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Allele : Mfrp<rd6> membrane frizzled-related protein; retinal degeneration 6

Primary Identifier  MGI:1888705 Allele Type  Spontaneous
Gene  Mfrp Inheritance Mode  Recessive
Strain of Origin  C3fBAnl.Cg-Cat<b>/AnlJ Is Recombinase  false
Is Wild Type  false
molecularNote  The rd6 mutation was identified as a 4 bp deletion in the splice donor sequence of intron 4 in the Mfrp gene. The mutation results in the skipping of exon 4. While the mutation does not cause a frameshift, 58 amino acids are deleted from the protein.
  • mutations:
  • Intragenic deletion
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

6 Carried By

0 Driven By

14 Publication categories