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19 Jun 2019	Structural eye disease v0.76	CABP4	Nicola Ragge reviewed gene: CABP4: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Night blindness, congenital stationary (incomplete), 2B, autosomal recessive, 610427; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
17 Apr 2019	Structural eye disease v0.38	CABP4	Ivone Leong reviewed gene: CABP4: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Night blindness, congenital stationary (incomplete), 2B, autosomal recessive, 610427; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
17 Apr 2019	Structural eye disease v0.15	CABP4	Ivone Leong Source NHS GMS was added to CABP4. Mode of inheritance for gene CABP4 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Night blindness, congenital stationary (incomplete), 2B, autosomal recessive, 610427 for gene: CABP4
03 Jan 2019	Structural eye disease v0.2	CABP4	Ellen McDonagh gene: CABP4 was added gene: CABP4 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: CABP4 was set to Phenotypes for gene: CABP4 were set to Eye Disorders