- accession:NM_017653
- 基因别名:DYM
- 基因描述:Homo sapiens dymeclin (DYM), mRNA.
- 载体:现货载体
- CDS区长度:2010
- 翻译后氨基酸长度:669
- 基因简介:This gene encodes a protein which is necessary for normal skeletal development and brain function. Mutations in this gene are associated with two types of recessive osteochondrodysplasia, Dyggve-Melchior-Clausen (DMC) dysplasia and Smith-McCort (SMC) dysplasia, which involve both skeletal defects and mental retardation. [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