https://wikimd.com/index.php?action=history&feed=atom&title=MNX1 MNX1 - Revision history 2026-04-21T21:16:44Z Revision history for this page on the wiki MediaWiki 1.44.2 https://wikimd.com/index.php?title=MNX1&diff=6512811&oldid=prev Prab: CSV import 2025-03-17T18:08:09Z <p>CSV import</p> <table style="background-color: #fff; color: #202122;" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr class="diff-title" lang="en"> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 18:08, 17 March 2025</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l32">Line 32:</td> <td colspan="2" class="diff-lineno">Line 32:</td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; 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font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">__NOINDEX__</ins></div></td></tr> </table> Prab https://wikimd.com/index.php?title=MNX1&diff=6265694&oldid=prev Prab: CSV import 2025-02-11T00:23:50Z <p>CSV import</p> <table style="background-color: #fff; color: #202122;" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr class="diff-title" lang="en"> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 00:23, 11 February 2025</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l31">Line 31:</td> <td colspan="2" class="diff-lineno">Line 31:</td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>[[Category:Endocrine system]]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>[[Category:Endocrine system]]</div></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{{gene-stub}}</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{{gene-stub}}</div></td></tr> <tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">{{No image}}</ins></div></td></tr> </table> Prab https://wikimd.com/index.php?title=MNX1&diff=5329007&oldid=prev Prab: CSV import 2024-02-29T02:45:50Z <p>CSV import</p> <p><b>New page</b></p><div>&#039;&#039;&#039;MNX1&#039;&#039;&#039; (also known as &#039;&#039;&#039;Motor Neuron and Pancreas Homeobox 1&#039;&#039;&#039;) is a [[gene]] that encodes a [[protein]] playing a crucial role in the development of the [[pancreas]] and the [[motor neuron]]s. Mutations in this gene are associated with several disorders, including [[Currarino syndrome]] and [[congenital hypopituitarism]].<br /> <br /> == Function ==<br /> <br /> The MNX1 gene provides instructions for making a protein that is involved in the development of motor neurons and the pancreas. This protein is a [[transcription factor]], which means it attaches (binds) to specific regions of [[DNA]] and helps control the activity of particular genes.<br /> <br /> == Clinical significance ==<br /> <br /> Mutations in the MNX1 gene can lead to several disorders. The most common is Currarino syndrome, a condition characterized by a triad of anomalies: a sacral defect, anorectal malformation, and a presacral mass. <br /> <br /> Another disorder associated with mutations in the MNX1 gene is congenital hypopituitarism, a condition that affects the [[pituitary gland]] and can lead to growth failure, delayed puberty, and other health problems.<br /> <br /> == See also ==<br /> <br /> * [[Gene]]<br /> * [[Protein]]<br /> * [[Transcription factor]]<br /> * [[DNA]]<br /> * [[Currarino syndrome]]<br /> * [[Congenital hypopituitarism]]<br /> <br /> == References ==<br /> <br /> {{reflist}}<br /> <br /> [[Category:Genes]]<br /> [[Category:Proteins]]<br /> [[Category:Transcription factors]]<br /> [[Category:DNA]]<br /> [[Category:Genetic disorders]]<br /> [[Category:Endocrine system]]<br /> {{gene-stub}}</div> Prab