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| Structural eye disease v0.91 | TUBB | Nicola Ragge reviewed gene: TUBB: Rating: AMBER; Mode of pathogenicity: ; Publications: 26637975; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.89 | TUBB |
Ivone Leong Source NHS GMS was added to TUBB. Publications for gene TUBB were changed from to 26637975 |
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| Structural eye disease v0.88 | TUBB |
Ivone Leong Source Expert Review Amber was added to TUBB. Rating Changed from Red List (low evidence) to Amber List (moderate evidence) |
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| Structural eye disease v0.60 | TUBB | Mariya Moosajee reviewed gene: TUBB: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Skin Creases, Congenital Symmetric Circumferential, 2, CSCSC2; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.59 | TUBB |
Ivone Leong gene: TUBB was added gene: TUBB was added to Structural eye disease. Sources: London North GLH Mode of inheritance for gene: TUBB was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: TUBB were set to Skin Creases, Congenital Symmetric Circumferential, 2, CSCSC2, 156610 |
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