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| Proteinuria v0.169 | SPRY2 | Bryony Thompson Marked gene: SPRY2 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Proteinuria v0.169 | SPRY2 | Bryony Thompson Gene: spry2 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Proteinuria v0.169 | SPRY2 |
Bryony Thompson changed review comment from: A single family reported with expression analyses conducted in some patient cells. Sources: Literature; to: A single family reported with expression analyses conducted in some patient cells. No variants identified in 70 apparently sporadic cases with IgAN. Sources: Literature |
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| Proteinuria v0.169 | SPRY2 |
Bryony Thompson gene: SPRY2 was added gene: SPRY2 was added to Proteinuria. Sources: Literature Mode of inheritance for gene: SPRY2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: SPRY2 were set to 25782674 Phenotypes for gene: SPRY2 were set to {?IgA nephropathy, susceptibility to, 3} MIM#616818 Review for gene: SPRY2 was set to RED Added comment: A single family reported with expression analyses conducted in some patient cells. Sources: Literature |
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