|  Help  |  About  |  Contact Us

Allele : Clcn7<tm4.1Tjj> chloride channel, voltage-sensitive 7; targeted mutation 4.1, Thomas J Jentsch

Primary Identifier  MGI:4459519 Allele Type  Targeted
Gene  Clcn7 Transmission  Germline
Strain of Origin  (129X1/SvJ x 129S1/Sv)F1-Kitl<+> Is Recombinase  false
Is Wild Type  false
molecularNote  Nucleotide substitutions result in the amino acid substitution of alanine for glutamic acid at position 245 (E245A). This mutation is predicted to uncouple the chloride ion conduction from the proton exchanger function. An frt flanked neo cassette inserted upstream of exon 8 was removed by flp mediated recombination.
  • mutations:
  • Insertion,
  • Nucleotide substitutions
  • synonyms:
  • Clcn7<unc>,
  • Clcn7<E245A>,
  • Clcn7<E245A>,
  • Clcn7<unc>
Quick Links:
 
Quick Links:
 

1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

6 Publication categories