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This allele contains the following spontaneous mutation(s) that have a predicted consequential effect on the encoded peptide and that are specific to (fixed in) the MSN (Madison) strain used as a mania model, as compared to: the Hsd:ICR strain from which it is derived; the MaD2 (Maternal Defense 2) strain, which is also derived from Hsd:ICR but wasn't selected for mania; the C57BL/6J reference strain. Build GRCm38 genomic coordinates: g.chr11:59000521C>CTGG (p.P7061dup); g.chr11:59000884C>T (p.V6941M); g.chr11:59076137G>A (p.H3164Y). (J:267654)
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
