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Exon 11 was replaced with a modified exon 11 in which nucleotide substitutions (TCT to GCA) result in the amino acid substitution of alanine for serine at position 326 (S326A). Additional nucleotide substitutions also introduce an Afel restriction site into the exon. (J:197743)
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 |
|---|
References Literature
Title
PMID
Journal
Year
IF
