Activity
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| Fetal anomalies v8.26 | LOXL3 | Ida Ertmanska commented on gene: LOXL3 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.25 | LOXL3 | Sarah Graham reviewed gene: LOXL3: Rating: AMBER; Mode of pathogenicity: ; Publications: 34787502, 30362103, 36610533, 26307084, 41052910, 38957076, 26957899, 25663169; Phenotypes: Stickler syndrome, MONDO:0019354; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.23 | LOXL3 |
Ida Ertmanska gene: LOXL3 was added gene: LOXL3 was added to Fetal anomalies. Sources: Expert Review Amber,NHS GMS Mode of inheritance for gene: LOXL3 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: LOXL3 were set to 34787502; 30362103; 36610533; 26307084; 41052910; 38957076; 26957899; 25663169 Phenotypes for gene: LOXL3 were set to Stickler syndrome, MONDO:0019354 |
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