This mutation comprises a T to G transversion at the +2 position of the seventh intron, which results in the generation of transcripts lacking exon 7 and instead containing 50 novel C-terminal amino acids preceding a premature termination codon. The absence of protein expression was confirmed by western blot analysis on brain extracts. (J:148877)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
BALB/cAnN
Chemically induced
Single point
Dominant
1
6
2

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
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