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Protein-coding gene in the species Homo sapiens
Nuclear fragile X mental retardation-interacting protein 2 is a protein that in humans is encoded by the NUFIP2 gene .[ 5] [ 6] [ 7]
NUFIP2 has been shown to interact with FMR1 and Roquin-1.[ 8] [ 5]
^ a b c GRCh38: Ensembl release 89: ENSG00000108256 – Ensembl , May 2017
^ a b c GRCm38: Ensembl release 89: ENSMUSG00000037857 – Ensembl , May 2017
^ "Human PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .
^ "Mouse PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .
^ a b Bardoni B, Castets M, Huot ME, Schenck A, Adinolfi S, Corbin F, Pastore A, Khandjian EW, Mandel JL (Jul 2003). "82-FIP, a novel FMRP (fragile X mental retardation protein) interacting protein, shows a cell cycle-dependent intracellular localization" . Hum Mol Genet . 12 (14): 1689– 98. doi :10.1093/hmg/ddg181 . PMID 12837692 .
^ Ramos A, Hollingworth D, Adinolfi S, Castets M, Kelly G, Frenkiel TA, Bardoni B, Pastore A (Jan 2006). "The structure of the N-terminal domain of the fragile X mental retardation protein: a platform for protein-protein interaction" . Structure . 14 (1): 21– 31. doi :10.1016/j.str.2005.09.018 . PMID 16407062 .
^ "Entrez Gene: NUFIP2 nuclear fragile X mental retardation protein interacting protein 2" .
^ Rehage N (2018). "Binding of NUFIP2 to Roquin promotes recognition and regulation of ICOS mRNA" . Nature Communications . 9 (1): 299. Bibcode :2018NatCo...9..299R . doi :10.1038/s41467-017-02582-1 . PMC 5775257 . PMID 29352114 .
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