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- accession：NM_001146040
- 基因别名：GLRA1
- 基因描述：Homo sapiens glycine receptor, alpha 1 (GLRA1), transcript variant 1, mRNA.
- 载体：现货载体
- CDS区长度：1374
- 翻译后氨基酸长度：457
- TranscriptVariant：This variant (1) represents the longer transcript and encodes the longer isoform (1).
- 基因简介：The protein encoded by this gene is a subunit of a pentameric inhibitory glycine receptor. The receptor mediates postsynaptic inhibition in the central nervous system. Defects in this gene are a cause of startle disease (STHE), also known as hereditary hyperekplexia or congenital stiff-person syndrome. Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2009]
- 规格：10ul 质粒
CDS区参考序列： 点击查看序列翻译后氨基酸参数序列： 点击查看序列
