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From Proteopedia
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== Disease == | == Disease == | ||
| - | [https://www.uniprot.org/uniprot/NFIX_HUMAN NFIX_HUMAN] | + | [https://www.uniprot.org/uniprot/NFIX_HUMAN NFIX_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. |
== Function == | == Function == | ||
[https://www.uniprot.org/uniprot/NFIX_HUMAN NFIX_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. | [https://www.uniprot.org/uniprot/NFIX_HUMAN NFIX_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. | ||
Current revision
Nuclear factor one X - NFIX in P41212
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Categories: Homo sapiens | Large Structures | Bais G | Chaves-Sanjuan A | Demitri N | Gourlay LJ | Lapi M | Nardini M | Polentarutti M | Tiberi M
