Entrez 5238 | Ensembl ENSG00000013375 | |
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Aliases PGM3, AGM1, IMD23, PAGM, PGM 3, Phosphoglucomutase 3 External IDs MGI: 97566 HomoloGene: 9205 GeneCards: PGM3 |
Clinical significance
Mutations in PGM3 are associated to congenital disorder of glycosylation .
References
Phosphoglucomutase 3 Wikipedia(Text) CC BY-SA