甲状腺激素α受体

甲状腺激素α受体(THR-α,TR-α),也称:核受体家族1, A组, 成员1 (NR1A1),是一类核受体蛋白,在人类中由THR-α基因编码。[7][8][9]

甲状腺激素α受体
已知的結構
PDB直系同源搜索: PDBe RCSB
識別號
别名THRA;, AR7, CHNG6, EAR7, ERB-T-1, ERBA, ERBA1, NR1A1, THRA1, THRA2, c-ERBA-1, thyroid hormone receptor, alpha, thyroid hormone receptor alpha, TRalpha
外部IDOMIM190120 MGI98742 HomoloGene37747 GeneCardsTHRA
相關疾病
congenital nongoitrous hypothryoidism 6[1]
為以下藥物的標靶
反三碘甲状腺原氨酸替拉曲可三碘甲腺原氨酸左旋甲狀腺素鈉[2]
基因位置(人类
17號染色體
染色体17號染色體[3]
17號染色體
甲状腺激素α受体的基因位置
甲状腺激素α受体的基因位置
基因座17q21.1起始40,058,290 bp[3]
终止40,093,867 bp[3]
RNA表达模式


查阅更多表达数据
直系同源
物種人類小鼠
Entrez

7067

21833

Ensembl

ENSG00000126351

ENSMUSG00000058756

UniProt

P10827

P63058

mRNA序列

NM_199334
​NM_001190918
​NM_001190919
​NM_003250

NM_178060
​NM_001313983

蛋白序列

NP_001177847
​NP_001177848
​NP_003241
​NP_955366

NP_001300912
​NP_835161

基因位置(UCSC)Chr 17: 40.06 – 40.09 MbChr 11: 98.63 – 98.66 Mb
PubMed查找[5][6]
維基數據

功能

该基因编码的蛋白质为三碘甲腺原氨酸的核激素受体。它是甲状腺激素多种受体之一,已被证明可以调节甲状腺激素的生物活性, 小鼠敲除实验表明不同的受体虽然具有一定程度的冗余,但可能介导甲状腺激素的不同功能。[7]

病理学作用

THRA基因突变可能导致甲状腺功能减退症, 一种先天性甲状腺机能低下症亚型。

基因相互作用

甲状腺激素受体 α 已被证明与以下存在基因相互作用

参考文献

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  3. GRCh38: Ensembl release 89: ENSG00000126351 - Ensembl, May 2017
  4. GRCm38: Ensembl release 89: ENSMUSG00000058756 - Ensembl, May 2017
  5. . National Center for Biotechnology Information, U.S. National Library of Medicine.
  6. . National Center for Biotechnology Information, U.S. National Library of Medicine.
  7. .
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