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- accession：NM_001168376
- 基因别名：DYX2; NMIG; DYLX2
- 基因描述：Homo sapiens KIAA0319 (KIAA0319), transcript variant 4, mRNA.
- 载体：现货载体
- CDS区长度：3084
- 翻译后氨基酸长度：1027
- TranscriptVariant：This variant (4) differs in the 5' UTR, lacks an exon and initiates translation at a downstream, in-frame start codon, compared to variant 1. The encoded isoform (c) has a shorter N-terminus, compared to isoform a.
- 基因简介：This gene encodes a transmembrane protein that contains a large extracellular domain with multiple polycystic kidney disease (PKD) domains. The encoded protein may play a role in the development of the cerebral cortex by regulating neuronal migration and cell adhesion. Single nucleotide polymorphisms in this gene are associated with dyslexia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]
- 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
