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Allele : Atp2b2<Deaf13> ATPase, Ca++ transporting, plasma membrane 2; deaf 13

Primary Identifier  MGI:5505458 Allele Type  Chemically induced (ENU)
Gene  Atp2b2 Inheritance Mode  Semidominant
Strain of Origin  BALB/c Is Recombinase  false
Is Wild Type  false
molecularNote  ENU mutagenesis induced a C to A point mutation in exon 9 that results in the amino acid substitution of serine for arginine at position 561 (R561S) in the catalytic core.
  • mutations:
  • Single point mutation
  • synonyms:
  • Deaf13Mrci,
  • Deaf13Mrci
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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

3 Publication categories

Trail: Allele