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EN
ENU mutagenesis generated a nucleotide substitution that resulted in an amino acid substitution of a STOP codon for serine at position 321 (S321X). This mutation is predicted to cause a premature truncation of the protein similar to one found in human patients with FOXP2-related speech and language difficulties (R328X). (J:135404)
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
