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| Structural eye disease v0.79 | TMEM237 | Ivone Leong Classified gene: TMEM237 as Green List (high evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.79 | TMEM237 | Ivone Leong Added comment: Comment on list classification: Promoted from amber to green based on expert review. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.79 | TMEM237 | Ivone Leong Gene: tmem237 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.76 | TMEM237 | Nicola Ragge reviewed gene: TMEM237: Rating: GREEN; Mode of pathogenicity: ; Publications: 22152675, 30055837 ; Phenotypes: Joubert syndrome 14, 614424; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.48 | TMEM237 | Ivone Leong edited their review of gene: TMEM237: Changed phenotypes: Joubert syndrome 14, 614424 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | TMEM237 | Ivone Leong reviewed gene: TMEM237: Rating: GREEN; Mode of pathogenicity: ; Publications: 22152675, 30055837 ; Phenotypes: COACH syndrome, 216360, Joubert syndrome 6, 610688, Meckel syndrome 3, 607361, Nephronophthisis 11, 613550, {Bardet-Biedl syndrome 14, modifer of}, 615991; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | TMEM237 |
Ivone Leong Source NHS GMS was added to TMEM237. Source Expert Review Amber was added to TMEM237. Added phenotypes Joubert syndrome 14, 614424 for gene: TMEM237 Publications for gene TMEM237 were changed from 22152675 to 30055837; 22152675 Rating Changed from Red List (low evidence) to Amber List (moderate evidence) |
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| Structural eye disease v0.2 | TMEM237 |
Ellen McDonagh gene: TMEM237 was added gene: TMEM237 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: TMEM237 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: TMEM237 were set to 22152675 Phenotypes for gene: TMEM237 were set to Joubert syndrome |
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