| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Transplant Co-Morbidity v1.0 | NBEAL2 | Gene migrated from ENSG00000160796 to ENSG00000160796 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Transplant Co-Morbidity v0.0 | NBEAL2 |
Bryony Thompson gene: NBEAL2 was added gene: NBEAL2 was added to Transplant Co-Morbidity Superpanel. Sources: Expert Review Green,Expert list Mode of inheritance for gene: NBEAL2 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: NBEAL2 were set to 21765412; 21765411; 21765413 Phenotypes for gene: NBEAL2 were set to Gray platelet syndrome, MIM# 139090 |
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