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- accession：NM_148913
- 基因别名：ABHD11
- 基因描述：Homo sapiens abhydrolase domain containing 11 (ABHD11), transcript variant 2, mRNA.
- 载体：现货载体
- CDS区长度：927
- 翻译后氨基酸长度：308
- TranscriptVariant：This variant (2) lacks an alternate in-frame segment, compared to variant 1, resulting in a shorter isoform (2), also known as form D, which shares N- and C-termini with isoform 1.
- 基因简介：This gene encodes a protein containing an alpha/beta hydrolase fold domain. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [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
