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| Structural eye disease v0.91 | WNT3 | Nicola Ragge reviewed gene: WNT3: Rating: RED; Mode of pathogenicity: ; Publications: 14872406; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.89 | WNT3 |
Ivone Leong Source NHS GMS was added to WNT3. Source Expert Review Red was added to WNT3. Publications for gene WNT3 were changed from to 14872406 Rating Changed from Amber List (moderate evidence) to Red List (low evidence) |
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| Structural eye disease v0.88 | WNT3 |
Ivone Leong Source Expert Review Amber was added to WNT3. Rating Changed from Red List (low evidence) to Amber List (moderate evidence) |
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| Structural eye disease v0.60 | WNT3 | Mariya Moosajee reviewed gene: WNT3: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Tetraamelia Syndrome 1, TETAMS1; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.59 | WNT3 |
Ivone Leong gene: WNT3 was added gene: WNT3 was added to Structural eye disease. Sources: London North GLH Mode of inheritance for gene: WNT3 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: WNT3 were set to Tetraamelia Syndrome 1, TETAMS1, 273395 |
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