• accession：NM_006304
• 基因别名：SHFM1
• 基因描述：Homo sapiens split hand/foot malformation (ectrodactyly) type 1 (SHFM1), mRNA.
• 载体：现货载体
• CDS区长度：213
• 翻译后氨基酸长度：70
• 基因简介：The product of this gene has been localized within the split hand/split foot malformation locus SHFM1 at chromosome 7. It has been proposed to be a candidate gene for the autosomal dominant form of the heterogeneous limb developmental disorder split hand/split foot malformation type 1. In addition, it has been shown to directly interact with BRCA2. It also may play a role in the completion of the cell cycle. [provided by RefSeq, Jul 2008]
• 规格：10ul 质粒

CDS区参考序列： 点击查看序列

GGATGGGAACTGCTTCTACAGGGCCTTGGGCTATTCCTACCTGGAGTCCCTGCTGGGGAAGAGCAGGGAG

翻译后氨基酸参数序列： 点击查看序列

IFKFKERVLQTPNDLLAAGFEEHKFRNFFNAFYSVVELVEKDGSVSSLLKVFNDQSASDHIVQFLRLLTS