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Pulmonary arterial hypertension v2.16 | ABCC8 | Ivone Leong Tag to_be_confirmed_NHSE tag was added to gene: ABCC8. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Pulmonary arterial hypertension v2.9 | ABCC8 | Ivone Leong Tag for-review tag was added to gene: ABCC8. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Pulmonary arterial hypertension v2.9 | ABCC8 | Ivone Leong Classified gene: ABCC8 as Amber List (moderate evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Pulmonary arterial hypertension v2.9 | ABCC8 | Ivone Leong Added comment: Comment on list classification: New gene added by Zornitza Stark (Australian Genomics). This gene is associated with a phenotype in OMIM. There is enough evidence to support a gene-disease association. This gene should be rated Green at the next review. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Pulmonary arterial hypertension v2.9 | ABCC8 | Ivone Leong Gene: abcc8 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Pulmonary arterial hypertension v2.8 | ABCC8 | Ivone Leong Publications for gene: ABCC8 were set to 31406341; 30354297 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Pulmonary arterial hypertension v2.4 | ABCC8 |
Zornitza Stark gene: ABCC8 was added gene: ABCC8 was added to Pulmonary arterial hypertension. Sources: Expert list Mode of inheritance for gene: ABCC8 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: ABCC8 were set to 31406341; 30354297 Phenotypes for gene: ABCC8 were set to Diabetes mellitus; Hypoglycaemia; Pulmonary arterial hypertension Review for gene: ABCC8 was set to GREEN gene: ABCC8 was marked as current diagnostic Added comment: Twelve heterozygous variants identified in PAH cases. Included functional assessment and independent validation of the association with this gene. Sources: Expert list |