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Tryptophan codon 1988 (TGG) in exon 37 was changed to arginine (CGG) (p.W1988R). This mutation is the equivalent of the human p.W1989R mutation found in some bipolar disorder (BD) patients. A loxP site flanked neomycin resistance gene cassette that was inserted into an intron was removed through subsequent Cre-mediated recombination. (J:329513)
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
