<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">kcnj16</th>
</tr>
<tr>
<td class="label">Species</td>
<td>Kir5.1 Homolog</td>
</tr>
<tr>
<td class="label">D. rerio</td>
<td>kcnj16</td>
</tr>
<tr>
<td class="label">G. gallus</td>
<td>KCNJ16</td>
</tr>
<tr>
<td class="label">M. musculus</td>
<td>Kcnj16</td>
</tr>
<tr>
<td class="label">R. norvegicus</td>
<td>Kcnj16</td>
</tr>
<tr>
<td class="label">*H.
<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">kcnj16</th>
</tr>
<tr>
<td class="label">Species</td>
<td>Kir5.1 Homolog</td>
</tr>
<tr>
<td class="label">D. rerio</td>
<td>kcnj16</td>
</tr>
<tr>
<td class="label">G. gallus</td>
<td>KCNJ16</td>
</tr>
<tr>
<td class="label">M. musculus</td>
<td>Kcnj16</td>
</tr>
<tr>
<td class="label">R. norvegicus</td>
<td>Kcnj16</td>
</tr>
<tr>
<td class="label">H. sapiens</td>
<td>KCNJ16</td>
</tr>
<tr>
<td class="label">Brain Region</td>
<td>Expression</td>
</tr>
<tr>
<td class="label">Hippocampus</td>
<td>High</td>
</tr>
<tr>
<td class="label">Cerebellum</td>
<td>High</td>
</tr>
<tr>
<td class="label">Cortex</td>
<td>Moderate</td>
</tr>
<tr>
<td class="label">Basal ganglia</td>
<td>Moderate</td>
</tr>
<tr>
<td class="label">Substantia nigra</td>
<td>Moderate</td>
</tr>
<tr>
<td class="label">Gene Symbol</td>
<td>KCNJ16</td>
</tr>
<tr>
<td class="label">Full Name</td>
<td>Potassium Inwardly Rectifying Channel Subfamily J Member 16</td>
</tr>
<tr>
<td class="label">Chromosomal Location</td>
<td>17q24.3</td>
</tr>
<tr>
<td class="label">NCBI Gene ID</td>
<td>3773</td>
</tr>
<tr>
<td class="label">Ensembl ID</td>
<td>ENSG00000186891</td>
</tr>
<tr>
<td class="label">UniProt ID</td>
<td>Q9NP82</td>
</tr>
<tr>
<td class="label">OMIM</td>
<td>613228</td>
</tr>
<tr>
<td class="label">Gene Type</td>
<td>Protein coding</td>
</tr>
<tr>
<td class="label">Protein Name</td>
<td>Kir5.1 (inward rectifier K+ channel 5.1)</td>
</tr>
<tr>
<td class="label">Molecular Weight</td>
<td>48 kDa</td>
</tr>
<tr>
<td class="label">Amino Acids</td>
<td>427</td>
</tr>
<tr>
<td class="label">Subcellular Localization</td>
<td>Plasma membrane</td>
</tr>
<tr>
<td class="label">Channel Family</td>
<td>Kir (inwardly rectifying potassium)</td>
</tr>
<tr>
<td class="label">Single-channel conductance</td>
<td>30 pS</td>
</tr>
<tr>
<td class="label">Inward rectification</td>
<td>Strong</td>
</tr>
<tr>
<td class="label">pH sensitivity</td>
<td>pKa ~ 7.0</td>
</tr>
<tr>
<td class="label">PIP2 requirement</td>
<td>High</td>
</tr>
<tr>
<td class="label">Combination</td>
<td>Properties</td>
</tr>
<tr>
<td class="label">Kir5.1/Kir4.1</td>
<td>pH-sensitive, brain-expressed</td>
</tr>
<tr>
<td class="label">Kir5.1/Kir4.1 (renal)</td>
<td>pH-sensitive, kidney-expressed</td>
</tr>
<tr>
<td class="label">Kir5.1 homomeric</td>
<td>Less common</td>
</tr>
<tr>
<td class="label">Domain</td>
<td>Residues</td>
</tr>
<tr>
<td class="label">N-terminus</td>
<td>1-70</td>
</tr>
<tr>
<td class="label">Transmembrane 1</td>
<td>71-95</td>
</tr>
<tr>
<td class="label">Pore loop</td>
<td>140-170</td>
</tr>
<tr>
<td class="label">Transmembrane 2</td>
<td>195-220</td>
</tr>
<tr>
<td class="label">C-terminus</td>
<td>221-427</td>
</tr>
<tr>
<td class="label">Variant</td>
<td>Effect</td>
</tr>
<tr>
<td class="label">rs12926049</td>
<td>Promoter</td>
</tr>
<tr>
<td class="label">rs2273604</td>
<td>Non-coding</td>
</tr>
<tr>
<td class="label">c. 514G>A</td>
<td>Missense</td>
</tr>
<tr>
<td class="label">Approach</td>
<td>Agent</td>
</tr>
<tr>
<td class="label">Channel openers</td>
<td>Retigabine</td>
</tr>
<tr>
<td class="label">Gene therapy</td>
<td>AAV-KCNJ16</td>
</tr>
<tr>
<td class="label">pH modulators</td>
<td>Small molecules</td>
</tr>
<tr>
<td class="label">Protein</td>
<td>Interaction</td>
</tr>
<tr>
<td class="label">KCNJ10</td>
<td>Heteromer</td>
</tr>
<tr>
<td class="label">PIP2</td>
<td>Cofactor</td>
</tr>
<tr>
<td class="label">Intracellular pH</td>
<td>Modulator</td>
</tr>
<tr>
<td class="label">ATP</td>
<td>Modulator</td>
</tr>
<tr>
<td class="label">Biomarker</td>
<td>Disease</td>
</tr>
<tr>
<td class="label">KCNJ16 expression</td>
<td>AD</td>
</tr>
<tr>
<td class="label">KCNJ16 expression</td>
<td>PD</td>
</tr>
<tr>
<td class="label">Kir5.1 current</td>
<td>AD</td>
</tr>
<tr>
<td class="label">KG Connections</td>
<td><a href="/atlas" style="color:#4fc3f7">1 edges</a></td>
</tr>
</table>
KCNJ16 (Potassium Inwardly Rectifying Channel Subfamily J Member 16) encodes Kir5.1, an inwardly rectifying potassium (K+) channel that plays critical roles in neuronal and renal function[@inwardly2010]. Kir5.1 (encoded by KCNJ16) typically forms heteromeric channels with Kir4.1 (encoded by [KCNJ10](/genes/kcnj10)) to create pH-sensitive K+ channels important for maintaining neuronal resting membrane potential, potassium homeostasis, and cellular pH regulation. Genetic variants in KCNJ16 have been associated with altered risk for Alzheimer's disease[@kcnj2019].
The KCNJ16 gene is located on chromosome 17q24.3 and encodes a 427-amino acid protein. Kir5.1 channels conduct K+ ions preferentially in the inward direction (into the cell), helping to maintain the negative resting membrane potential essential for neuronal excitability. The channel is highly sensitive to intracellular pH, with activity increasing under acidic conditions to help regulate cellular pH homeostasis[@yuan2017].
Kir channels are conserved across species:
Kir5.1 channels exhibit[@pip2005]:
Kir5.1 primarily forms heteromeric channels with Kir4.1:
Kir5.1 dysfunction may contribute to AD through[@patel2018]:
In PD, Kir channels play roles in[@schram2019]:
K+ channel dysfunction contributes to epilepsy[@potassium2012]: