Activity
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| Fetal anomalies v4.192 | RPL15 |
Achchuthan Shanmugasundram Tag Q3_24_promote_green was removed from gene: RPL15. Tag Q3_24_NHS_review was removed from gene: RPL15. |
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| Fetal anomalies v4.192 | RPL15 | Achchuthan Shanmugasundram edited their review of gene: RPL15: Added comment: The rating of this gene has been updated to green and the mode of inheritance set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted following NHS Genomic Medicine Service approval.; Changed rating: GREEN; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v4.191 | RPL15 |
Achchuthan Shanmugasundram Source Expert Review Green was added to RPL15. Rating Changed from Amber List (moderate evidence) to Green List (high evidence) |
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| Fetal anomalies v4.89 | RPL15 |
Achchuthan Shanmugasundram Tag Q3_24_promote_green tag was added to gene: RPL15. Tag Q3_24_NHS_review tag was added to gene: RPL15. |
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| Fetal anomalies v4.36 | RPL15 | Achchuthan Shanmugasundram commented on gene: RPL15 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v4.35 | RPL15 | Lyn Chitty reviewed gene: RPL15: Rating: GREEN; Mode of pathogenicity: ; Publications: 23812780, 20301769, 29599205; Phenotypes: Diamond-Blackfan anemia 12, OMIM:615550, multiple congenital malformations, hydrops; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v4.34 | RPL15 |
Achchuthan Shanmugasundram gene: RPL15 was added gene: RPL15 was added to Fetal anomalies. Sources: Expert Review Amber,NHS GMS Mode of inheritance for gene: RPL15 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: RPL15 were set to 23812780; 20301769; 29599205 Phenotypes for gene: RPL15 were set to Diamond-Blackfan anemia 12, OMIM:615550; multiple congenital malformations; hydrops |
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