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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Sarm1tm1Aidi
targeted mutation 1, Aihao Ding
MGI:3765956
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Sarm1tm1Aidi/Sarm1tm1Aidi involves: 129X1/SvJ * C57BL/6J MGI:3765957
cx2
Sarm1tm1Aidi/Sarm1tm1Aidi
Stmn2em1Jmi/Stmn2em1Jmi
involves: 129X1/SvJ * C57BL/6J * C57BL/6N MGI:7523312


Genotype
MGI:3765957
hm1
Allelic
Composition
Sarm1tm1Aidi/Sarm1tm1Aidi
Genetic
Background
involves: 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Sarm1tm1Aidi mutation (1 available); any Sarm1 mutation (25 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• in response to oxygen and glucose deprivation, hippocampus cells exhibit reduced apoptosis (31.89+/-3.34% compared to 67.21+/-5.10% in wild-type cells)

immune system
N
• macrophages exhibit normal function




Genotype
MGI:7523312
cx2
Allelic
Composition
Sarm1tm1Aidi/Sarm1tm1Aidi
Stmn2em1Jmi/Stmn2em1Jmi
Genetic
Background
involves: 129X1/SvJ * C57BL/6J * C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Sarm1tm1Aidi mutation (1 available); any Sarm1 mutation (25 available)
Stmn2em1Jmi mutation (0 available); any Stmn2 mutation (41 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• at 3 months of age, mice show a decrease in the latency time (s) to fall from an inverted screen that is similar to that in single Stmn2em1Jmi homozygotes, indicating severe motor function impairment

nervous system
• lumbrical muscle NMJs exhibit presynaptic and postsynaptic elements that are indistinguishable from those of single Stmn2em1Jmi homozygotes, including endplate fragmentation and many regions of partial innervation





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