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19 Jun 2019	Structural eye disease v0.76	C1QTNF5	Nicola Ragge reviewed gene: C1QTNF5: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinal degeneration, late-onset, autosomal dominant, 605670; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
17 Apr 2019	Structural eye disease v0.38	C1QTNF5	Ivone Leong reviewed gene: C1QTNF5: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinal degeneration, late-onset, autosomal dominant, 605670; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes
17 Apr 2019	Structural eye disease v0.15	C1QTNF5	Ivone Leong Source NHS GMS was added to C1QTNF5. Mode of inheritance for gene C1QTNF5 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Added phenotypes Retinal degeneration, late-onset, autosomal dominant, 605670 for gene: C1QTNF5
03 Jan 2019	Structural eye disease v0.2	C1QTNF5	Ellen McDonagh gene: C1QTNF5 was added gene: C1QTNF5 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: C1QTNF5 was set to Phenotypes for gene: C1QTNF5 were set to Eye Disorders