Phenotype: Retinitis pigmentosa 1


OMIM: 180100
Inheritance: Multiple
Classification: Diseases of the eye and adnexa

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RP1 || c.1625C>G

Gene/Locus:    RP1
Dna Change:    c.1625C>G
Protein Change:    p.Ser542X
Mutation Type:    Substitution
Mutation Effect:    Nonsense
Location:    exon 4
Transcript:    NM_006269.1

PopulationEthnic GroupRegionMutation FrquencyCoalescence TimeReference
SpainNANA4.5% (11 families/244 unrelated families)NAAvila-Fernandez A et al., 2012Avila-Fernandez A, Corton M, Nishiguchi KM, Muñoz-Sanz N, Benavides-Mori B, Blanco-Kelly F, Riveiro-Alvarez R, Garcia-Sandoval B, Rivolta C, Ayuso C, . Identification of an RP1 prevalent founder mutation and related phenotype in Spanish patients with early-onset autosomal recessive retinitis.. Ophthalmology. 2012; 119(12):2616-21

References

Avila-Fernandez A, Corton M, Nishiguchi KM, Muñoz-Sanz N, Benavides-Mori B, Blanco-Kelly F, Riveiro-Alvarez R, Garcia-Sandoval B, Rivolta C, Ayuso C, Identification of an RP1 prevalent founder mutation and related phenotype in Spanish patients with early-onset autosomal recessive retinitis.Ophthalmology. 2012; 119(12):2616-21