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Allele : Prom1<rd19> prominin 1; retinal degeneration 19
Primary Identifier  MGI:5605699 Allele Type  Spontaneous
Attribute String  Null/knockout Gene  Prom1
Inheritance Mode  Recessive Strain of Origin  BXD83/RwwJ
Is Recombinase  false Is Wild Type  false
molecularNote  A single A-to-T transversion (on the negative gene strand; lower case in ATCAAACAGACCaAGGATGCCCTGCAGAAC) changes amino acid 268 from lysine to a stop codon (p.K268*).
  • mutations:
  • Single point mutation
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

0 Driven By

7 Publication categories





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