Activity
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3 actions
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| Fetal anomalies v5.16 | ZNF687 | Achchuthan Shanmugasundram commented on gene: ZNF687 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v5.15 | ZNF687 | Vicki Harrison reviewed gene: ZNF687: Rating: RED; Mode of pathogenicity: ; Publications: 29493781, 26849110; Phenotypes: Paget disease of bone 6, MIM#616833; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v5.13 | ZNF687 |
Achchuthan Shanmugasundram gene: ZNF687 was added gene: ZNF687 was added to Fetal anomalies. Sources: NHS GMS,Expert Review Red Mode of inheritance for gene: ZNF687 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: ZNF687 were set to 26849110; 29493781 Phenotypes for gene: ZNF687 were set to Paget disease of bone 6, OMIM:616833 |
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