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| Structural eye disease v0.76 | CERKL | Nicola Ragge reviewed gene: CERKL: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 26, 608380; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | CERKL | Ivone Leong reviewed gene: CERKL: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 26, 608380; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | CERKL |
Ivone Leong Source NHS GMS was added to CERKL. Mode of inheritance for gene CERKL was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Retinitis pigmentosa 26, 608380 for gene: CERKL |
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| Structural eye disease v0.2 | CERKL |
Ellen McDonagh gene: CERKL was added gene: CERKL was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: CERKL was set to Phenotypes for gene: CERKL were set to Eye Disorders |
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