The following gene names and symbols are associated with antigen Epilepsy, Progressive Myoclonus Type 2A, Lafora Disease (Laforin) across different species:

epilepsy, progressive myoclonus type 2A, Lafora disease (laforin) (EPM2A), laforin (LOC100355207)

Other aliases include:

EPM2, MELF

On the protein level the following designations are being used for antigen Epilepsy, Progressive Myoclonus Type 2A, Lafora Disease (Laforin):

laforin – epilepsy, progressive myoclonus type 2, Lafora disease (laforin)

Epilepsy, Progressive Myoclonus Type 2A, Lafora Disease (Laforin) fulfills a number of functions:

carbohydrate binding – hydrolase activity – protein binding – protein serine/threonine phosphatase activity – protein tyrosine phosphatase activity – protein tyrosine/serine/threonine phosphatase activity

Epilepsy, Progressive Myoclonus Type 2A, Lafora Disease (Laforin) is relevant to the following processes:

carbohydrate metabolic process – glycogen metabolic process – protein amino acid dephosphorylation

Locations for Epilepsy, Progressive Myoclonus Type 2A, Lafora Disease (Laforin):

cytoplasm – cytosol – endoplasmic reticulum – nucleus – plasma membrane – polysome

Source: NCBI Entrez Gene, Gene Ontology