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Allele : Pah<tm2.1(PAH*)Xiwan> phenylalanine hydroxylase; targeted mutation 2.1, Xiao Wang

Primary Identifier  MGI:7574745 Attribute String  Humanized sequence
Gene  Pah Transmission  Germline
Strain of Origin  C57BL/6 Is Recombinase  false
Is Wild Type  false
molecularNote  Homologous recombination in C57BL/6 mouse embryonic stem cells was used to replace exon 12 with the orthologous genomic DNA of human PAH from approximately 500 bp upstream of exon 10 through approximately 600 bp downstream of exon 12. The knockin human region included the c.1066-11G>A variant, introduced by alteration of the corresponding position in intron 11 from a G to an A. The construct also included a loxP-flanked neomycin selection cassette upstream of exon 12 which was subsequently removed by crossing to Cre deleter.
  • mutations:
  • Insertion,
  • Intragenic deletion
  • synonyms:
  • PAH c. 1066-11G>A,
  • PAH c. 1066-11G>A
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

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0 Driven By

3 Publication categories

Trail: Allele