| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Defects of intrinsic and innate immunity v1.29 | LY9 | Zornitza Stark Marked gene: LY9 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Defects of intrinsic and innate immunity v1.29 | LY9 | Zornitza Stark Gene: ly9 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Defects of intrinsic and innate immunity v1.29 | Zornitza Stark Copied gene LY9 from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Defects of intrinsic and innate immunity v1.29 | LY9 |
Zornitza Stark gene: LY9 was added gene: LY9 was added to Defects of intrinsic and innate immunity. Sources: Expert Review Green,Literature Mode of inheritance for gene: LY9 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: LY9 were set to 40446017 Phenotypes for gene: LY9 were set to Inborn error of immunity, MONDO:0003778, LY9-related |
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| Defects of intrinsic and innate immunity v0.168 | LY96 | Bryony Thompson Marked gene: LY96 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Defects of intrinsic and innate immunity v0.168 | LY96 | Bryony Thompson Gene: ly96 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Defects of intrinsic and innate immunity v0.168 | LY96 |
Bryony Thompson gene: LY96 was added gene: LY96 was added to Defects of innate immunity. Sources: Expert list Mode of inheritance for gene: LY96 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: LY96 were set to 36462957 Phenotypes for gene: LY96 were set to Inborn error of immunity, MONDO:0003778, LY96-related Review for gene: LY96 was set to RED Added comment: Only a single family reported. The IUIS IEI committee categorises this gene as TLR Signaling Pathway Deficiency. Sources: Expert list |
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