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Allele : Rgs18<m1H> regulator of G-protein signaling 18; mutation 1, Harwell

Primary Identifier  MGI:5307901 Allele Type  Chemically induced (ENU)
Attribute String  Null/knockout Gene  Rgs18
Inheritance Mode  Recessive Strain of Origin  BALB/cAnN
Is Recombinase  false Is Wild Type  false
Project Collection  Harwell ENU Mutagenesis
molecularNote  The mutation was identified in a screen of the Harwell ENU mutant archive for mutations in this gene. The molecular lesion is a T to A (TAT to TAA) mutation that results in a premature stop codon (Y139STOP) in exon 4. Western blot analysis confirmed the absence of protein expression in platelet extracts from homozygous mutant mice.
  • mutations:
  • Single point mutation
  • synonyms:
  • RGS18<->,
  • BHV48,
  • BHV48,
  • RGS18<->
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

2 Carried By

0 Driven By

4 Publication categories