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Allele : Psap<tm3.1Ggb> prosaposin; targeted mutation 3.1, Gregory A Grabowski

Primary Identifier  MGI:4418521 Allele Type  Targeted
Attribute String  Not Specified Gene  Psap
Transmission  Germline Strain of Origin  129S/SvEv
Is Recombinase  false Is Wild Type  false
molecularNote  A nucleotide substitution was created that results in changing cysteine codon 5 (with respect to Saposin C) in exon 11 to proline and a loxP site flanked neomycin resistance gene cassette was inserted into intron 9. The neo cassette was removed through subsequent Cre-mediated recombination. The mutation eliminates one of the encoded protein's three disulfide bridges and results in a selective deficiency in Saposin C. The absence of Saposin C was confirmed by western blot analysis on homozygous fibroblasts; the expression of Saposin A, B and D (the other forms post-translationally generated from this locus) was not affected.
  • mutations:
  • Nucleotide substitutions
  • synonyms:
  • Psap<C->,
  • Psap<C->
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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

9 Publication categories

Trail: Allele