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| Vitamin metabolism disorders v2.0 | SLC25A32 | Gene migrated from ENSG00000164933 to ENSG00000164933 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Vitamin metabolism disorders v1.2 | SLC25A32 |
Bryony Thompson gene: SLC25A32 was added gene: SLC25A32 was added to Vitamin metabolism disorders. Sources: Expert Review Green Mode of inheritance for gene: SLC25A32 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: SLC25A32 were set to 26933868; 28443623 Phenotypes for gene: SLC25A32 were set to Exercise intolerance, riboflavin-responsive, MONDO:0014795; Disorders of riboflavin metabolism |
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