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| Fetal anomalies v8.26 | NCKAP1 | Ida Ertmanska commented on gene: NCKAP1 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.25 | NCKAP1 | Natalie Canham reviewed gene: NCKAP1: Rating: RED; Mode of pathogenicity: ; Publications: 41462819; Phenotypes: congenital heart disease, MONDO:0005453, neurodevelopmental disorder, MONDO:0700092; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.23 | NCKAP1 |
Ida Ertmanska gene: NCKAP1 was added gene: NCKAP1 was added to Fetal anomalies. Sources: NHS GMS,Expert Review Red Mode of inheritance for gene: NCKAP1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: NCKAP1 were set to 41462819 Phenotypes for gene: NCKAP1 were set to congenital heart disease, MONDO:0005453; neurodevelopmental disorder, MONDO:0700092 |
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