Activity
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8 actions
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| Fetal anomalies v5.80 | KDM2B | Achchuthan Shanmugasundram Tag gene-checked tag was added to gene: KDM2B. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v5.78 | KDM2B |
Achchuthan Shanmugasundram Tag Q1_25_ NHS_review was removed from gene: KDM2B. Tag Q1_25_ promote_green was removed from gene: KDM2B. |
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| Fetal anomalies v5.78 | KDM2B | Achchuthan Shanmugasundram edited their review of gene: KDM2B: 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 v5.77 | KDM2B |
Achchuthan Shanmugasundram Source Expert Review Green was added to KDM2B. Rating Changed from Amber List (moderate evidence) to Green List (high evidence) |
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| Fetal anomalies v5.74 | KDM2B |
Achchuthan Shanmugasundram Tag Q1_25_ NHS_review tag was added to gene: KDM2B. Tag Q1_25_ promote_green tag was added to gene: KDM2B. |
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| Fetal anomalies v5.16 | KDM2B | Achchuthan Shanmugasundram commented on gene: KDM2B | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v5.15 | KDM2B | Natalie Chandler reviewed gene: KDM2B: Rating: GREEN; Mode of pathogenicity: ; Publications: 36322151; Phenotypes: Neurodevelopmental disorder MONDO#0700092, KDM2B-related; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v5.13 | KDM2B |
Achchuthan Shanmugasundram gene: KDM2B was added gene: KDM2B was added to Fetal anomalies. Sources: NHS GMS,Expert Review Amber Mode of inheritance for gene: KDM2B was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: KDM2B were set to 36322151 Phenotypes for gene: KDM2B were set to Neurodevelopmental disorder MONDO:0700092, KDM2B-related |
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