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- accession：NM_001130997
- 基因别名：FAM58A
- 基因描述：Homo sapiens family with sequence similarity 58, member A (FAM58A), transcript variant 2, mRNA.
- 载体：现货载体
- CDS区长度：687
- 翻译后氨基酸长度：228
- TranscriptVariant：This variant (2) differs in the 3' coding region, compared to variant 1, resulting in an isoform (2) with a region missing from the C-terminus, compared to isoform 1.
- 基因简介：Mutations in this gene have been shown to cause an X-linked dominant STAR syndrome that typically manifests syndactyly, telecanthus and anogenital and renal malformations. The protein encoded by this gene contains a cyclin-box-fold domain which suggests it may have a role in controlling nuclear cell division cycles. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 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
