|  Help  |  About  |  Contact Us

Allele : Alb<em12Mvw> albumin; endonuclease-mediated mutation 12, Michael Wiles

Primary Identifier  MGI:5494605 Allele Type  Endonuclease-mediated
Attribute String  Null/knockout Gene  Alb
Strain of Origin  B6.Cg-Fcgrt<tm1Dcr> Tg(FCGRT)32Dcr/DcrJ Is Recombinase  false
Is Wild Type  false
molecularNote  Exon 4 was targeted by introduction of TALEN mRNA into fertilized B6.Cg-Fcgrttm1Dcr Tg(FCGRT)32Dcr/DcrJ oocytes and the resulting founder screened and found to have a 2 base pair deletion beginning at Chromosome 5 base 90,464,113 (GRCm38.p2) which is predicted to result in a frame shift then a premature stop codon 5 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:
  • Intragenic deletion
Quick Links:
 
Quick Links:
 

1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

3 Carried By

0 Driven By

6 Publication categories