SLC6A19 Gene - GeneCards | S6A19 Protein | S6A19 Antibody
2016年12月25日 · SLC6A19 (Solute Carrier Family 6 Member 19) is a Protein Coding gene. Diseases associated with SLC6A19 include Hartnup Disorder and Iminoglycinuria. Among its …
Molecular basis of inhibition of the amino acid transporter B
2024年8月22日 · The epithelial neutral amino acid transporter B 0 AT1 (SLC6A19) is the major transporter for the absorption of neutral amino acids in the intestine and their reabsorption in...
溶质载体家族 6 成员 19（SLC6A19）基因 | MCE
B0AT1 (SLC6A19) 在肠细胞中的表达和功能取决于辅助蛋白血管紧张素转换酶 2 (ACE2) 的存在，其除其他功能外，还充当 B0AT1 膜运输的伴侣。 ACE2 还是严重急性呼吸系统综合症冠状 …
抑制氨基酸转运蛋白 B0AT1 的分子基础 （SLC6A19）,Nature …
上皮中性氨基酸转运蛋白 b0at1 （slc6a19） 是中性氨基酸在肠道中吸收及其在肾脏中重吸收的主要转运蛋白。 小鼠模型已经证明，缺乏 B0AT1 可以使罕见氨基酸代谢紊乱（如苯丙酮尿症和 …
SLC6A19 | 人类基因组 | 生物系统数据库 - biosysdb.com
This gene encodes a system B (0) transmembrane protein that actively transports most neutral amino acids across the apical membrane of epithelial cells. Mutations in this gene may result …
Sodium-dependent neutral amino acid transporter B(0)AT1
Sodium-dependent neutral amino acid transporter B (0)AT1 is a protein that in humans is encoded by the SLC6A19 gene. [5] SLC6A19 is a system B (0) transporter that mediates epithelial …
科研动态｜南方科技大学医学院鄢仁鸿/王子龙团队合作解析SLC6 …
B0AT1 (SLC6A19)和 SIT1 (SLC6A20)是 SLC6 家族的重要成员，它们通过与血管紧张素转换酶2 (ACE2) 结合定位到细胞膜上共同行使底物转运功能。 ACE2蛋白是一种调节血管紧张素 (Ang) …
SLC6A19 solute carrier family 6 member 19 [ (human)]
2025年2月8日 · We identified six mutations in SLC6A19 that cosegregated with disease in the predicted recessive manner, with most affected individuals being compound heterozygotes. …
SLC6A19 - 药物、适应症、专利 - 智慧芽新药情报库
slc6a19 是研究中一个关键验证的基因。这一基因编码一种氨基酸转运蛋白，主要负责肾脏和小肠中氨基酸的吸收。研究发现，slc6a19 的罕见变异不仅与氨基酸代谢物水平相关，还可能影响 …
The role of the neutral amino acid transporter B0AT1 (SLC6A19) …
The disorder is caused by mutations in the neutral amino acid transporter B(0)AT1 (SLC6A19). To date 21 mutations have been identified in more than twenty families. SLC6A19 requires either …