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Allele : Crygs<rncat> crystallin, gamma S; recessive nuclear cataract

Primary Identifier  MGI:2181679 Allele Type  Spontaneous
Gene  Crygs Inheritance Mode  Recessive
Strain of Origin  Kunming Is Recombinase  false
Is Wild Type  false
molecularNote  The mutation is a G to A transition point mutation at position 489 in exon 3. This alters codon 163 from one encoding a tryptophan to a stop codon, resulting in premature truncation of the last 16 amino acids of the protien.
  • mutations:
  • Single point mutation
  • synonyms:
  • rncat,
  • rncat
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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

4 Publication categories