Activity
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| Fetal anomalies v8.26 | SEC23A | Ida Ertmanska commented on gene: SEC23A | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.25 | SEC23A | Tessa Homfray reviewed gene: SEC23A: Rating: AMBER; Mode of pathogenicity: ; Publications: 16980978, 38275611, 16980979, 21039434, 34580982, 26494538, 37828500, 27148587; Phenotypes: Craniolenticulosutural dysplasia, OMIM:607812, craniolenticulosutural dysplasia, MONDO:0011911; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.23 | SEC23A |
Ida Ertmanska gene: SEC23A was added gene: SEC23A was added to Fetal anomalies. Sources: Expert Review Amber,NHS GMS Mode of inheritance for gene: SEC23A was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: SEC23A were set to 16980978; 38275611; 16980979; 21039434; 34580982; 26494538; 37828500; 27148587 Phenotypes for gene: SEC23A were set to Craniolenticulosutural dysplasia, OMIM:607812; craniolenticulosutural dysplasia, MONDO:0011911 |
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