Gene EPM2A function profile ��Ʈw

Gene Symbol

Gene Name	Aliases	Previous_Symbol
EPM2A	epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)	LDE, LD	epilepsy, progressive myoclonus type 2, Lafora disease (laforin)

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MeSH term

Frequency	Condition_Probility
Amino Acid Sequence	8	0.0
Animals	7	0.0
COS Cells	3	0.0
Cell Line	2	0.0
Gene Library	3	0.0
Humans	16	0.0
Molecular Sequence Data	11	0.0
Mutation	4	0.0
Protein Structure, Tertiary	2	0.0
Protein-Tyrosine-Phosphatase/chemistry/*genetics	2	25.0
Research Support, Non-U.S. Gov't	11	0.0
Research Support, U.S. Gov't, P.H.S.	3	0.0
Transfection	2	0.0
Adolescent	3	0.0
Adult	4	0.0
Base Sequence	5	0.0
Child	4	0.0
Female	5	0.0
Genotype	2	0.0
Haplotypes	2	0.0
In Situ Hybridization, Fluorescence	3	0.0
Infant	2	0.0
Lafora Disease/*genetics	3	100.0
Male	5	0.0
Protein-Tyrosine-Phosphatase/*genetics	3	2.0
Conserved Sequence	2	0.0
Mice	5	0.0
Mutation, Missense	2	0.0
*Phylogeny	2	1.0
Sequence Alignment	2	0.0
Sequence Homology, Amino Acid	5	0.0
Lafora Disease/genetics	2	66.0
DNA Mutational Analysis	3	0.0
Genes, Recessive	3	0.0
Linkage (Genetics)	2	0.0
Microsatellite Repeats	2	0.0
Pedigree	4	0.0
Cloning, Molecular	2	0.0
Hela Cells	2	0.0
Protein Binding	2	0.0
Glucans/metabolism	2	50.0
*Mutation	2	0.0
RNA, Messenger/metabolism	2	0.0
Mice, Knockout	2	0.0
Recombinant Fusion Proteins/metabolism	2	0.0
Two-Hybrid System Techniques	2	0.0