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| Fetal anomalies v2.0 | NUBP2 | Gene migrated from ENSG00000095906 to ENSG00000095906 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v1.493 | Zornitza Stark Copied gene NUBP2 from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v1.493 | NUBP2 |
Zornitza Stark gene: NUBP2 was added gene: NUBP2 was added to Fetal anomalies. Sources: Expert Review Amber,Literature Mode of inheritance for gene: NUBP2 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: NUBP2 were set to 39867373 Phenotypes for gene: NUBP2 were set to Neurodevelopmental disorder, MONDO:0700092 |
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