Activity
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3 actions
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| Likely inborn error of metabolism v1.47 | MGAT2 |
Ivone Leong Source NHS GMS was added to MGAT2. Source London North GLH was added to MGAT2. |
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| Likely inborn error of metabolism v0.4 | MGAT2 |
Ellen McDonagh Added phenotypes N-acetylglucosaminyltransferase deficiency (Disorders of protein N-glycosylation); Congenital disorder of glycosylation, type IIa 212066 for gene: MGAT2 Publications for gene MGAT2 were changed from 27604308 to 19419693 |
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| Likely inborn error of metabolism v0.4 | MGAT2 |
Ellen McDonagh gene: MGAT2 was added gene: MGAT2 was added to Inborn errors of metabolism. Sources: Expert Review Green Mode of inheritance for gene: MGAT2 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: MGAT2 were set to 27604308 Phenotypes for gene: MGAT2 were set to N-acetylglucosaminyltransferase deficiency (Disorders of protein N-glycosylation); Congenital disorder of glycosylation, type IIa 212066 |
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