EPM2AIP1 抗体
(EPM2A (Laforin) Interacting Protein 1 (EPM2AIP1))
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. [provided by RefSeq, Oct 2008].
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Latest Publications for our EPM2AIP1 抗体
: "Deficiency of a glycogen synthase-associated protein, Epm2aip1, causes decreased glycogen synthesis and hepatic insulin resistance." in: The Journal of biological chemistry, Vol. 288, Issue 48, pp. 34627-37, (2013) (PubMed).: "Identification of a novel protein interacting with laforin, the EPM2a progressive myoclonus epilepsy gene product." in: Genomics, Vol. 81, Issue 6, pp. 579-87, (2003) (PubMed).
: "Prediction of the coding sequences of unidentified human genes. XI. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro." in: DNA research : an international journal for rapid publication of reports on genes and genomes, Vol. 5, Issue 5, pp. 277-86, (1999) (PubMed).
Aliases for EPM2AIP1 抗体
EPM2A interacting protein 1 (EPM2AIP1) 抗体EPM2A (laforin) interacting protein 1 (EPM2AIP1) 抗体
EPM2A interacting protein 1 (Epm2aip1) 抗体
EPM2A (laforin) interacting protein 1 (Epm2aip1) 抗体
A930003G21Rik 抗体
DKFZp459D2251 抗体
EPM2AIP1 抗体
mKIAA0766 抗体
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