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WNT9A — Wnt Family Member 9A

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gene1206 wordssynced 2026-04-02

WNT9A — Wnt Family Member 9A

Overview

<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">WNT9A — Wnt Family Member 9A</th>
</tr>
<tr>
<td class="label">Symbol</td>
<td><strong>WNT9A</strong></td>
</tr>
<tr>
<td class="label">Full Name</td>
<td>WNT9A — Wnt Family Member 9A</td>
</tr>
<tr>
<td class="label">Type</td>
<td>Gene</td>
</tr>
<tr>
<td class="label">NCBI</td>
<td><a href="https://www.ncbi.nlm.nih.gov/gene/?term=WNT9A" target="_blank">Search NCBI</a></td>
</tr>
<tr>
<td class="label">KG Connections</td>
<td><a href="/atlas" style="color:#4fc3f7">1 edges</a></td>
</tr>
</table>

WNT9A (Wnt Family Member 9A) is a secreted signaling protein belonging to the Wnt family that plays essential roles in embryonic development, tissue patterning, and adult tissue homeostasis[@wntfamily2023]. Like other Wnt proteins, WNT9A activates canonical Wnt/β-catenin signaling by binding to Frizzled receptors and LRP co-receptors, leading to β-catenin stabilization and translocation to the nucleus where it activates TCF/LEF target genes[@wntneuro2022].

WNT9A is particularly important for kidney development (nephrogenesis) and has been implicated in neural progenitor cell regulation, synaptic function, and cancer progression[@wnt9adev2018]. Altered WNT9A signaling has been reported in Alzheimer's disease and other neurodegenerative conditions, where Wnt pathway dysregulation contributes to disease pathogenesis[@wntbeta2021].

Molecular Biology

Gene and Protein Structure


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