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Cholestasis v0.21 | UGT1A1 | Ivone Leong Marked gene: UGT1A1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Cholestasis v0.21 | UGT1A1 | Ivone Leong Added comment: Comment when marking as ready: As discussed in the GMS Gastrohepatology Specialist Test Group webex call 14th Jan 2019: The Specialist Test Group agreed that there is enough evidence to rate this gene green. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Cholestasis v0.21 | UGT1A1 | Ivone Leong Gene: ugt1a1 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Cholestasis v0.10 | UGT1A1 |
Ivone Leong Source Other was added to UGT1A1. Mode of inheritance for gene UGT1A1 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes [Gilbert syndrome] 143500; Crigler-Najjar syndrome, type I 218800; Neonatal and Adult Cholestasis; Crigler-Najjar syndrome, type II 606785; unconjugated jaundice for gene: UGT1A1 Publications for gene UGT1A1 were changed from to 11013440 |
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Cholestasis v0.4 | UGT1A1 |
Ivone Leong Source Expert Review Green was added to UGT1A1. Rating Changed from Red List (low evidence) to Green List (high evidence) |
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Cholestasis v0.3 | UGT1A1 | Ivone Leong reviewed gene: UGT1A1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Cholestasis v0.2 | UGT1A1 |
Ivone Leong gene: UGT1A1 was added gene: UGT1A1 was added to Cholestasis. Sources: NHS GMS Mode of inheritance for gene: UGT1A1 was set to |