Pmm2 - Phosphomannomutase type 2
Predicted to enable phosphomannomutase activity. Involved in cellular response to hypoxia and protein N-linked glycosylation. Predicted to be active in cytosol. Is expressed in adult head. Used to study congenital disorder of glycosylation type I. Human ortholog(s) of this gene implicated in congenital disorder of glycosylation and congenital disorder of glycosylation Ia. Orthologous to human PMM1 (phosphomannomutase 1) and PMM2 (phosphomannomutase 2). [provided by Alliance of Genome Resources, Nov 2024]
NCBI Orthologs
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Protein alignment
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