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This spontaneous T-to-C mutation (ChrX:g.161192220T>C) changes leucine codon 145 to a proline codon (p.L145P). It is found in the BALB/cJ, BALB/cByJ, CAST/EiJ, LEWES/EiJ, MOLF/EiJ, NOD/ShiLtJ, PWK/PhJ, SEA/GnJ, SPRET/EiJ, WSB/EiJ, and ZALENDE/EiJ strains. (J:294207)
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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References Literature
Title
PMID
Journal
Year
IF
