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Allele : Cryge<Elo> crystallin, gamma E; eye lens obsolescence

Primary Identifier  MGI:1857599 Allele Type  Spontaneous
Attribute String  Dominant negative Gene  Cryge
Inheritance Mode  Semidominant Strain of Origin  (C57BL/6JNga x Japanese fancy mouse (Oca2<p>))F4
Is Recombinase  false Is Wild Type  false
molecularNote  A single base (G) deletion at nucleotide position 403 (codon 135) in the fourth ""Greek key"" motif of the Cryge gene product, causes a frameshift mutation that can translate for another 11 amino acids before prematurely terminating (codon 146). The truncated peptide lacking the fourth ""Greek key"" probably leads to misfolding of the crystallin gene product and may act as a dominant negative.
  • mutations:
  • Intragenic deletion
  • synonyms:
  • Cryge<Cat2-Elo>,
  • ELO,
  • Cryge<Cat2-Elo>,
  • ELO
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

7 Carried By

Trail: Allele

0 Driven By

8 Publication categories

Trail: Allele