- accession:NM_014146
- 基因别名:LAT2
- 基因描述:Homo sapiens linker for activation of T cells family, member 2 (LAT2), transcript variant 3, mRNA.
- 载体:现货载体
- CDS区长度:732
- 翻译后氨基酸长度:243
- TranscriptVariant:This variant (3) differs in the 5' UTR compared to variant 1. All three variants encode the same protein.
- 基因简介:This gene is one of the contiguous genes at 7q11.23 commonly deleted in Williams syndrome, a multisystem developmental disorder. This gene consists of at least 14 exons, and its alternative splicing generates 3 transcript variants, all encoding the same protein. [provided by RefSeq, Jul 2008]
- 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