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| Structural eye disease v3.74 | CNGA1 | Arina Puzriakova Phenotypes for gene: CNGA1 were changed from Retinitis pigmentosa 49, 613756; Eye Disorders to Retinitis pigmentosa 49, OMIM:613756 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.76 | CNGA1 | Nicola Ragge reviewed gene: CNGA1: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 49, 613756; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | CNGA1 | Ivone Leong reviewed gene: CNGA1: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 49, 613756; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | CNGA1 |
Ivone Leong Source NHS GMS was added to CNGA1. Mode of inheritance for gene CNGA1 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Retinitis pigmentosa 49, 613756 for gene: CNGA1 |
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| Structural eye disease v0.2 | CNGA1 |
Ellen McDonagh gene: CNGA1 was added gene: CNGA1 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: CNGA1 was set to Phenotypes for gene: CNGA1 were set to Eye Disorders |
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