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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Mapttm2.1(FUS)Neas
targeted mutation 2.1, Neil A Shneider
MGI:5776230
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
ht1
Mapttm2.1(FUS)Neas/Mapt+ B6J.129P2(129S)-Mapttm2.1(FUS)Neas MGI:5823847


Genotype
MGI:5823847
ht1
Allelic
Composition
Mapttm2.1(FUS)Neas/Mapt+
Genetic
Background
B6J.129P2(129S)-Mapttm2.1(FUS)Neas
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mapttm2.1(FUS)Neas mutation (0 available); any Mapt mutation (428 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• motor neuron degeneration is associated with astrocytosis and microgliosis
• motor neuron degeneration is associated with astrocytosis and microgliosis
• by P40, before motor neuron loss, a significant number of neuromuscular junctions in the tibialis anterior has no associated input, indicating early retraction of motor axons
• loss of motor neurons at lumber level 5 (L5) is first seen at P60 and progresses steadily to P360
• however, no loss of parvalbumin-positive, proprioceptive sensory neurons in the L5 dorsal root ganglia is seen or of motor neuron loss in oculomotor nucleus at P360
• by P40, denervation of the tibialis anterior neuromuscular junctions are seen before motor neuron loss
• denervation of the gastrocnemius muscle is seen at P90 when about 10% of neuromuscular junctions are vacant
• denervation in both the tibialis anterior and gastrocnemius muscles progresses steadily so that by P360, 30.2% and 13.9% of endplates are vacant in the respective muscles
• however, no denervation of the slow sloeus muscle is seen at 1 year

hematopoietic system
• motor neuron degeneration is associated with astrocytosis and microgliosis

immune system
• motor neuron degeneration is associated with astrocytosis and microgliosis





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last database update
05/07/2024
MGI 6.23
The Jackson Laboratory