|  Help  |  About  |  Contact Us

Allele : Crx<Rip> cone-rod homeobox; retina with immature photoreceptors

Primary Identifier  MGI:5515375 Allele Type  Spontaneous
Gene  Crx Inheritance Mode  Dominant
Strain of Origin  C57BL/6J Is Recombinase  false
Is Wild Type  false
molecularNote  A spontaneous 1-bp deletion in exon 4 introduces a frame shift mutation that skips the C-terminal Otx-like domain and adds 133 unrelated residues. Western blot analysis confirmed the expression of the larger (44 kDa) than normal (34 kDa) protein in the retina.
  • mutations:
  • Intragenic deletion
Quick Links:
 
Quick Links:
 

1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

0 Driven By

5 Publication categories