233
ht2
Fmc1em1Aitn/Fmc1+ C57BL/6JJmsSlc-Fmc1em1Aitn MGI:6392234


Genotype
MGI:6392233
hm1
Allelic
Composition
Fmc1em1Aitn/Fmc1em1Aitn
Genetic
Background
C57BL/6JJmsSlc-Fmc1em1Aitn
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fmc1em1Aitn mutation (0 available); any Fmc1 mutation (19 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice begin to die after birth through 14 days of age
• mice begin to die after birth through 14 days of age

cellular
• reduced complex I activity in the heart
• however, complex I activity in the brain is normal




Genotype
MGI:6392234
ht2
Allelic
Composition
Fmc1em1Aitn/Fmc1+
Genetic
Background
C57BL/6JJmsSlc-Fmc1em1Aitn
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fmc1em1Aitn mutation (0 available); any Fmc1 mutation (19 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• mice are protected from MPTP-induced motor deficits and dopaminergic neurons in the substantia nigra compared with wild-type mice
• MPTP-treated mice fail to exhibit a decrease in complex I activity unlike wild-type mice

nervous system
• mice are protected from MPTP-induced motor deficits and dopaminergic neurons in the substantia nigra compared with wild-type mice

behavior/neurological
• mice are protected from MPTP-induced motor deficits

homeostasis/metabolism
• mice are protected from MPTP-induced motor deficits and dopaminergic neurons in the substantia nigra compared with wild-type mice





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory