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- accession：NM_001166135
- 基因别名：RBM28
- 基因描述：Homo sapiens RNA binding motif protein 28 (RBM28), transcript variant 2, mRNA.
- 载体：现货载体
- CDS区长度：1857
- 翻译后氨基酸长度：618
- TranscriptVariant：This variant (2) lacks four exons in the 5' coding region, as compared to variant 1. The reading frame is not changed, but the resulting isoform (2) has lost part of the RRMs 1 and 2, as compared to isoform 1.
- 基因简介：The protein encoded by this gene is a specific nucleolar component of the spliceosomal small nuclear ribonucleoprotein (snRNP)complexes . It specifically associates with U1, U2, U4, U5, and U6 small nuclear RNAs (snRNAs), possibly coordinating their transition through the nucleolus. Mutation in this gene causes alopecia, progressive neurological defects, and endocrinopathy (ANE syndrome), a pleiotropic and clinically heterogeneous disorder. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 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
