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Cholestasis v1.81 TMEM67 Arina Puzriakova Tag curated_removed tag was added to gene: TMEM67.
Cholestasis v1.18 TMEM67 Ivone Leong Classified gene: TMEM67 as No list
Cholestasis v1.18 TMEM67 Ivone Leong Added comment: Comment on list classification: This gene has been downgraded from Green to Grey based on expert review from Miranda Durkie (Genetics).
Cholestasis v1.18 TMEM67 Ivone Leong Gene: tmem67 has been removed from the panel.
Cholestasis v1.17 TMEM67 Ivone Leong Tag for-review was removed from gene: TMEM67.
Cholestasis v1.16 TMEM67 Zornitza Stark reviewed gene: TMEM67: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Cholestasis v1.8 TMEM67 Ivone Leong Tag for-review tag was added to gene: TMEM67.
Cholestasis v1.4 TMEM67 Miranda Durkie reviewed gene: TMEM67: Rating: RED; Mode of pathogenicity: ; Publications: 28680603; Phenotypes: ; Mode of inheritance:
Cholestasis v0.15 TMEM67 Ivone Leong Marked gene: TMEM67 as ready
Cholestasis v0.15 TMEM67 Ivone Leong Gene: tmem67 has been classified as Green List (High Evidence).
Cholestasis v0.15 TMEM67 Ivone Leong Classified gene: TMEM67 as Green List (high evidence)
Cholestasis v0.15 TMEM67 Ivone Leong Added comment: Comment on list classification: 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. Promoted from amber to green.
Cholestasis v0.15 TMEM67 Ivone Leong Gene: tmem67 has been classified as Green List (High Evidence).
Cholestasis v0.11 TMEM67 Ivone Leong gene: TMEM67 was added
gene: TMEM67 was added to Cholestasis. Sources: NHS GMS
Mode of inheritance for gene: TMEM67 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: TMEM67 were set to 28680603; 16415887; 26191240; 19058225
Phenotypes for gene: TMEM67 were set to COACH syndrome (216360); {Bardet-Biedl syndrome 14, modifier of} (615991); Nephronophthisis 11 (613550); Meckel syndrome 3 (607361); Joubert syndrome 6 (310688); congenital hepatic fibrosis