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Allele : Cftr<tm1Unc> cystic fibrosis transmembrane conductance regulator; targeted mutation 1, University of North Carolina

Primary Identifier  MGI:1856709 Allele Type  Targeted
Attribute String  Null/knockout Gene  Cftr
Transmission  Germline Strain of Origin  129P2/OlaHsd
Is Recombinase  false Is Wild Type  false
description  Epithelial tissue from the gastrointestinal tract and airways exhibit abnormal cyclic AMP-mediated chloride ion transport similar to that observed in CF patients (J:23817).
molecularNote  A neomycin selection cassette was inserted into exon 11 (exon 10 in legacy nomenclature numbering) at sequences corresponding to codon 489 of the encoded protein. The authors predict that a truncated protein with amino acid 488 changed from isoleucine to alanine and a stop codon at position 489 are produced from this allele.
  • mutations:
  • Insertion
  • synonyms:
  • S489X,
  • Cftr-.ko,
  • UNC,
  • cftr<m1UNC>,
  • mCFTR<->,
  • Cftr<UNC>,
  • UNC,
  • Cftr-,
  • Cftr<UNC>,
  • mCFTR<->,
  • CFTR S489X-,
  • p.S489*,
  • p.S489*,
  • S489X,
  • CFTR S489X-,
  • Cftr-,
  • cftr<m1UNC>,
  • Cftr-.ko
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

13 Carried By

0 Driven By

276 Publication categories