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| Structural eye disease v0.76 | PRPF31 | Nicola Ragge reviewed gene: PRPF31: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 11, 600138; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.76 | PRPF3 | Nicola Ragge reviewed gene: PRPF3: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 18, 601414; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.48 | PRPF31 | Ivone Leong edited their review of gene: PRPF31: Changed phenotypes: Retinitis pigmentosa 11, 600138 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.48 | PRPF3 | Ivone Leong edited their review of gene: PRPF3: Changed phenotypes: Retinitis pigmentosa 18, 601414 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | PRPF31 | Ivone Leong reviewed gene: PRPF31: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 60, 613983; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | PRPF3 | Ivone Leong reviewed gene: PRPF3: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 11, 600138; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | PRPF31 |
Ivone Leong Source NHS GMS was added to PRPF31. Mode of inheritance for gene PRPF31 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Added phenotypes Retinitis pigmentosa 11, 600138 for gene: PRPF31 |
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| Structural eye disease v0.15 | PRPF3 |
Ivone Leong Source NHS GMS was added to PRPF3. Mode of inheritance for gene PRPF3 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Added phenotypes Retinitis pigmentosa 18, 601414 for gene: PRPF3 |
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| Structural eye disease v0.2 | PRPF31 |
Ellen McDonagh gene: PRPF31 was added gene: PRPF31 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: PRPF31 was set to Phenotypes for gene: PRPF31 were set to Eye Disorders |
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| Structural eye disease v0.2 | PRPF3 |
Ellen McDonagh gene: PRPF3 was added gene: PRPF3 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: PRPF3 was set to Phenotypes for gene: PRPF3 were set to Eye Disorders |
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