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This mutation is exclusive to the BALB/cByJ sub-strain and not found in BALB/cJ or any other strain tested. It is a C-to-T (g.X:74309969C>T) mutation that changes arginine codon 276 to a cysteine codon (p.R276C) (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
