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| Phagocyte Defects v2.0 | DBF4 | Gene migrated from ENSG00000006634 to ENSG00000006634 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Phagocyte Defects v1.32 | DBF4 | Bryony Thompson Marked gene: DBF4 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Phagocyte Defects v1.32 | DBF4 | Bryony Thompson Gene: dbf4 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Phagocyte Defects v1.32 | DBF4 |
Bryony Thompson gene: DBF4 was added gene: DBF4 was added to Phagocyte Defects. Sources: Expert list Mode of inheritance for gene: DBF4 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: DBF4 were set to 36841265 Phenotypes for gene: DBF4 were set to severe congenital neutropenia MONDO:0018542 Review for gene: DBF4 was set to RED Added comment: A single case with a homozygous variant & some supporting in vitro functional assay. Sources: Expert list |
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