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A single T nucleotide insertion is located at position 945 in exon 6 (945T) creating a frameshift mutation resulting in a truncated protein due to a premature stop codon at the end of exon 6 at position 309 (K309*). This mutation is unique to BALB/cCrl and BALB/cAnNCrl strains and is not found in BALB/cJ derived strains. (J:177709)
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
