This gene encodes a member of the inwardly rectifying potassium channel family. Transcription of this locus is regulated by thyroid hormone, and the encoded protein plays a role in resting membrane potential maintenance. Mutations in this locus have been associated with thyrotoxic hypokalemic periodic paralysis. [provided by RefSeq, Jan 2013]
人 KCNJ18 (NM_001194958) cDNA克隆
| Accession: | NM_001194958 |
|---|---|
| 基因名称: | KCNJ18 |
| 基因别名: | TTPP2; KIR2.6 |
| 基因描述: | Homo sapiens potassium inwardly-rectifying channel, subfamily J, member 18 (KCNJ18), mRNA. |
| 种属: | Human |
| CDS区长度: | 1302 (查看编码区序列) |
| 翻译后氨基酸长度: | 433 (查看氨基酸序列) |
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