Missense mutations at codons 207 and 208 were introduced at the endogenous locus via homologous recombination. The mutations were designed to substitute a glutamate (207) and glycine (208) with alanine residues. A floxed neo cassette was integrated upstream in intron 2 for selection. Mice carrying this allele were used to generate Esr1tm1.1Lja. (J:79228)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
129P2/OlaHsd-Hprt1b-m3
Targeted
Insertion, Nucleotide substitutions
--
1
4
2

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

References Literature

Title
PMID
Journal
Year
IF
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