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| Structural eye disease v0.76 | RGS9BP | Nicola Ragge reviewed gene: RGS9BP: Rating: RED; Mode of pathogenicity: Other - please provide details in the comments; Publications: ; Phenotypes: Bradyopsia, 608415; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.48 | RGS9BP | Ivone Leong edited their review of gene: RGS9BP: Changed phenotypes: Bradyopsia, 608415 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | RGS9BP | Ivone Leong reviewed gene: RGS9BP: Rating: RED; Mode of pathogenicity: Other - please provide details in the comments; Publications: ; Phenotypes: Retinitis pigmentosa 4, autosomal dominant or recessive, 613731, Night blindness, congenital stationary, autosomal dominant 1, 610445, Fundus albipunctatus, 136880; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | RGS9BP |
Ivone Leong Source NHS GMS was added to RGS9BP. Mode of inheritance for gene RGS9BP was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Bradyopsia, 608415 for gene: RGS9BP |
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| Structural eye disease v0.2 | RGS9BP |
Ellen McDonagh gene: RGS9BP was added gene: RGS9BP was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: RGS9BP was set to Phenotypes for gene: RGS9BP were set to Eye Disorders |
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