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Rare multisystem ciliopathy disorders v1.86 ARMC9 Rebecca Foulger Classified gene: ARMC9 as Green List (high evidence)
Rare multisystem ciliopathy disorders v1.86 ARMC9 Rebecca Foulger Added comment: Comment on list classification: Updated rating from Green to Red. Confirmed Disease confidence rating in DDG2P for Joubert syndrome 30. Green rating by Zornitza Stark and Olivia Niblock. Sufficient cases to support causation from PMID:28625504: In 11 patients from 8 unrelated families with Joubert syndrome-30 (MIM:617622), Van De Weghe et al. (2017, PMID:28625504) identified 10 different homozygous or compound heterozygous variants in the ARMC9 gene. Variants in the first 2 families were found by WES of 53 patients from 51 families with a clinical diagnosis of Joubert syndrome. Variants in 3 additional unrelated patients were found by targeted sequencing of the ARMC9 gene, and the remaining 2 families were ascertained from a cohort of Saudi Arabian families who underwent exome sequencing.
Rare multisystem ciliopathy disorders v1.86 ARMC9 Rebecca Foulger Gene: armc9 has been classified as Green List (High Evidence).
Rare multisystem ciliopathy disorders v1.85 ARMC9 Rebecca Foulger Phenotypes for gene: ARMC9 were changed from Joubert syndrome to Joubert syndrome 30, 617622
Rare multisystem ciliopathy disorders ARMC9 Zornitza Stark reviewed gene: ARMC9
Rare multisystem ciliopathy disorders ARMC9 Olivia Niblock added ARMC9 to panel
Rare multisystem ciliopathy disorders ARMC9 Olivia Niblock reviewed ARMC9