Log In|Sign Up
EN
ENU-induced G to T transversion at base pair 23,757,026 (v38) on chromosome 11, or base pair 13,945 in the GenBank genomic region NC_000077. The mutation corresponds to residue 456 in the mRNA sequence NM_009044 within exon 3 of 10 total exons. The mutation results in substitution of glycine 59 for a premature stop codon (G59*) in the c-Rel protein. (J:272778)
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：
Show/Hide columns
| Phenotypes |
|---|
References Literature
Title
PMID
Journal
Year
IF
