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| Predominantly Antibody Deficiency v0.114 | POU2AF1 | Zornitza Stark Marked gene: POU2AF1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Predominantly Antibody Deficiency v0.114 | POU2AF1 | Zornitza Stark Gene: pou2af1 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Predominantly Antibody Deficiency v0.114 | POU2AF1 | Zornitza Stark Phenotypes for gene: POU2AF1 were changed from Agammaglobulinaemia to Agammaglobulinaemia, MONDO:0015977, POU2AF1-related | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Predominantly Antibody Deficiency v0.113 | POU2AF1 | Zornitza Stark Classified gene: POU2AF1 as Red List (low evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Predominantly Antibody Deficiency v0.113 | POU2AF1 | Zornitza Stark Gene: pou2af1 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Predominantly Antibody Deficiency v0.110 | POU2AF1 |
Peter McNaughton gene: POU2AF1 was added gene: POU2AF1 was added to Predominantly Antibody Deficiency. Sources: Literature Mode of inheritance for gene: POU2AF1 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: POU2AF1 were set to PMID: 33571536 Phenotypes for gene: POU2AF1 were set to Agammaglobulinaemia Review for gene: POU2AF1 was set to RED Added comment: Single patient from consanguineous parents lacking immunoglobulins despite normal total B-cell numbers. Sources: Literature |
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