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An aspartate to asparagine missense mutation (D238N) was introduced into the C2A domain via homologous recombination. The mutation was made in the C2A domain. Western blot of brain homogenates from homozygous mutant animals verified the presence of protein expression. (J:79208)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
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 |
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References Literature
Title
PMID
Journal
Year
IF
