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Allele : Lbr<ic> lamin B receptor; ichthyosis

Primary Identifier  MGI:1856063 Allele Type  Spontaneous
Gene  Lbr Inheritance Mode  Recessive
Strain of Origin  Not Specified Is Recombinase  false
Is Wild Type  false
molecularNote  A spontaneous mutation that arose in a sib-mated stock at Edinburgh in 1948. The mutation in the ic mouse was identified as a transition (523C>T) that introduces a premature stop codon at the glutamine codon at position 175 (p.Q175*).
  • mutations:
  • Single point mutation
  • synonyms:
  • ic,
  • ic
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

15 Publication categories