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| Severe Combined Immunodeficiency v2.0 | RAG2 | Gene migrated from ENSG00000175097 to ENSG00000175097 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Severe Combined Immunodeficiency v1.24 | Bryony Thompson Copied gene RAG2 from panel Severe Combined Immunodeficiency (absent T absent B cells) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Severe Combined Immunodeficiency v1.24 | RAG2 |
Bryony Thompson gene: RAG2 was added gene: RAG2 was added to Severe Combined Immunodeficiency (absent T present B cells). Sources: Expert Review Green,Melbourne Genomics Health Alliance Immunology Flagship,Victorian Clinical Genetics Services Mode of inheritance for gene: RAG2 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: RAG2 were set to 26996199 Phenotypes for gene: RAG2 were set to Recombinase activating gene 2 deficiency MONDO:0000573 |
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