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| Structural eye disease v0.76 | TCTN1 | Nicola Ragge reviewed gene: TCTN1: Rating: RED; Mode of pathogenicity: ; Publications: 21725307, 22693042; Phenotypes: Joubert syndrome 13, 614173; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.48 | TCTN1 | Ivone Leong edited their review of gene: TCTN1: Changed phenotypes: Joubert syndrome 13, 614173 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | TCTN1 | Ivone Leong reviewed gene: TCTN1: Rating: RED; Mode of pathogenicity: ; Publications: 21725307, 22693042; Phenotypes: Meckel syndrome 8, 613885, Joubert syndrome 24, 616654; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | TCTN1 |
Ivone Leong Source NHS GMS was added to TCTN1. Added phenotypes Joubert syndrome 13, 614173 for gene: TCTN1 Publications for gene TCTN1 were changed from 21725307; 22693042 to 22693042; 21725307 |
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| Structural eye disease v0.2 | TCTN1 |
Ellen McDonagh gene: TCTN1 was added gene: TCTN1 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: TCTN1 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: TCTN1 were set to 21725307; 22693042 Phenotypes for gene: TCTN1 were set to Joubert syndrome |
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