1. Gene
  2. Epm2a - EPM2A glucan phosphatase, laforin Gene

Epm2a - EPM2A glucan phosphatase, laforin Gene

Rattus norvegicus
Gene ID: 114005 | Gene type: protein coding

About Epm2a

Summary

Predicted to enable several functions, including glycogen (starch) synthase activity; Phosphatase activity; and polysaccharide binding activity. Predicted to be involved in several processes, including carbohydrate phosphorylation; dephosphorylation; and glycogen metabolic process. Predicted to act upstream of or within several processes, including glycogen biosynthetic process; habituation; and regulation of cellular protein metabolic process. Predicted to be located in several cellular components, including cytoplasmic side of rough endoplasmic reticulum membrane; dendrite; and perikaryon. Predicted to be part of polysome. Predicted to be active in cytoplasm and nucleus. Human ortholog(s) of this gene implicated in Lafora disease and progressive myoclonus epilepsy. Orthologous to human EPM2A (EPM2A glucan Phosphatase, laforin). [provided by Alliance of Genome Resources, Apr 2022]

Epm2a Products(1)

mRNA Protein Name
NM_001276762.1 NP_001263691.1 laforin
Protein Preferred Names Protein Names

laforin

EPM2A, laforin glucan phosphatase

LAFPTPase

epilepsy, progressive myoclonic epilepsy, type 2 gene alpha

epilepsy, progressive myoclonus type 2A

glucan phosphatase

lafora PTPase

Orthologs Information

Species Symbol Source ID
Homo sapiens Epm2a NCBI NCBI:7957