Mouse Genome Informatics
ht
    Prpf3Gt(RRO284)Byg/Prpf3+
involves: 129P2/OlaHsd * C57BL/6
Key:
phenotype observed in females WTSI Wellcome Trust Sanger Institute
phenotype observed in males EuPh Europhenome
N normal phenotype
       
vision/eye
N
• despite involvement of PRPF3 mutations in retinitis pigmentosa in humans, retinal function, morphology and ultrastructure are similar to controls (J:141780)

Mouse Models of Human Disease
OMIM IDRef(s)
NOT Retinitis Pigmentosa 18; RP18 601414 J:141780