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Allele : Alb<em8Mvw> albumin; endonuclease-mediated mutation 8, Michael Wiles

Primary Identifier  MGI:5494601 Allele Type  Endonuclease-mediated
Attribute String  Null/knockout Gene  Alb
Strain of Origin  C57BL/6J Is Recombinase  false
Is Wild Type  false
molecularNote  Exon 4 was targeted by introduction of TALEN mRNA into fertilized C57BL/6J oocytes and the resulting founder screened and found to have a 1 base pair deletion at Chromosome 5 base 90,464,113 (GRCm38.p2) which is predicted to result in a frame shift then a premature stop codon 55 amino acids downstream of the encoded frame shift. By ELISA, heterozgyotes have a decrease in serum albumin of approximately 30 percent and homozygotes have no detectable serum albumin.
  • mutations:
  • Single point mutation,
  • Intragenic deletion
  • synonyms:
  • Alb-,
  • Alb-
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

Trail: Allele

0 Driven By

9 Publication categories

Trail: Allele