Tg(SOD1*G37R)106Dpr
Alias:
SOD1G37R
Tg(SOD1-G37R)106Dpr
Tg(SOD1-G37R)106Pcw
Tg(SOD1G37R)106Pcw
Basic Information
Phenotypes
References
A 12 kb genomic DNA fragment containing a mutated form of human SOD1 with a glycine to arginine substitution at amino acid 37 (G37R) was used for the transgene. The G37R mutation is found in some cases of familial amyotrophic lateral sclerosis (FALS). (J:69178)
Basic Information
MGI ID
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
Related Disease
Reference
(C57BL/6J x C3H/HeJ)F2
--
Insertion
--
1
--
9
Phenotypes
Legend:
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes:
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Phenotypes
References
Title
PMID
Journal
Year
IF
No Data Found!
Comparison
Al agent
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