nuclear factor 1 X-type isoform X3 [Homo sapiens]

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A rare cause of intellectual disability: Novel mutations of NFIX gene in two patients with clinical features of Marshall-Smith syndrome and Malan syndrome. [Int J Dev Neurosci. 2023]
A rare cause of intellectual disability: Novel mutations of NFIX gene in two patients with clinical features of Marshall-Smith syndrome and Malan syndrome.
Uzman CY, Gürsoy S, Hazan F. Int J Dev Neurosci. 2023 Aug; 83(5):479-485. Epub 2023 Jun 19.
NFIXing Cancer: The Role of NFIX in Oxidative Stress Response and Cell Fate. [Int J Mol Sci. 2023]
NFIXing Cancer: The Role of NFIX in Oxidative Stress Response and Cell Fate.
Ribeiro V, Martins SG, Lopes AS, Thorsteinsdóttir S, Zilhão R, Carlos AR. Int J Mol Sci. 2023 Feb 21; 24(5). Epub 2023 Feb 21.
CircNFIX stimulates the proliferation, invasion, and stemness properties of ovarian cancer cells by enhancing SH3RF3 mRNA stability via binding LIN28B. [Kaohsiung J Med Sci. 2023]
CircNFIX stimulates the proliferation, invasion, and stemness properties of ovarian cancer cells by enhancing SH3RF3 mRNA stability via binding LIN28B.
Yu XZ, Yang BW, Ao MY, Wu YK, Ye H, Wang RY, Xi MR, Hou MM. Kaohsiung J Med Sci. 2023 Mar; 39(3):234-243. Epub 2022 Dec 10.

RefSeq genomic sequence
See the genomic reference sequence for the NFIX gene (NG_032925.2).
RefSeq mRNA
See reference mRNA sequence for the NFIX gene (XM_054321074.1).
RefSeq protein isoforms
See 18 reference sequence protein isoforms for the NFIX gene.

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Protein