Homologous recombination in C57BL/6 mouse embryonic stem cells was used to replace exon 12 with the orthologous human PAH exon 12 sequence including 500 bp of the flanking genomic sequence of both 5' and 3' of exon 12. Additionally, exon 12 also contains the amino acid substitution at position 408 altering arginine to tryptophan (R408W; c.1222 C to T) of the phenylalanine hydroxylase (Pah) gene on chromosome 10. The construct also included a loxP-flanked neomycin selection cassette upstream of exon 12 which was subsequently removed by crossing to Cre deleter. (J:344302)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
C57BL/6
Targeted
Insertion, Intragenic deletion
--
1
6
1

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

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PMID
Journal
Year
IF
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