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This spontaneous C-to-G mutation (on reverse gene strand; chrX:g.163979223G>C on forward strand) changes proline codon 308 to an alanine codon (p.P308A). It is found in the AKR/J, BALB/cJ, BALB/cByJ, MOLF/EiJ, PWK/PhJ, RF/J, SEA/GnJ, SPRET/EiJ, and WSB/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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| Phenotypes |
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References Literature
Title
PMID
Journal
Year
IF
