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| Structural eye disease v1.94 | RAB3GAP2 | Arina Puzriakova Phenotypes for gene: RAB3GAP2 were changed from Martsolf syndrome, 212720; Warburg micro syndrome 2, 614225; Martsolf syndrome, 212720Warburg micro syndrome 2, 614225; Warburg Micro Syndrome to Martsolf syndrome 1, OMIM:212720; Warburg micro syndrome 2, OMIM:614225 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.76 | RAB3GAP2 | Nicola Ragge reviewed gene: RAB3GAP2: Rating: GREEN; Mode of pathogenicity: ; Publications: 23420520; Phenotypes: Martsolf syndrome, 212720Warburg micro syndrome 2, 614225, Warburg Micro Syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | RAB3GAP2 | Ivone Leong reviewed gene: RAB3GAP2: Rating: GREEN; Mode of pathogenicity: ; Publications: 23420520; Phenotypes: Martsolf syndrome, 212720, Warburg micro syndrome 2, 614225, Warburg Micro Syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | RAB3GAP2 |
Ivone Leong Source NHS GMS was added to RAB3GAP2. Added phenotypes Martsolf syndrome, 212720; Warburg micro syndrome 2, 614225; Warburg Micro Syndrome for gene: RAB3GAP2 Publications for gene RAB3GAP2 were changed from to 23420520 |
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| Structural eye disease v0.2 | RAB3GAP2 |
Ellen McDonagh gene: RAB3GAP2 was added gene: RAB3GAP2 was added to Structural eye disease. Sources: Expert Review Green Mode of inheritance for gene: RAB3GAP2 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: RAB3GAP2 were set to Martsolf syndrome, 212720Warburg micro syndrome 2, 614225; Warburg Micro Syndrome |
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