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EPM2AIP1

EPM2A (laforin) interacting protein 1

The EPM2A gene, which encodes laforin, is mutated in an autosomal recessive form of adolescent progressive myoclonus epilepsy. The protein encoded by this gene binds to laforin, but its function is not known. This gene is intronless.

Gene Name:	EPM2A (laforin) interacting protein 1
Synonyms:	EPM2AIP1, EPM2A interacting protein 1, EPM2A-interacting protein 1, KIAA0766, Laforin-interacting protein
Target Sequences:	NM_014805 NP_055620.1 Q7L775

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For RESEARCH USE ONLY. Intended for use by laboratory professionals. Not intended for human diagnostic or therapeutic purposes.

The data on this page has been compiled from LifeSpan internal sources, the National Center for Biotechnology Information (NCBI), and The Universal Protein Resource (UniProt).

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