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Bleeding and Platelet Disorders v1.58 STAB2 Zornitza Stark Marked gene: STAB2 as ready
Bleeding and Platelet Disorders v1.58 STAB2 Zornitza Stark Gene: stab2 has been classified as Red List (Low Evidence).
Bleeding and Platelet Disorders v1.58 STAB2 Zornitza Stark Classified gene: STAB2 as Red List (low evidence)
Bleeding and Platelet Disorders v1.58 STAB2 Zornitza Stark Gene: stab2 has been classified as Red List (Low Evidence).
Bleeding and Platelet Disorders v1.57 STAB2 Lucy Spencer gene: STAB2 was added
gene: STAB2 was added to Bleeding and Platelet Disorders. Sources: Literature
Mode of inheritance for gene: STAB2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: STAB2 were set to 40726512
Phenotypes for gene: STAB2 were set to Chronic thromboembolic pulmonary hypertension MONDO:0013024, STAB2-related
Review for gene: STAB2 was set to RED
Added comment: PMID: 40726512 In a cohort of chronic thromboembolic pulmonary hypertension a missense in STAB2 was found in 2 related affected individuals. However, the variant Ala1665Thr is common on gnomad with over 1000 hets and 4 homs. They also observed a significantly higher prevalence of 'qualifying alleles' in STAB2 in their disease cohort compared to the UK biobank- 4.6% in the disease cohort vs 1.2% in UK biobank. Qualifying alleles were rare and predicted deleterious. 78% of these variants were missense and quite a few of them also had thousands of hets and some homs in gnomad v4.
Sources: Literature