Log In|Sign Up
EN
Exon 2 was replaced with a modified exon 2 in which the nucleotide substitutions (AGT to GCT) result in the amino acid substitution of alanine for serine at position 38 (S38A). This mutation is predicted not to interact with endogenous replication protein A. Cre-mediated recombination removed the floxed neomycin resistance cassette inserted upstream of the modified exon 2. (J:209271)
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
