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Phenotypes Associated with This Genotype
Genotype
MGI:3820247
Allelic
Composition
Prpf3Gt(RRO284)Byg/Prpf3+
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Prpf3Gt(RRO284)Byg mutation (0 available); any Prpf3 mutation (12 available)
phenotype observed in females
phenotype observed in males
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)
• 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 ID Ref(s)
NOT Retinitis Pigmentosa 18; RP18 601414 J:141780


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
02/02/2016
MGI 6.02
The Jackson Laboratory