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| COVID-19 research v0.171 | SEC61A1 | Sophie Hambleton reviewed gene: SEC61A1: Rating: GREEN; Mode of pathogenicity: None; Publications: 28782633, 32325141; Phenotypes: Hypogammaglobulinaemia, recurrent infections, plasma cell deficiency, severe congenital neutropenia, tubulointerstitial and Glomerulocystic Kidney Disease with Anemia; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| COVID-19 research v0.40 | SEC61A1 |
Ellen McDonagh Source Expert Review Green was added to SEC61A1. Added phenotypes Severe recurrent respiratory tract infections; Predominantly Antibody Deficiencies; Hyperuricemic nephropathy, familial juvenile, 4, 617056; SEC61A1 deficiency for gene: SEC61A1 Rating Changed from Red List (low evidence) to Green List (high evidence) |
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| COVID-19 research v0.36 | SEC61A1 |
Ellen McDonagh gene: SEC61A1 was added gene: SEC61A1 was added to Viral susceptibility. Sources: IUIS Classification December 2019 Mode of inheritance for gene: SEC61A1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: SEC61A1 were set to 28782633; 32086639; 32048120 Phenotypes for gene: SEC61A1 were set to Severe recurrent respiratory tract infections; Predominantly Antibody Deficiencies; Hyperuricemic nephropathy, familial juvenile, 4, 617056; SEC61A1 deficiency |
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