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Immunogen sequence: HNSWSSSSRH PNQATPKKSG LKNGQMKNKD DECFGDDIEE IPDTDFDFEG NLALFDKAAV FEEIDTYERR SGTRSRGIPN ERPTRYRHDE NILESEPIVY RRIIVPHNVS KEFCTDSGLV VPSISYELHK KLLSVAEKHG LTLERRLEMT GVCASQMALT LLGGPNRLNP KNVHQRPTVA LLCGPHVKGA QGISCGRHLA NHDVQVILFL PNFVKMLESI TNELSLFSKT QGQQVSSLKD LPTSPVDLVI NCLDCPENVF LRDQPWYKAA VAWANQNRAP VLSIDPPVHE VEQGIDAKWS LALGLPLPLG EHAGRIYLCD IGIPQQVFQE VGINYHSPFG CKFVIPLHSA; Positive Samples: U-87MG, MCF-7, HeLa, Mouse pancreas; Cellular Location: Cytoplasm, P-body
This gene encodes a protein that is important in mRNA degradation. The encoded protein is a component of a decapping complex that promotes efficient removal of the monomethylguanosine (m7G) cap from mRNAs, as part of the 5' to 3' mRNA decay pathway. Mutations in this gene have been identified in human patients with an autosomal recessive form of intellectual disability.
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Protein Aliases: enhancer of mRNA decapping 3; enhancer of mRNA decapping 3 homolog; Enhancer of mRNA-decapping protein 3; hYjeF_N2; hYjeF_N2-15q23; LSM16 homolog; LSM16 homolog (EDC3, S. cerevisiae); yjeF domain containing; YjeF domain-containing protein 1; YjeF N-terminal domain-containing protein 2; YjeF_N2
Gene Aliases: AA517853; EDC3; LSM16; MRT50; PP844; RGD1306898; YJDC; YJEFN2
UniProt ID: (Human) Q96F86, (Mouse) Q8K2D3
Entrez Gene ID: (Human) 80153, (Rat) 315708, (Mouse) 353190
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