7qqe
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Nuclear factor one X - NFIX in P41212
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Structural highlights
DiseaseNFIX_HUMAN Marshall-Smith syndrome;Malan overgrowth syndrome;19p13.3 microduplication syndrome. The disease is caused by variants affecting the gene represented in this entry. The disease is caused by variants affecting the gene represented in this entry. FunctionNFIX_HUMAN Recognizes and binds the palindromic sequence 5'-TTGGCNNNNNGCCAA-3' present in viral and cellular promoters and in the origin of replication of adenovirus type 2. These proteins are individually capable of activating transcription and replication. Contents | ||||||||||||||||||||
This page was last modified 05:37, 24 December 2025.