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EN
ENU treatment induced an A-to-T transversion at base pair 121,228,606 (GRCm38) on chromosome 2, or base pair 61,720 in the GenBank genomic region NC_000068 encoding Trp53bp1. The mutation corresponds to residue 2,902 in the mRNA sequence NM_013735 within exon 13 of 28 total exons. The mutation results in substitution of arginine 925 with a stop codon (p.R925*) in the protein. (J:272848)
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
